review article | Q7318358 |
scholarly article | Q13442814 |
P50 | author | Bodo Melnik | Q88156770 |
P2860 | cites work | Crystal structure of fibroblast growth factor receptor ectodomain bound to ligand and heparin | Q24290496 |
Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome | Q24291302 | ||
Structural basis by which alternative splicing confers specificity in fibroblast growth factor receptors | Q24294933 | ||
Cellular signaling by fibroblast growth factor receptors | Q24301087 | ||
Towards dissecting the pathogenesis of retinoid-induced hair loss: all-trans retinoic acid induces premature hair follicle regression (catagen) by upregulation of transforming growth factor-beta2 in the dermal papilla | Q24305271 | ||
The effects of inflammatory cytokines on the isolated human sebaceous infundibulum | Q74440360 | ||
Activity of 5-alpha-reductase and 17-beta-hydroxysteroid dehydrogenase in the infrainfundibulum of subjects with and without acne vulgaris | Q74475218 | ||
Variation in pilosebaceous duct keratinocyte proliferation in acne patients | Q74475246 | ||
An investigation of the biology of the human sebaceous gland | Q77073637 | ||
Optimization of treatment conditions for studying the anticancer effects of retinoids using pancreatic adenocarcinoma as a model | Q77306720 | ||
Keratinocyte growth factor: a unique player in epithelial repair processes | Q77354226 | ||
Androgen responsiveness of stromal cells of the human prostate: regulation of cell proliferation and keratinocyte growth factor by androgen | Q77449351 | ||
Essential role for Sonic hedgehog during hair follicle morphogenesis | Q77771288 | ||
Synthesis and in vitro evaluation of targeted tetracycline derivatives: effects on inhibition of matrix metalloproteinases | Q79699358 | ||
Cytokeratin and filaggrin expression in nevus comedonicus | Q80026045 | ||
Acne arising in an epidermal nevus | Q81493650 | ||
Comprehensive analysis of FGF and FGFR expression in skin: FGF18 is highly expressed in hair follicles and capable of inducing anagen from telogen stage hair follicles | Q81688936 | ||
Identification of six novel autophosphorylation sites on fibroblast growth factor receptor 1 and elucidation of their importance in receptor activation and signal transduction | Q24308600 | ||
The function of KGF in morphogenesis of epithelium and reepithelialization of wounds | Q24308787 | ||
Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene | Q24324199 | ||
Insulin-like growth factor 1/insulin signaling activates androgen signaling through direct interactions of Foxo1 with androgen receptor | Q24338711 | ||
Binding of Shp2 tyrosine phosphatase to FRS2 is essential for fibroblast growth factor-induced PC12 cell differentiation | Q24522542 | ||
FRS2 alpha attenuates FGF receptor signaling by Grb2-mediated recruitment of the ubiquitin ligase Cbl. | Q24531227 | ||
FRS2 proteins recruit intracellular signaling pathways by binding to diverse targets on fibroblast growth factor and nerve growth factor receptors | Q24554326 | ||
Indian hedgehog and beta-catenin signaling: role in the sebaceous lineage of normal and neoplastic mammalian epidermis | Q24620091 | ||
Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation | Q27649204 | ||
Cell signaling by receptor tyrosine kinases | Q27860474 | ||
A lipid-anchored Grb2-binding protein that links FGF-receptor activation to the Ras/MAPK signaling pathway | Q28240585 | ||
Exocrine gland dysfunction in MC5-R-deficient mice: evidence for coordinated regulation of exocrine gland function by melanocortin peptides | Q28257807 | ||
Developmental localization of the splicing alternatives of fibroblast growth factor receptor-2 (FGFR2) | Q28263694 | ||
Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability | Q28270811 | ||
Fgf10 is essential for limb and lung formation | Q28295033 | ||
Promotion and attenuation of FGF signaling through the Ras-MAPK pathway | Q28312210 | ||
Fgfr2 is required for limb outgrowth and lung-branching morphogenesis | Q28504835 | ||
A crucial role for Fgfr2-IIIb signalling in epidermal development and hair follicle patterning | Q28508094 | ||
Role of FGF10/FGFR2b signaling during mammary gland development in the mouse embryo | Q28509412 | ||
FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development | Q28512306 | ||
Fibroblast growth factor receptor 2 tyrosine kinase is required for prostatic morphogenesis and the acquisition of strict androgen dependency for adult tissue homeostasis | Q28512592 | ||
The mouse seminal vesicle shape mutation is allelic with Fgfr2 | Q28513248 | ||
Androgen regulation of prostate morphoregulatory gene expression: Fgf10-dependent and -independent pathways | Q28564384 | ||
Heparin-binding keratinocyte growth factor is a candidate stromal-to-epithelial-cell andromedin | Q28579402 | ||
Sonic hedgehog signaling is essential for hair development | Q28586200 | ||
p63 is essential for regenerative proliferation in limb, craniofacial and epithelial development | Q28587664 | ||
Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate | Q28587665 | ||
p63 is a p53 homologue required for limb and epidermal morphogenesis | Q28588206 | ||
Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless | Q28589182 | ||
Counter-regulation of interleukin-1alpha (IL-1alpha) and IL-1 receptor antagonist in murine keratinocytes | Q40410129 | ||
Cytokine networks in the skin. | Q40447782 | ||
Sonic hedgehog induces epidermal growth factor dependent matrix infiltration in HaCaT keratinocytes. | Q40464669 | ||
Delta Np63 alpha expression is regulated by the phosphoinositide 3-kinase pathway. | Q40626867 | ||
Regulation of gli activity by all-trans retinoic acid in mouse keratinocytes. | Q40848783 | ||
IL-1 and IL-1 receptor antagonist regulation during keratinocyte cell cycle and differentiation in normal and psoriatic epidermis | Q41006746 | ||
Fibroblast-dependent induction of a murine skin lesion similar to human nevus sebaceus of Jadassohn | Q41130670 | ||
Role of transactivation of the EGF receptor in signalling by G-protein-coupled receptors | Q41229236 | ||
Keratinocyte growth factor receptor ligands induce transforming growth factor alpha expression and activate the epidermal growth factor receptor signaling pathway in cultured epidermal keratinocytes. | Q41665075 | ||
Prostatic growth and development are regulated by FGF10. | Q41679731 | ||
Accutane-exposed pregnancies--California, 1999. | Q41720266 | ||
Structure and function of the insulin-like growth factor I receptor | Q41727239 | ||
Isotretinoin-induced craniofacial malformations in humans and hamsters | Q41933662 | ||
Cooperation between sonic hedgehog and fibroblast growth factor/MAPK signalling pathways in neocortical precursors | Q42457112 | ||
Apert's syndrome and androgen receptor staining of the basal cells of sebaceous glands | Q42485989 | ||
Melanocortin-5 receptor: a marker of human sebocyte differentiation | Q42486986 | ||
Sonic hedgehog controls stem cell behavior in the postnatal and adult brain | Q42699442 | ||
Mutual induction of growth factor gene expression by epidermal-dermal cell interaction | Q42769779 | ||
SHP2 associates directly with tyrosine phosphorylated p90 (SNT) protein in FGF-stimulated cells | Q42795864 | ||
Control of fibroblast growth factor (FGF) 7- and FGF1-induced mitogenesis and downstream signaling by distinct heparin octasaccharide motifs | Q42801360 | ||
Insulin-like growth factor-1 induces lipid production in human SEB-1 sebocytes via sterol response element-binding protein-1. | Q42803798 | ||
Protein kinase C-delta and mitogen-activated protein/extracellular signal-regulated kinase-1 control GLI activation in hedgehog signaling | Q42805992 | ||
Endocytic pathways and biological effects induced by UVB-dependent or ligand-dependent activation of the keratinocyte growth factor receptor | Q42807077 | ||
Extracellular point mutations in FGFR2 elicit unexpected changes in intracellular signalling | Q42815086 | ||
Factors mediating the interactions between epidermal and dermal cells in skin grafts that might be important for hair follicle development. | Q42827983 | ||
Sprouty2 downregulation plays a pivotal role in mediating crosstalk between TGF-beta1 signaling and EGF as well as FGF receptor tyrosine kinase-ERK pathways in mesenchymal cells | Q42828139 | ||
Pronounced and early acne in Apert's syndrome: a case successfully treated with oral isotretinoin | Q44172064 | ||
Inconsistency between glycemic and insulinemic responses to regular and fermented milk products | Q44393575 | ||
Acne in Apert's syndrome: treatment with isotretinoin. | Q44440215 | ||
Proopiomelanocortin peptides and sebogenesis | Q44506898 | ||
Involvement of the SREBP pathway in the mode of action of androgens in sebaceous glands in vivo | Q44557334 | ||
Isotretinoin for acne in Apert syndrome | Q45094074 | ||
Common and distinct elements in cellular signaling via EGF and FGF receptors | Q45165242 | ||
Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling. | Q45309021 | ||
Formation of in vitro murine cleft palate by abrogation of fibroblast growth factor signaling | Q46343385 | ||
Correlation between serum levels of insulin-like growth factor 1, dehydroepiandrosterone sulfate, and dihydrotestosterone and acne lesion counts in adult women | Q46395742 | ||
Dissociation of the glycaemic and insulinaemic responses to whole and skimmed milk | Q46401809 | ||
Androgen induction of steroid 5 alpha-reductase may be mediated via insulin-like growth factor-I. | Q46543907 | ||
Role of IGFs and insulin in the human testis during postnatal activation: differentiation of steroidogenic cells | Q46562142 | ||
A pilot study to determine the short-term effects of a low glycemic load diet on hormonal markers of acne: a nonrandomized, parallel, controlled feeding trial | Q46581684 | ||
Treatment of acne with antiandrogens--an evidence-based review | Q46809999 | ||
Successful acne management in Apert syndrome twins | Q46850983 | ||
DHT and testosterone, but not DHEA or E2, differentially modulate IGF-I, IGFBP-2, and IGFBP-3 in human prostatic stromal cells | Q46861788 | ||
The fatty acid synthase gene is a conserved p53 family target from worm to human. | Q47069045 | ||
What is the pathogenesis of acne? | Q47622824 | ||
Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome. | Q47939552 | ||
Hedgehog-GLI signaling regulates the behavior of cells with stem cell properties in the developing neocortex. | Q48113249 | ||
Clinical variability in patients with Apert's syndrome | Q48269617 | ||
Apert syndrome | Q48382166 | ||
Control of sebaceous gland function in the rat by alpha-melanocyte-stimulating hormone | Q48472406 | ||
Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse | Q48837214 | ||
Convergent signalling through Fgfr2 regulates divergent craniofacial morphogenesis. | Q51830686 | ||
Correlation of facial sebum to serum insulin-like growth factor-1 in patients with acne. | Q51872307 | ||
An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. | Q52171813 | ||
Sonic hedgehog is expressed in epithelial cells during development of whisker, hair, and tooth. | Q52202976 | ||
Modelling the remission of individual acne lesions in vitro. | Q52548104 | ||
Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand | Q28609661 | ||
Protein sensors for membrane sterols | Q29617313 | ||
HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo | Q29618704 | ||
Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 and is required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4. | Q31951443 | ||
Ectopeptidases in pathophysiology | Q32063488 | ||
A quantitative study of the recruitment potential of all intracellular tyrosine residues on EGFR, FGFR1 and IGF1R. | Q33610352 | ||
Inflammatory skin disease in transgenic mice that express high levels of interleukin 1 alpha in basal epidermis | Q33730207 | ||
Gli genes in development and cancer | Q33814305 | ||
The molecular basis of lung morphogenesis | Q33855377 | ||
Soluble dominant-negative receptor uncovers essential roles for fibroblast growth factors in multi-organ induction and patterning | Q33888488 | ||
The paternal-age effect in Apert syndrome is due, in part, to the increased frequency of mutations in sperm | Q33906096 | ||
IGF-1 induces SREBP-1 expression and lipogenesis in SEB-1 sebocytes via activation of the phosphoinositide 3-kinase/Akt pathway. | Q33988649 | ||
Abuse of anabolic-androgenic steroids and bodybuilding acne: an underestimated health problem | Q34002248 | ||
Role of hormones in pilosebaceous unit development | Q34009592 | ||
Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities | Q34074836 | ||
Transducing the hedgehog signal | Q34084346 | ||
Sprouty2 inhibits the Ras/MAP kinase pathway by inhibiting the activation of Raf. | Q34100782 | ||
Testosterone formation and metabolism during male sexual differentiation in the human embryo | Q34219047 | ||
Keratins and the keratinocyte activation cycle | Q34248710 | ||
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome | Q34308670 | ||
Exclusive paternal origin of new mutations in Apert syndrome | Q34385938 | ||
13-cis Retinoic acid induces apoptosis and cell cycle arrest in human SEB-1 sebocytes | Q34507245 | ||
Inflammatory events are involved in acne lesion initiation | Q34535060 | ||
Phosphoinositide 3-kinase and Akt are essential for Sonic Hedgehog signaling | Q34574774 | ||
The effect of a high-protein, low glycemic-load diet versus a conventional, high glycemic-load diet on biochemical parameters associated with acne vulgaris: a randomized, investigator-masked, controlled trial | Q34621172 | ||
Gli and hedgehog in cancer: tumours, embryos and stem cells. | Q34665999 | ||
Retinoic acid embryopathy | Q34686260 | ||
FGF signaling pathways in endochondral and intramembranous bone development and human genetic disease | Q34702208 | ||
Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations | Q34768100 | ||
Milk consumption: aggravating factor of acne and promoter of chronic diseases of Western societies | Q34951913 | ||
Cholesterol precursors and facial clefting | Q35009494 | ||
Hormonal, cellular, and molecular control of prostatic development | Q35088639 | ||
Isotretinoin treatment of acne in a patient with Apert syndrome | Q35548282 | ||
The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development | Q35672022 | ||
Keratinocyte growth factor is an important endogenous mediator of hair follicle growth, development, and differentiation. Normalization of the nu/nu follicular differentiation defect and amelioration of chemotherapy-induced alopecia | Q35796365 | ||
Detection of interleukin-1 receptors in human epidermis. Induction of the type II receptor after organ culture and in psoriasis. | Q35834050 | ||
Hedgehog signaling regulates sebaceous gland development | Q35843342 | ||
Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome. | Q35848621 | ||
Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome | Q35881627 | ||
DeltaNp63 regulates thymic development through enhanced expression of FgfR2 and Jag2. | Q35901203 | ||
Melanocortin receptor ligands: new horizons for skin biology and clinical dermatology. | Q36567346 | ||
Regulations and roles of the interleukin-1 receptor associated kinases (IRAKs) in innate and adaptive immunity | Q36685571 | ||
p63 in skin appendage development | Q36723008 | ||
Retinoic acid induces transforming growth factor-beta 2 in cultured keratinocytes and mouse epidermis | Q36734355 | ||
Pathways of signal transduction employed by vertebrate Hedgehogs | Q36785862 | ||
Naevus comedonicus: a spectrum of body involvement | Q36825093 | ||
Keratinocyte growth factor receptors | Q36954792 | ||
Adrenarche: postnatal adrenal zonation and hormonal and metabolic regulation | Q37282192 | ||
FGFR2 signaling and the pathogenesis of acne | Q37322522 | ||
Anti-acne agents attenuate FGFR2 signal transduction in acne | Q37395769 | ||
Keratinocyte growth factor functions in epithelial induction during seminal vesicle development | Q37558690 | ||
Increased expression of protein kinase Calpha, interleukin-1alpha, and RhoA guanosine 5'-triphosphatase in osteoblasts expressing the Ser252Trp fibroblast growth factor 2 receptor Apert mutation: identification by analysis of complementary DNA micro | Q38301608 | ||
Functional analysis of the human Sprouty2 gene promoter | Q38347400 | ||
Identification of genetic pathways activated by the androgen receptor during the induction of proliferation in the ventral prostate gland. | Q38348824 | ||
Selective modulation of Hedgehog/GLI target gene expression by epidermal growth factor signaling in human keratinocytes. | Q38409513 | ||
The endocrinology and developmental biology of the prostate | Q39669602 | ||
On the role of transforming growth factor-beta in the growth inhibitory effects of retinoic acid in human pancreatic cancer cells | Q40031262 | ||
Keratinocyte growth factor receptor ligands target the receptor to different intracellular pathways. | Q40066061 | ||
Inhibitors of dipeptidyl peptidase IV and aminopeptidase N target major pathogenetic steps in acne initiation | Q40266797 | ||
Keratinocyte growth factor promotes melanosome transfer to keratinocytes | Q40340103 | ||
KGF induces lipogenic genes through a PI3K and JNK/SREBP-1 pathway in H292 cells | Q40373462 | ||
Insulin-Like Growth Factors, Insulin-Like Growth Factor Binding Proteins and Ovarian Androgen Production | Q40394429 | ||
All-trans-retinoic acid and 13-cis-retinoic acid: pharmacokinetics and biological activity in different cell culture models of human keratinocytes. | Q52927222 | ||
Polymorphisms in the human cytochrome P-450 1A1 gene (CYP1A1) as a factor for developing acne. | Q52995634 | ||
Monoclonal antibody labeling for cytokeratins and filaggrin in the human pilosebaceous unit of normal, seborrhoeic and acne skin. | Q53040934 | ||
Acne vulgaris: proliferative cells in sebaceous glands. | Q53680609 | ||
Nevus comedonicus. | Q53920930 | ||
Pro-inflammatory levels of interleukin-1 alpha-like bioactivity are present in the majority of open comedones in acne vulgaris. | Q54063556 | ||
Androgen Excess in Cystic Acne | Q54498771 | ||
Pilosebaceous abnormalities in Apert's syndrome. | Q54735805 | ||
Elevated Serum Insulin‐like Growth Factor‐1 (IGF‐1) Levels in Women with Postadolescent Acne | Q55064095 | ||
Epidermal mosaicism producing localised acne: somatic mutation in FGFR2 | Q56263112 | ||
RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis | Q56333589 | ||
What syndrome is this? Apert syndrome | Q56333904 | ||
Resolution of acne following therapy with an oral contraceptive in a patient with Apert syndrome | Q56339315 | ||
[Acrocephalosyndactyly I (Apert syndrome)] | Q56376583 | ||
Isotretinoin therapy for antibiotic-refractory acne in Apert's syndrome | Q56378982 | ||
Cutaneous manifestations of Apert syndrome | Q56384385 | ||
Apert's syndrome (acrocephalosyndactyly) in a patient with hyperhidrosis | Q56389572 | ||
Successful treatment of the acne of Apert syndrome with isotretinoin | Q56398153 | ||
The acneform eruption of Apertʼs syndrome is not acne vulgaris | Q56414698 | ||
Acneform eruption in Apert's syndrome. Acrocephalosyn dactyly | Q56417590 | ||
Apert's syndrome | Q56418184 | ||
Depigmentation of hair, skin, and eyes associated with the Apert syndrome | Q56419091 | ||
Pilosebaceous abnormalities in Apert type acrocephalosyndactyly | Q56420561 | ||
Milk consumption: aggravating factor of acne and promoter of chronic diseases of Western societies | Q56601583 | ||
Antimitochondrial effect of saturated medium chain length (C8-C13) dicarboxylic acids | Q62660086 | ||
Unilateral segmental acneiform naevus: a model disorder towards understanding fibroblast growth factor receptor 2 function in acne? | Q62661447 | ||
Interleukin 1 immunoreactivity in sebaceous glands | Q67979908 | ||
Effect of alpha-melanocyte-stimulating hormone and testosterone on cutaneous and modified sebaceous glands in the rat | Q68214377 | ||
5 alpha-dihydrotestosterone formation is necessary for embryogenesis of the rat prostate | Q68267260 | ||
Sebaceous gland response in man to the administration of testosterone, delta-4-androstenedione, and dehydroisoandrosterone | Q68426845 | ||
Cellular dynamics of comedo formation in acne vulgaris | Q68486561 | ||
Isotretinoin teratogenicity in mouse whole embryo culture | Q68727970 | ||
A longitudinal study of the relationship of plasma somatomedin-C concentration to the pubertal growth spurt | Q69009079 | ||
Androgen receptor in hirsutism and acne | Q70023786 | ||
On the mechanism of sebaceous secretion | Q70576167 | ||
Modeling acne in vitro | Q70978947 | ||
Messenger RNAs for the multifunctional cytokines interleukin-1 alpha, interleukin-1 beta and tumor necrosis factor-alpha are present in adnexal tissues and in dermis of normal human skin | Q71017789 | ||
Keratin expression in pilosebaceous epithelia in truncal skin of acne patients | Q71362738 | ||
Activity of the Type 1 5α-Reductase Exhibits Regional Differences in Isolated Sebaceous Glands and Whole Skin | Q71961324 | ||
The androgen control of sebum production. Studies of subjects with dihydrotestosterone deficiency and complete androgen insensitivity | Q72949275 | ||
c-Jun and JunB antagonistically control cytokine-regulated mesenchymal-epidermal interaction in skin | Q73291709 | ||
Interleukin-1 induces transcription of keratin K6 in human epidermal keratinocytes | Q73443704 | ||
Naevus comedonicus immunohistochemical features in two cases | Q73824992 | ||
Keratinocyte growth regulation in defined organotypic cultures through IL-1-induced keratinocyte growth factor expression in resting fibroblasts | Q73873179 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | pathogenesis | Q372016 |
P304 | page(s) | 141-156 | |
P577 | publication date | 2009-05-01 | |
P1433 | published in | Dermato-endocrinology | Q26842418 |
P1476 | title | Role of FGFR2-signaling in the pathogenesis of acne | |
P478 | volume | 1 |
Q64993941 | Acne and craniofacial defects. |
Q37825558 | Acne-associated syndromes: models for better understanding of acne pathogenesis |
Q64088373 | An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis |
Q38977482 | Beyond acne: Current aspects of sebaceous gland biology and function |
Q33727595 | Fibroblast Growth Factor Receptor 2 (FGFR2) Is Required for Meibomian Gland Homeostasis in the Adult Mouse |
Q41816222 | Generalized Comedones, Acne, and Hidradenitis Suppurativa in a Patient with an FGFR2 Missense Mutation |
Q38736949 | Genetic architecture of acne vulgaris. |
Q42704228 | Genetic research and structural dysplasia assessment of anorectal malformations in neonatal male rats induced by di(n-butyl) phthalate |
Q35558873 | Isotretinoin and FoxO1: A scientific hypothesis |
Q26800264 | Linking diet to acne metabolomics, inflammation, and comedogenesis: an update |
Q35519637 | Long-term effectiveness of dobesilate in the treatment of papulopustular rosacea |
Q54199426 | Mosaic-activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus. |
Q48416696 | Mouse models of Apert syndrome |
Q28246491 | New perspectives on antiacne plant drugs: contribution to modern therapeutics |
Q82543534 | Pathophysiological advances in acne |
Q36974479 | Photodynamic therapy inhibit Fibroblast Growth Factor-10 induced keratinocyte differentiation and proliferation through ROS in Fibroblast Growth Factor Receptor-2b pathway |
Q38191671 | The aetiopathogenesis of acne vulgaris - what's new? |
Q38262522 | The molecular and cellular basis of Apert syndrome. |
Q37149457 | The role of androgen and androgen receptor in skin-related disorders |
Q43820968 | Uncommon acne-associated syndromes and their significance in understanding the pathogenesis of acne |
Q36005424 | p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice |
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