scholarly article | Q13442814 |
P50 | author | Alberto Roselló-Díez | Q64089329 |
P2093 | author name string | Alexandra L Joyner | |
P2860 | cites work | Interaction of human suppressor of cytokine signaling (SOCS)-2 with the insulin-like growth factor-I receptor | Q24310472 |
Homozygous deletion of the human insulin receptor gene results in leprechaunism | Q24311628 | ||
LEPROT and LEPROTL1 cooperatively decrease hepatic growth hormone action in mice | Q24316352 | ||
Fibroblast growth factor receptor 3 is a negative regulator of bone growth | Q24322706 | ||
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction | Q24322907 | ||
Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation | Q24600279 | ||
Connective tissue growth factor coordinates chondrogenesis and angiogenesis during skeletal development | Q24616861 | ||
mTOR signaling in growth control and disease | Q24634174 | ||
The Hedgehog-inducible ubiquitin ligase subunit WSB-1 modulates thyroid hormone activation and PTHrP secretion in the developing growth plate | Q24669733 | ||
Glucocorticoid receptor signaling in health and disease | Q26828358 | ||
A pathway to bone: signaling molecules and transcription factors involved in chondrocyte development and maturation | Q26995910 | ||
Functions of the osteocyte network in the regulation of bone mass | Q27002647 | ||
Role of G-proteins in the differentiation of epiphyseal chondrocytes | Q27021436 | ||
Of flies, mice, and men: evolutionarily conserved tissue damage responses and aging | Q27025985 | ||
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Brain IGF-1 receptors control mammalian growth and lifespan through a neuroendocrine mechanism | Q27332330 | ||
G protein pathways | Q27919625 | ||
The effect of altering the mechanical loading environment on the expression of bone regenerating molecules in cases of distraction osteogenesis | Q28084068 | ||
Gigantism in mice lacking suppressor of cytokine signalling-2 | Q28140549 | ||
Indian hedgehog coordinates endochondral bone growth and morphogenesis via parathyroid hormone related-protein-dependent and -independent pathways | Q28142399 | ||
Growth enhancement in suppressor of cytokine signaling 2 (SOCS-2)-deficient mice is dependent on signal transducer and activator of transcription 5b (STAT5b) | Q28201918 | ||
Autoregulation of neurogenesis by GDF11 | Q28204949 | ||
BMP and Ihh/PTHrP signaling interact to coordinate chondrocyte proliferation and differentiation | Q28206100 | ||
Mechanism of thyroid hormone action | Q28217044 | ||
Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member | Q28237287 | ||
Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man | Q28248505 | ||
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. | Q52241373 | ||
Catch-up growth following illness or starvation. An example of developmental canalization in man. | Q52355018 | ||
Inducible nitric oxide synthase-nitric oxide signaling mediates the mitogenic activity of Rac1 during endochondral bone growth. | Q52616963 | ||
Neural mediation of compensatory adrenal growth | Q52711025 | ||
Morphogens, nutrients, and the basis of organ scaling. | Q52719707 | ||
Hypertrophy and unconventional cell division of hepatocytes underlie liver regeneration. | Q53165375 | ||
Reduced chondrocyte proliferation, earlier cell cycle exit and increased apoptosis in neuronal nitric oxide synthase-deficient mice. | Q53198115 | ||
Chondrocytes are released as viable cells during cartilage resorption associated with the formation of intrachondral canals in the rat tibial epiphysis. | Q53860100 | ||
Catch-up growth after prolonged hypothyroidism. | Q54149528 | ||
Calcineurin regulates coordinated outgrowth of zebrafish regenerating fins. | Q54221618 | ||
Substance P and norepinephrine modulate murine chondrocyte proliferation and apoptosis. | Q54341372 | ||
BMP-6 and BMPR-1a are up-regulated in the growth plate of the fractured tibia. | Q54475375 | ||
Women's height, reproductive success and the evolution of sexual dimorphism in modern humans. | Q55036127 | ||
Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
Multiple roles for neurofibromin in skeletal development and growth | Q56269967 | ||
Nervous and Vascular Influence on Longitudinal Growth of Bone: An Experimental Study on Rabbits | Q58276007 | ||
An In Vivo Cell Survival System Based on the Recovery of Rat Growth Cartilage from Radiation Injury | Q58980691 | ||
Canalization of Development and Genetic Assimilation of Acquired Characters | Q59065949 | ||
PTEN maintains haematopoietic stem cells and acts in lineage choice and leukaemia prevention | Q59067116 | ||
Early neonatal death in mice homozygous for a null allele of the insulin receptor gene | Q60060440 | ||
Compensation for a bad start: grow now, pay later? | Q61696600 | ||
Leptin Stimulates Parathyroid Hormone Related Peptide Expression in the Endochondral Growth Plate | Q62599243 | ||
Liver regeneration | Q63664803 | ||
Spatial and temporal regulation of GH-IGF-related gene expression in growth plate cartilage. | Q64888784 | ||
Dual and selective actions of glucocorticoids upon basal and stimulated growth hormone release in man | Q67271903 | ||
In vivo limb tissue development in the absence of nerves: a quantitative study | Q67811900 | ||
Growth enhancement of transgenic mice expressing human insulin-like growth factor I | Q67979226 | ||
Peripheral and central effects of circulating catecholamines | Q28255579 | ||
Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein | Q28281538 | ||
Smad transcription factors | Q28284775 | ||
FGF-23-Klotho signaling stimulates proliferation and prevents vitamin D-induced apoptosis | Q28289695 | ||
Myc-driven endogenous cell competition in the early mammalian embryo | Q28294348 | ||
Leptin inhibits bone formation through a hypothalamic relay: a central control of bone mass | Q28505908 | ||
PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth | Q28506149 | ||
Parathyroid hormone-related peptide delays terminal differentiation of chondrocytes during endochondral bone development | Q28507281 | ||
Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice | Q28507303 | ||
Ihh signaling is directly required for the osteoblast lineage in the endochondral skeleton | Q28508641 | ||
Ucma, a novel secreted cartilage-specific protein with implications in osteogenesis | Q28512237 | ||
Mechanical tension-stress induces expression of bone morphogenetic protein (BMP)-2 and BMP-4, but not BMP-6, BMP-7, and GDF-5 mRNA, during distraction osteogenesis | Q28566983 | ||
Connective tissue growth factor and insulin-like growth factor 2 show upregulation in early growth plate radiorecovery response following irradiation | Q28569346 | ||
Cooperative regulation of chondrocyte differentiation by CCN2 and CCN3 shown by a comprehensive analysis of the CCN family proteins in cartilage | Q28571441 | ||
Coordination of chondrogenesis and osteogenesis by fibroblast growth factor 18 | Q28584951 | ||
Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog | Q28586013 | ||
Suppression of body fat accumulation in myostatin-deficient mice | Q28586697 | ||
Dwarfism and early death in mice lacking C-type natriuretic peptide | Q28588954 | ||
Leptin regulation of bone resorption by the sympathetic nervous system and CART | Q28589974 | ||
Retinoic acid receptors are required for skeletal growth, matrix homeostasis and growth plate function in postnatal mouse | Q28591274 | ||
Mammalian Mst1 and Mst2 kinases play essential roles in organ size control and tumor suppression | Q28591557 | ||
Repression of hedgehog signaling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3 | Q28591707 | ||
Indian hedgehog stimulates periarticular chondrocyte differentiation to regulate growth plate length independently of PTHrP | Q28592577 | ||
Ucma--A novel secreted factor represents a highly specific marker for distal chondrocytes | Q28592940 | ||
FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod | Q28592971 | ||
Mechanisms limiting body growth in mammals | Q28728958 | ||
FGFR3 signaling induces a reversible senescence phenotype in chondrocytes similar to oncogene-induced premature senescence | Q28975455 | ||
Pten dependence distinguishes haematopoietic stem cells from leukaemia-initiating cells | Q29616552 | ||
Developmental regulation of the growth plate | Q29618969 | ||
Mice carrying null mutations of the genes encoding insulin-like growth factor I (Igf-1) and type 1 IGF receptor (Igf1r) | Q29619910 | ||
Role of insulin-like growth factors in embryonic and postnatal growth | Q29620034 | ||
Regulation of Hippo pathway by mitogenic growth factors via phosphoinositide 3-kinase and phosphoinositide-dependent kinase-1 | Q30417692 | ||
Postnatal growth after intrauterine growth restriction alters central leptin signal and energy homeostasis | Q31047289 | ||
Disruption of insulin-like growth factor-I expression in type IIalphaI collagen-expressing cells reduces bone length and width in mice | Q33285460 | ||
Cell lineages and the logic of proliferative control | Q33402595 | ||
Chondrocytes transdifferentiate into osteoblasts in endochondral bone during development, postnatal growth and fracture healing in mice | Q34633873 | ||
Cartilage-specific over-expression of CCN family member 2/connective tissue growth factor (CCN2/CTGF) stimulates insulin-like growth factor expression and bone growth | Q34650896 | ||
Cyclic dermal BMP signalling regulates stem cell activation during hair regeneration | Q34737529 | ||
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
Deletion of the G protein-coupled receptor 30 impairs glucose tolerance, reduces bone growth, increases blood pressure, and eliminates estradiol-stimulated insulin release in female mice | Q34849712 | ||
Endospanins regulate a postinternalization step of the leptin receptor endocytic pathway | Q34979041 | ||
The paracrine feedback loop between vitamin D₃ (1,25(OH)₂D₃) and PTHrP in prehypertrophic chondrocytes | Q34984051 | ||
Catch-up growth: definition, mechanisms, and models | Q35037999 | ||
The dangerous road of catch-up growth. | Q35058374 | ||
Return of the chalones | Q35065941 | ||
Thyroid hormone-mediated growth and differentiation of growth plate chondrocytes involves IGF-1 modulation of beta-catenin signaling | Q35069746 | ||
Chondrocyte-specific microRNA-140 regulates endochondral bone development and targets Dnpep to modulate bone morphogenetic protein signaling. | Q35096652 | ||
Nuclear factor-kappaB (NF-kappaB) p65 interacts with Stat5b in growth plate chondrocytes and mediates the effects of growth hormone on chondrogenesis and on the expression of insulin-like growth factor-1 and bone morphogenetic protein-2 | Q35107411 | ||
Preclinical studies on mesenchymal stem cell-based therapy for growth plate cartilage injury repair | Q35130994 | ||
Cellular energy stress induces AMPK-mediated regulation of YAP and the Hippo pathway | Q35236207 | ||
Distinct germline progenitor subsets defined through Tsc2-mTORC1 signaling | Q35303050 | ||
Organ-level quorum sensing directs regeneration in hair stem cell populations | Q35367291 | ||
The role of leptin in female adolescence | Q35596206 | ||
Dual pathways to endochondral osteoblasts: a novel chondrocyte-derived osteoprogenitor cell identified in hypertrophic cartilage | Q35616579 | ||
Target of rapamycin (TOR) in nutrient signaling and growth control | Q35620394 | ||
Cell polarity: The missing link in skeletal morphogenesis? | Q35624653 | ||
Insulin exerts direct, IGF-1 independent actions in growth plate chondrocytes | Q35755152 | ||
Chalones: from aqueous extracts to oligopeptides. | Q35869819 | ||
Fundamental limits on longitudinal bone growth: growth plate senescence and epiphyseal fusion. | Q35893879 | ||
A cardiac myocyte vascular endothelial growth factor paracrine pathway is required to maintain cardiac function | Q35895986 | ||
Skeletal overgrowth in transgenic mice that overexpress brain natriuretic peptide | Q35915041 | ||
Metabolic consideration of epiphyseal growth: survival responses in a taxing environment | Q35928543 | ||
Integrating body and organ size in Drosophila: recent advances and outstanding problems | Q35972040 | ||
Targeting Runx2 expression in hypertrophic chondrocytes impairs endochondral ossification during early skeletal development | Q35985042 | ||
Insulin-like growth factor ligands, receptors, and binding proteins in cancer. | Q36004697 | ||
Structural and functional properties of CCN proteins | Q36053014 | ||
Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype | Q36057344 | ||
BDNF alters ERK/p38 MAPK activity ratios to promote differentiation in growth plate chondrocytes | Q36113810 | ||
Effects of estrogen on growth plate senescence and epiphyseal fusion | Q36240179 | ||
Alterations in the growth plate associated with growth modulation by sustained compression or distraction | Q36274923 | ||
Organ size is limited by the number of embryonic progenitor cells in the pancreas but not the liver | Q34607172 | ||
Inactivation of Pten in osteo-chondroprogenitor cells leads to epiphyseal growth plate abnormalities and skeletal overgrowth | Q34622370 | ||
Hippo signaling: growth control and beyond | Q34625638 | ||
Asymmetric flies: the control of developmental noise in Drosophila. | Q34631335 | ||
Effects of early nutrition intervention on IGF1, IGFBP3, intestinal development, and catch-up growth of intrauterine growth retardation rats | Q80911605 | ||
Modulation of vertebral and tibial growth by compression loading: diurnal versus full-time loading | Q81165709 | ||
Chalones: chemical regulation of cell division | Q81192060 | ||
Thrifty metabolism that favors fat storage after caloric restriction: a role for skeletal muscle phosphatidylinositol-3-kinase activity and AMP-activated protein kinase | Q81421036 | ||
Lack of telomere shortening with age in mouse resting zone chondrocytes | Q81585060 | ||
Catch-up growth: testing the hypothesis of delayed growth plate senescence in humans | Q81630630 | ||
Bone growth in paralyzed limbs | Q82091792 | ||
Nuclear receptor-dependent bile acid signaling is required for normal liver regeneration | Q83154070 | ||
The effect of roentgen irradiation on epiphyseal growth experimental studies upon the dog | Q83283826 | ||
Role of fibroblast growth factor 21 (FGF21) in undernutrition-related attenuation of growth in mice | Q83533646 | ||
Regulative patterning in limb bud transplants is induced by distalizing activity of apical ectodermal ridge signals on host limb cells | Q83921732 | ||
Effects of hind limb unloading and reloading on nitric oxide synthase expression and apoptosis of osteocytes and chondrocytes | Q83963479 | ||
Russell–Silver syndrome | Q84966066 | ||
G protein-coupled receptors: an overview of signaling mechanisms and screening assays | Q38308895 | ||
Human leptin deficiency caused by a missense mutation: multiple endocrine defects, decreased sympathetic tone, and immune system dysfunction indicate new targets for leptin action, greater central than peripheral resistance to the effects of leptin, | Q38319405 | ||
Leptin regulates chondrocyte differentiation and matrix maturation during endochondral ossification | Q38323319 | ||
A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors | Q38329519 | ||
Leptin synergizes with thyroid hormone signaling in promoting growth plate chondrocyte proliferation and terminal differentiation in vitro | Q38337121 | ||
Organ-Size Regulation in Mammals | Q38549724 | ||
The critical role of the epidermal growth factor receptor in endochondral ossification. | Q38810753 | ||
FGF23 suppresses chondrocyte proliferation in the presence of soluble α-Klotho both in vitro and in vivo | Q39227211 | ||
YAP mediates crosstalk between the Hippo and PI(3)K–TOR pathways by suppressing PTEN via miR-29 | Q39246531 | ||
Interference by adrenaline with chondrogenic differentiation through suppression of gene transactivation mediated by Sox9 family members. | Q39506093 | ||
Hepatic branch vagotomy can suppress liver regeneration in partially hepatectomized rats | Q39665504 | ||
Telomere shortening impairs organ regeneration by inhibiting cell cycle re-entry of a subpopulation of cells | Q39804680 | ||
The Natural History of the Silver-Russell Syndrome: A Longitudinal Study of Thirty-nine Cases | Q39944787 | ||
Positional Information in Chick Limb Morphogenesis | Q39955273 | ||
Compensatory adrenal growth: a neurally mediated reflex | Q40012256 | ||
mTOR signaling contributes to chondrocyte differentiation | Q40014562 | ||
Allometry and size in ontogeny and phylogeny | Q40052889 | ||
The neural regulation of compensatory adrenal growth | Q40175848 | ||
mTORC2 regulates cardiac response to stress by inhibiting MST1. | Q40182849 | ||
The restricted potential for recovery of growth plate chondrogenesis and longitudinal bone growth following exposure to pro-inflammatory cytokines. | Q40285708 | ||
Suppressor of cytokine signaling-2 limits intestinal growth and enterotrophic actions of IGF-I in vivo | Q40297806 | ||
The cartilage specific microRNA-140 targets histone deacetylase 4 in mouse cells | Q40308810 | ||
Hormonal and nutritional regulation of IGF-I and its binding proteins | Q40397983 | ||
ACTH enhances chondrogenesis in multipotential progenitor cells and matrix production in chondrocytes. | Q40543323 | ||
Reactive oxygen species mediate Met receptor transactivation by G protein-coupled receptors and the epidermal growth factor receptor in human carcinoma cells | Q40559771 | ||
Transplantation of epiphyseal plate allografts between animals of different ages | Q40812161 | ||
The effect of anorexia nervosa and refeeding on growth hormone-binding protein, the insulin-like growth factors (IGFs), and the IGF-binding proteins | Q41093857 | ||
The role of periosteal tension in the growth of long bones | Q41450968 | ||
The bone and beyond: 'Dem bones' are made for more than walking. | Q41574661 | ||
Bioelectric signaling regulates size in zebrafish fins | Q41876070 | ||
"Dead Cells Talking": The Silent Form of Cell Death Is Not so Quiet. | Q41981106 | ||
Noncanonical frizzled signaling regulates cell polarity of growth plate chondrocytes | Q42109218 | ||
Endochondral growth in growth plates of three species at two anatomical locations modulated by mechanical compression and tension | Q42129285 | ||
Overexpression of BMP3 in the developing skeleton alters endochondral bone formation resulting in spontaneous rib fractures | Q42202564 | ||
Insulin is a mitogen for isolated epiphyseal growth plate chondrocytes from the fetal lamb | Q42481155 | ||
IGF and IGF-binding protein expression in the growth plate of normal, dexamethasone-treated and human IGF-II transgenic mice | Q42526869 | ||
The Growth in Length of the Long Bones in the Madder-fed Pig. | Q42561938 | ||
β2-adrenergic receptors inhibit the expression of collagen type II in growth plate chondrocytes by stimulating the AP-1 factor Jun-B. | Q42774029 | ||
Regulation of chick bone growth by leptin and catecholamines | Q43121762 | ||
Patterns of catch-up growth | Q43478556 | ||
Highly activated Fgfr3 with the K644M mutation causes prolonged survival in severe dwarf mice | Q43640386 | ||
Bone phenotype of the aromatase deficient mouse | Q43890518 | ||
Osteocytic canalicular networks: morphological implications for altered mechanosensitivity | Q43995302 | ||
Rickets in VDR null mice is secondary to decreased apoptosis of hypertrophic chondrocytes | Q44112941 | ||
Cartilage sulfation during catch-up growth after fasting in rats | Q44136007 | ||
Interaction of FGF, Ihh/Pthlh, and BMP signaling integrates chondrocyte proliferation and hypertrophic differentiation | Q44166152 | ||
Runx2 expression and action in chondrocytes are regulated by retinoid signaling and parathyroid hormone-related peptide (PTHrP). | Q44264957 | ||
Regulation by growth hormone of number of chondrocytes containing IGF-I in rat growth plate | Q44327491 | ||
Increased bone mass, altered trabecular architecture and modified growth plate organization in the growing skeleton of SOCS2 deficient mice. | Q44357317 | ||
Molecular pathways mediating mechanical signaling in bone | Q36345286 | ||
Liver-derived insulin-like growth factor I (IGF-I) is the principal source of IGF-I in blood but is not required for postnatal body growth in mice | Q36392687 | ||
Normal growth and development in the absence of hepatic insulin-like growth factor I | Q36394699 | ||
Vitamin D physiology | Q36430932 | ||
IGF-1R signaling in chondrocytes modulates growth plate development by interacting with the PTHrP/Ihh pathway | Q36488507 | ||
Targeted ablation of the vitamin D receptor: an animal model of vitamin D-dependent rickets type II with alopecia | Q36576317 | ||
Development of the endochondral skeleton | Q36629738 | ||
BMP signaling in the cartilage growth plate. | Q36659526 | ||
Thyroid hormone and the growth plate | Q36698197 | ||
Cytokine receptor signaling through the Jak-Stat-Socs pathway in disease. | Q36701486 | ||
Multiple phases of chondrocyte enlargement underlie differences in skeletal proportions | Q36711346 | ||
Role of CCN2/CTGF/Hcs24 in bone growth | Q36729090 | ||
Small for gestational age: short stature and beyond | Q36745231 | ||
Roles of epidermal growth factor family in the regulation of postnatal somatic growth. | Q36745234 | ||
An imprinted gene network that controls mammalian somatic growth is down-regulated during postnatal growth deceleration in multiple organs | Q36808158 | ||
Expression of multiple insulin and insulin-like growth factor receptor genes in salmon gill cartilage | Q36816503 | ||
Size and shape: the developmental regulation of static allometry in insects. | Q36824800 | ||
Histomorphometric evidence of growth plate recovery potential after fractionated radiotherapy: an in vivo model | Q36916881 | ||
Mitogenic signaling pathways induced by G protein-coupled receptors | Q36929839 | ||
The growth hormone-insulin-like growth factor-I axis in chronic kidney disease | Q36934464 | ||
Inhibition of growth hormone signaling by the fasting-induced hormone FGF21. | Q36953853 | ||
Endocrine functions of bone in mineral metabolism regulation. | Q36982323 | ||
FGFR3 and FGFR4 do not mediate renal effects of FGF23. | Q36985772 | ||
GPCR-jacking: from a new route in RTK signalling to a new concept in GPCR activation | Q37000953 | ||
Insulin-like growth factor-binding proteins and bone metabolism | Q37001115 | ||
Natriuretic peptide C receptor signalling in the heart and vasculature | Q37002318 | ||
CCN2/CTGF is required for matrix organization and to protect growth plate chondrocytes from cellular stress | Q37004735 | ||
In vivo genetic evidence for klotho-dependent, fibroblast growth factor 23 (Fgf23) -mediated regulation of systemic phosphate homeostasis | Q37072412 | ||
Roles of Wnt signalling in bone growth, remodelling, skeletal disorders and fracture repair. | Q37076212 | ||
Myostatin (GDF-8) inhibits chondrogenesis and chondrocyte proliferation in vitro by suppressing Sox-9 expression | Q37081618 | ||
Contrasting bone effects of temporary versus permanent IGFBP administration in rodents | Q37097561 | ||
Leptin and regulation of linear growth | Q37135141 | ||
An extensive genetic program occurring during postnatal growth in multiple tissues | Q37136956 | ||
let-7 and miR-140 microRNAs coordinately regulate skeletal development. | Q37143645 | ||
Iodothyronine deiodinase enzyme activities in bone. | Q37189394 | ||
SCF, BDNF, and Gas6 are regulators of growth plate chondrocyte proliferation and differentiation | Q33576515 | ||
Phosphoinositide-dependent kinase 1 and mTORC2 synergistically maintain postnatal heart growth and heart function in mice | Q33602622 | ||
Neuroendocrine control of growth hormone secretion | Q33604638 | ||
mTOR regulation and therapeutic rejuvenation of aging hematopoietic stem cells | Q33609242 | ||
Compensatory cellular hypertrophy: the other strategy for tissue homeostasis. | Q33616271 | ||
Growth retardation in children with chronic renal failure | Q33734624 | ||
Some Unexpected Results of the Heteroplastic Transplantation of Limbs | Q33763581 | ||
Regulation by fasting of rat insulin-like growth factor I and its receptor. Effects on gene expression and binding | Q33848600 | ||
MicroRNA-140 plays dual roles in both cartilage development and homeostasis | Q33885698 | ||
Disruption of the p70(s6k)/p85(s6k) gene reveals a small mouse phenotype and a new functional S6 kinase | Q33890035 | ||
Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis | Q33902251 | ||
Genetic disorders of the skeleton: a developmental approach | Q33906292 | ||
Distribution of slow-cycling cells in epiphyseal cartilage and requirement of β-catenin signaling for their maintenance in growth plate | Q33964899 | ||
Catch-up growth: possible mechanisms | Q33982207 | ||
Is bone a target-tissue for the nervous system? New advances on the understanding of their interactions | Q33997030 | ||
Coordinated postnatal down-regulation of multiple growth-promoting genes: evidence for a genetic program limiting organ growth. | Q34017146 | ||
Conditional deletion of insulin-like growth factor-I in collagen type 1alpha2-expressing cells results in postnatal lethality and a dramatic reduction in bone accretion | Q34046618 | ||
Hypertrophic chondrocytes can become osteoblasts and osteocytes in endochondral bone formation | Q34083023 | ||
mTOR mediates Wnt-induced epidermal stem cell exhaustion and aging. | Q34129574 | ||
The somatomedin hypothesis: 2001. | Q34131694 | ||
G-protein stimulatory subunit alpha and Gq/11α G-proteins are both required to maintain quiescent stem-like chondrocytes | Q34132200 | ||
GPR30 deficiency causes increased bone mass, mineralization, and growth plate proliferative activity in male mice | Q34132870 | ||
Leptin regulates bone formation via the sympathetic nervous system | Q34157988 | ||
Height and occupational success: a review and critique | Q34173315 | ||
MiR-365: a mechanosensitive microRNA stimulates chondrocyte differentiation through targeting histone deacetylase 4. | Q34209593 | ||
Endogenous retinoids in mammalian growth plate cartilage: analysis and roles in matrix homeostasis and turnover | Q34299146 | ||
The effect of physical height on workplace success and income: preliminary test of a theoretical model | Q34322798 | ||
Nutritional regulation of the insulin-like growth factors | Q34339433 | ||
Mechanical activation of mammalian target of rapamycin pathway is required for cartilage development | Q34365539 | ||
Multiple melanocortin receptors are expressed in bone cells | Q34408083 | ||
The Fibroblast Growth Factor signaling pathway | Q34467171 | ||
A review of crosstalk between MAPK and Wnt signals and its impact on cartilage regeneration | Q34527178 | ||
Insight into the physiological actions of thyroid hormone receptors from genetically modified mice | Q34529692 | ||
Increased expression of fibroblast growth factor 21 (FGF21) during chronic undernutrition causes growth hormone insensitivity in chondrocytes by inducing leptin receptor overlapping transcript (LEPROT) and leptin receptor overlapping transcript-like | Q37189525 | ||
Tamoxifen-inducible gene deletion reveals a distinct cell type associated with trabecular bone, and direct regulation of PTHrP expression and chondrocyte morphology by Ihh in growth region cartilage. | Q37199110 | ||
Tyrosine phosphorylation controls Runx2-mediated subnuclear targeting of YAP to repress transcription | Q37259684 | ||
Striking the balance between PTEN and PDK1: it all depends on the cell context | Q37287601 | ||
Thyroid hormone actions in cartilage and bone | Q37290960 | ||
Signaling cross-talk between TGF-beta/BMP and other pathways | Q37323342 | ||
Lkb1/Stk11 regulation of mTOR signaling controls the transition of chondrocyte fates and suppresses skeletal tumor formation | Q37352985 | ||
Inflammatory cytokines and the GH/IGF-I axis: novel actions on bone growth. | Q37426523 | ||
Signaling networks and transcription factors regulating mechanotransduction in bone | Q37483735 | ||
Thrifty metabolic programming in rats is induced by both maternal undernutrition and postnatal leptin treatment, but masked in the presence of both: implications for models of developmental programming. | Q37506844 | ||
Genetic control of bone formation | Q37540138 | ||
Hedgehog target genes: mechanisms of carcinogenesis induced by aberrant hedgehog signaling activation | Q37622323 | ||
A functional interaction between Hippo-YAP signalling and FoxO1 mediates the oxidative stress response. | Q37656609 | ||
Critical roles of the guanylyl cyclase B receptor in endochondral ossification and development of female reproductive organs | Q37693870 | ||
Wnt and the Wnt signaling pathway in bone development and disease | Q37724188 | ||
Natriuretic peptide system: an overview of studies using genetically engineered animal models | Q37863198 | ||
Receptor tyrosine kinase-G-protein-coupled receptor signalling platforms: out of the shadow? | Q37879733 | ||
Endocrine regulation of longitudinal bone growth | Q37922021 | ||
Molecular defects causing skeletal dysplasias | Q37922025 | ||
Inflammation and linear bone growth: the inhibitory role of SOCS2 on GH/IGF-1 signaling. | Q38034072 | ||
Fibroblast growth factor 21 as an emerging metabolic regulator: clinical perspectives. | Q38058339 | ||
The Hippo superhighway: signaling crossroads converging on the Hippo/Yap pathway in stem cells and development | Q38073434 | ||
The Hippo pathway: regulators and regulations | Q38083640 | ||
Beckwith-Wiedemann and Silver-Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth | Q38089794 | ||
The paradox of FGFR3 signaling in skeletal dysplasia: why chondrocytes growth arrest while other cells over proliferate. | Q38167936 | ||
Retinoic acid signaling pathways in development and diseases | Q38176138 | ||
A new mechanism for growth hormone receptor activation of JAK2, and implications for related cytokine receptors | Q38237652 | ||
Intracellular signaling mechanisms of the melanocortin receptors: current state of the art. | Q38287475 | ||
TGFbeta and PTHrP control chondrocyte proliferation by activating cyclin D1 expression. | Q38294039 | ||
Leptin is a potent stimulator of bone growth in ob/ob mice | Q38307707 | ||
Paralysis and growth of the musculoskeletal system in the embryonic chick | Q68613395 | ||
Effect of peripheral nerve on limb development | Q68833174 | ||
Studies of long bone growth. I. Determination of differential elongation in paired growth plates of the rat | Q68867881 | ||
Periosteal division and longitudinal growth in the tibia of the rat | Q69447961 | ||
Effect of denervation on limb growth | Q69735907 | ||
Differential expression of insulin-like growth factor-I (IGF-I) and IGF-II messenger ribonucleic acid in growing rat bone | Q70577706 | ||
Determination of proliferative characteristics of growth plate chondrocytes by labeling with bromodeoxyuridine | Q70586359 | ||
Catch-up growth | Q71086005 | ||
Cell cycle analysis of proliferative zone chondrocytes in growth plates elongating at different rates | Q71420377 | ||
Control of the limb bud outgrowth in quail-chick chimera | Q71959161 | ||
The effect of experimental epiphysiodesis on growth in length of the rabbit's tibia | Q72047802 | ||
Beta-receptor blockade by propranolol modifies the effect of the inhibitory, endogenous epidermal pentapeptide on epidermal cell flux at the G2-M transition but not at the G1-S transition | Q72456506 | ||
Longitudinal overgrowth of bone after osteotomy in young rats: influence of bone stability | Q73166922 | ||
Expression of cyclin-dependent kinase inhibitors in epiphyseal chondrocytes induced to terminally differentiate with thyroid hormone | Q73274536 | ||
Evaluation of apoptosis and the glucocorticoid receptor in the cartilage growth plate and metaphyseal bone cells of rats after high-dose treatment with corticosterone | Q73315959 | ||
Localization of estrogen receptors-alpha and -beta and androgen receptor in the human growth plate at different pubertal stages | Q73375829 | ||
Short-term glucocorticoid treatment of prepubertal mice decreases growth and IGF-I expression in the growth plate | Q73448977 | ||
Interaction of epidermal growth factor and insulin-like growth factor-I in the regulation of growth plate chondrocytes | Q73510850 | ||
The localization of androgen receptors in human bone | Q73785087 | ||
Catch-up growth | Q73790897 | ||
Indian hedgehog is an essential component of mechanotransduction complex to stimulate chondrocyte proliferation | Q74244069 | ||
Gender differences in expression of androgen receptor in tibial growth plate and metaphyseal bone of the rat | Q74252553 | ||
Serum leptin concentrations during pregnancy and their relationship to fetal growth | Q74277329 | ||
Modulation of appositional and longitudinal bone growth in the rat ulna by applied static and dynamic force | Q74363726 | ||
Testosterone stimulates insulin-like growth factor-I and insulin-like growth factor-I-receptor gene expression in the mandibular condyle--a model of endochondral ossification | Q74657626 | ||
Sex steroid metabolism in the tibial growth plate of the rat | Q74805683 | ||
Overexpression of CNP in chondrocytes rescues achondroplasia through a MAPK-dependent pathway | Q75217684 | ||
THE AUTONOMOUS BEHAVIOUR OF NORMAL THYMUS GRAFTS | Q76544878 | ||
RESTRICTED GROWTH CAPACITY OF MULTIPLE SPLEEN GRAFTS | Q76805534 | ||
REGULATION OF THE LONGITUDINAL GROWTH OF LONG BONES | Q76814705 | ||
The effects of dynamic axial loading on the rat growth plate | Q77547301 | ||
Recovery of liver mass without proliferation of hepatocytes after partial hepatectomy in Skp2-deficient mice | Q77678637 | ||
Genetics of mouse growth | Q77684683 | ||
Adrenocorticotropin insensitivity syndromes | Q77712276 | ||
Expression of thyroid hormone receptor isoforms in rat growth plate cartilage in vivo | Q78197613 | ||
The effects of the estrogen receptor blocker, Faslodex (ICI 182,780), on estrogen-accelerated bone maturation in mice | Q78206740 | ||
Enlargement of growth plate chondrocytes modulated by sustained mechanical loading | Q78366827 | ||
REGULATION OF EXCESSES AND DEFICIENCIES OF THE WING RUDIMENT OF THE CHICK EMBRYO | Q78373278 | ||
Changes of bone morphology in response to hindlimb suspension of rats | Q79367619 | ||
Nosology and classification of genetic skeletal disorders: 2006 revision | Q79375682 | ||
Rapamycin retards growth and causes marked alterations in the growth plate of young rats | Q79977811 | ||
Restoration of growth plate function following radiotherapy is driven by increased proliferative and synthetic activity of expansions of chondrocytic clones | Q80135980 | ||
Smad4 is required for the normal organization of the cartilage growth plate | Q80383784 | ||
Serum leptin concentrations in children with mild protein-energy malnutrition and catch-up growth | Q80877338 | ||
Dexamethasone increases growth hormone receptor messenger ribonucleic acid levels in liver and growth plate. | Q52214434 | ||
SOCS2 is the critical regulator of GH action in murine growth plate chondrogenesis | Q44677007 | ||
Temporal changes in PTHrP, Bcl-2, Bax, caspase, TGF-beta, and FGF-2 expression following growth plate irradiation with or without radioprotectant | Q44733049 | ||
Inactivation of the 25-hydroxyvitamin D 1alpha-hydroxylase and vitamin D receptor demonstrates independent and interdependent effects of calcium and vitamin D on skeletal and mineral homeostasis | Q44739140 | ||
The sequence of the hemoregulatory peptide is present in Gi alpha proteins | Q44810124 | ||
Minutes: Mutants of Drosophila autonomously affecting cell division rate | Q44889355 | ||
Serum somatomedin stimulation in thyroxine-treated hypophysectomized rats | Q45261991 | ||
BMPs regulate multiple aspects of growth-plate chondrogenesis through opposing actions on FGF pathways. | Q45958669 | ||
Chondrocyte-specific modulation of Cyp27b1 expression supports a role for local synthesis of 1,25-dihydroxyvitamin D3 in growth plate development. | Q45991856 | ||
Natural large-scale regeneration of rib cartilage in a mouse model. | Q45999374 | ||
Neuromedin-U inhibits unilateral adrenalectomy-induced compensatory adrenal growth in the rat. | Q46018386 | ||
Effect of fasting on insulin-like growth factor-I (IGF-I) and growth hormone receptor mRNA levels and IGF-I gene transcription in rat liver | Q46112882 | ||
The role of the G protein-coupled receptor GPR30 in the effects of estrogen in ovariectomized mice | Q46195070 | ||
Autonomic regulation of liver regeneration after partial hepatectomy in mice | Q46487611 | ||
Retinoic acid in development: towards an integrated view | Q46549138 | ||
Peroxisome proliferator activated receptor-gamma (PPARgamma) represses thyroid hormone signaling in growth plate chondrocytes | Q46603665 | ||
MITOTIC CONTROL BY INTERNAL SECRETION: THE ROLE OF THE CHALONE-ADRENALIN COMPLEX. | Q46663624 | ||
Endocrine profile of children with intrauterine growth retardation | Q46674606 | ||
Beta2-adrenergic receptors expressed on murine chondrocytes stimulate cellular growth and inhibit the expression of Indian hedgehog and collagen type X. | Q46866359 | ||
Secreted peptide Dilp8 coordinates Drosophila tissue growth with developmental timing. | Q47072280 | ||
Imaginal discs secrete insulin-like peptide 8 to mediate plasticity of growth and maturation. | Q47072549 | ||
A longitudinal study of the growth of the New Zealand white rabbit: cumulative and biweekly incremental growth rates for body length, body weight, femoral length, and tibial length | Q47214931 | ||
Insulin-like growth factor-I and growth in height, leg length, and trunk length between ages 5 and 10 years | Q47339180 | ||
REGULATION OF GROWTH IN SIZE IN MAMMALS. | Q47423890 | ||
Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds | Q47645757 | ||
Age- and site-specific decline in insulin-like growth factor-I receptor expression is correlated with differential growth plate activity in the mouse hindlimb | Q47785593 | ||
Central nervous system-specific knockout of Brg1 causes growth retardation and neuronal degeneration | Q48099697 | ||
Catch-up growth follows an abnormal pattern in experimental renal insufficiency and growth hormone treatment normalizes it. | Q48428205 | ||
Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. | Q49042849 | ||
Cell competition promotes phenotypically silent cardiomyocyte replacement in the mammalian heart. | Q50449935 | ||
Shifting linear growth during infancy: illustration of genetic factors in growth from fetal life through infancy. | Q50918879 | ||
Epiphyseal growth plate growth hormone receptor signaling is decreased in chronic kidney disease-related growth retardation. | Q50954759 | ||
Leptin reverses the inhibitory effect of caloric restriction on longitudinal growth. | Q51534065 | ||
Effects of prolonged food deprivation on the ultradian growth hormone rhythm and immunoreactive somatostatin tissue levels in the rat | Q51662299 | ||
Role of IGF signaling in catch-up growth and accelerated temporal development in zebrafish embryos in response to oxygen availability. | Q51890344 | ||
Depletion of resting zone chondrocytes during growth plate senescence. | Q52020770 | ||
Growth plate senescence is associated with loss of DNA methylation. | Q52045016 | ||
Evidence supporting dual, IGF-I-independent and IGF-I-dependent, roles for GH in promoting longitudinal bone growth. | Q52093861 | ||
The hypothalamic insulin-like growth factor-1 receptor and its relationship to gonadotropin-releasing hormones neurones during postnatal development. | Q52093909 | ||
Wnt5a and Wnt5b exhibit distinct activities in coordinating chondrocyte proliferation and differentiation. | Q52110044 | ||
Catch-up growth is associated with delayed senescence of the growth plate in rabbits. | Q52128408 | ||
Expression of aromatase in the human growth plate. | Q52129401 | ||
Roles of growth hormone and insulin-like growth factor 1 in mouse postnatal growth. | Q52142765 | ||
Thyroid hormones regulate hypertrophic chondrocyte differentiation and expression of parathyroid hormone-related peptide and its receptor during endochondral bone formation. | Q52143090 | ||
A neonatal lethal mutation in FGFR3 uncouples proliferation and differentiation of growth plate chondrocytes in embryos. | Q52167503 | ||
Igf1 promotes longitudinal bone growth by insulin-like actions augmenting chondrocyte hypertrophy. | Q52173480 | ||
Growth-promoting interaction of IGF-II with the insulin receptor during mouse embryonic development. | Q52192889 | ||
The developmental skeletal growth in the rat foot is reduced after denervation. | Q52194325 | ||
Fetal insulin-like growth factor (IGF)-I and IGF-II are regulated differently by glucose or insulin in the sheep fetus. | Q52203848 | ||
Cellular patterns of insulin-like growth factor system gene expression in murine chondrogenesis and osteogenesis. | Q52207923 | ||
Catch-up growth after glucocorticoid excess: a mechanism intrinsic to the growth plate. | Q52213846 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 646-680 | |
P577 | publication date | 2015-10-20 | |
P1433 | published in | Endocrine Reviews | Q3054007 |
P1476 | title | Regulation of Long Bone Growth in Vertebrates; It Is Time to Catch Up | |
P478 | volume | 36 |
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