review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Benoît Robert | |
Yvan Lallemand | |||
P2860 | cites work | Control of Hoxd genes' collinearity during early limb development | Q82202978 |
Axial and paraxial influences on limb morphogenesis | Q88980341 | ||
Sonic Hedgehog-induced activation of the Gli1 promoter is mediated by GLI3 | Q22009022 | ||
Hedgehog-regulated processing of Gli3 produces an anterior/posterior repressor gradient in the developing vertebrate limb | Q22253250 | ||
A global control region defines a chromosomal regulatory landscape containing the HoxD cluster | Q24301317 | ||
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly | Q24530593 | ||
Proteolytic processing yields two secreted forms of sonic hedgehog | Q24652623 | ||
Mutual genetic antagonism involving GLI3 and dHAND prepatterns the vertebrate limb bud mesenchyme prior to SHH signaling | Q24672542 | ||
Generalized lacZ expression with the ROSA26 Cre reporter strain | Q27860837 | ||
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly | Q28184095 | ||
Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse | Q28204667 | ||
Manifestation of the limb prepattern: limb development in the absence of sonic hedgehog function | Q28209365 | ||
Fibroblast growth factors induce additional limb development from the flank of chick embryos | Q28236232 | ||
Phylogenetic conservation of a limb-specific, cis-acting regulator of Sonic hedgehog ( Shh) | Q28239036 | ||
A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene | Q28263330 | ||
Identification of a palmitic acid-modified form of human Sonic hedgehog | Q28271228 | ||
Resynthesizing evolutionary and developmental biology | Q28276409 | ||
Evidence for an expansion-based temporal Shh gradient in specifying vertebrate digit identities | Q28277481 | ||
Morphogens, compartments, and pattern: lessons from drosophila? | Q28282905 | ||
The microRNA miR-196 acts upstream of Hoxb8 and Shh in limb development | Q28284609 | ||
Signaling from Smo to Ci/Gli: conservation and divergence of Hedgehog pathways from Drosophila to vertebrates | Q28285927 | ||
Retinoic acid is required for the initiation of outgrowth in the chick limb bud | Q28289746 | ||
Cholesterol modification of hedgehog signaling proteins in animal development | Q28291005 | ||
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function | Q28291924 | ||
Dynamic changes in the response of cells to positive hedgehog signaling during mouse limb patterning | Q28504770 | ||
Evidence for genetic control of Sonic hedgehog by Gli3 in mouse limb development | Q28505407 | ||
Gremlin-mediated BMP antagonism induces the epithelial-mesenchymal feedback signaling controlling metanephric kidney and limb organogenesis | Q28506504 | ||
Gremlin is the BMP antagonist required for maintenance of Shh and Fgf signals during limb patterning | Q28507504 | ||
All mouse ventral spinal cord patterning by hedgehog is Gli dependent and involves an activator function of Gli3 | Q28508067 | ||
Targeted inactivation of Hoxb8 affects survival of a spinal ganglion and causes aberrant limb reflexes | Q28508096 | ||
Tbx2 is essential for patterning the atrioventricular canal and for morphogenesis of the outflow tract during heart development | Q28508308 | ||
Tbx5 and Tbx4 are not sufficient to determine limb-specific morphologies but have common roles in initiating limb outgrowth | Q28508863 | ||
Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome | Q28509247 | ||
Cholesterol modification of sonic hedgehog is required for long-range signaling activity and effective modulation of signaling by Ptc1 | Q28509262 | ||
Analysis of Msx1; Msx2 double mutants reveals multiple roles for Msx genes in limb development | Q28509748 | ||
Retinoic acid synthesis controlled by Raldh2 is required early for limb bud initiation and then later as a proximodistal signal during apical ectodermal ridge formation | Q28586351 | ||
Some distal limb structures develop in mice lacking Sonic hedgehog signaling | Q28587394 | ||
Mouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expression | Q28588797 | ||
Multiple roles of Hoxa11 and Hoxd11 in the formation of the mammalian forelimb zeugopod | Q28591217 | ||
Hedgehog signalling in the mouse requires intraflagellar transport proteins | Q28593010 | ||
Dispatched, a novel sterol-sensing domain protein dedicated to the release of cholesterol-modified hedgehog from signaling cells | Q28609755 | ||
Sonic hedgehog mediates the polarizing activity of the ZPA | Q29616565 | ||
Positional information and the spatial pattern of cellular differentiation | Q29616635 | ||
Hox genes in digit development and evolution | Q33592049 | ||
Fibroblast-growth-factor-induced additional limbs in the study of initiation of limb formation, limb identity, myogenesis, and innervation | Q33592062 | ||
Engineering the mouse genome by site-specific recombination | Q33744862 | ||
Finding the genes that direct mammalian development : ENU mutagenesis in the mouse. | Q33846531 | ||
Signal relay by BMP antagonism controls the SHH/FGF4 feedback loop in vertebrate limb buds. | Q33877368 | ||
Shh and Gli3 are dispensable for limb skeleton formation but regulate digit number and identity | Q34146314 | ||
Organizing axes in time and space; 25 years of colinear tinkering | Q34215299 | ||
Local application of retinoic acid to the limb bond mimics the action of the polarizing region | Q34277958 | ||
Finger or toe: the molecular basis of limb identity | Q34281744 | ||
Limb-patterning activity and restricted posterior localization of the amino-terminal product of Sonic hedgehog cleavage. | Q34297272 | ||
A positive feedback loop coordinates growth and patterning in the vertebrate limb. | Q34324097 | ||
Mouse Disp1 is required in sonic hedgehog-expressing cells for paracrine activity of the cholesterol-modified ligand | Q34372957 | ||
"Fingering" the vertebrate limb | Q34499173 | ||
Morpho-regulation of ectodermal organs: integument pathology and phenotypic variations in K14-Noggin engineered mice through modulation of bone morphogenic protein pathway | Q35096113 | ||
Protein kinase A directly regulates the activity and proteolysis of cubitus interruptus | Q35915402 | ||
The developing limb and the control of the number of digits | Q36023736 | ||
Developmental regulation of the Hox genes during axial morphogenesis in the mouse | Q36156226 | ||
Regulation of Cre recombinase activity by mutated estrogen receptor ligand-binding domains | Q38343320 | ||
Interdigital regulation of digit identity and homeotic transformation by modulated BMP signaling | Q39542358 | ||
The Wnt antagonist Dickkopf-1 is regulated by Bmp signaling and c-Jun and modulates programmed cell death | Q39646720 | ||
Site-specific recombinases: tools for genome engineering. | Q40721692 | ||
The world according to hedgehog | Q40915522 | ||
Function of homeobox genes in skeletal development | Q41029846 | ||
Developmental functions of mammalian Hox genes | Q41547501 | ||
Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development | Q41734974 | ||
The chick oligozeugodactyly (ozd) mutant lacks sonic hedgehog function in the limb | Q44254913 | ||
Proteolysis That Is Inhibited by Hedgehog Targets Cubitus interruptus Protein to the Nucleus and Converts It to a Repressor | Q44894172 | ||
Roles for FGF8 in the induction, initiation, and maintenance of chick limb development | Q46448253 | ||
Eyes absent, a key repressor of polar cell fate during Drosophila oogenesis | Q47072399 | ||
Evidence of a role for T-box genes in the evolution of limb morphogenesis and the specification of forelimb/hindlimb identity | Q47176645 | ||
A dual role for Hox genes in limb anterior-posterior asymmetry | Q47358694 | ||
Direct interaction with Hoxd proteins reverses Gli3-repressor function to promote digit formation downstream of Shh. | Q47719346 | ||
Function of BMPs in the apical ectoderm of the developing mouse limb | Q47774270 | ||
Mouse Dispatched homolog1 is required for long-range, but not juxtacrine, Hh signaling | Q48279054 | ||
Genomic regulation of Hox collinearity. | Q52029359 | ||
Early developmental arrest of mammalian limbs lacking HoxA/HoxD gene function. | Q52046374 | ||
Tbx3 can alter limb position along the rostrocaudal axis of the developing embryo. | Q52054111 | ||
Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb. | Q52059096 | ||
Single base pair change in the long-range Sonic hedgehog limb-specific enhancer is a genetic basis for preaxial polydactyly. | Q52060924 | ||
Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development. | Q52088155 | ||
The limb bud Shh-Fgf feedback loop is terminated by expansion of former ZPA cells. | Q52088637 | ||
Tbx Genes Specify Posterior Digit Identity through Shh and BMP Signaling. | Q52095015 | ||
Fgf signaling controls the number of phalanges and tip formation in developing digits. | Q52099058 | ||
Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs. | Q52112403 | ||
Regulation of Tbx3 expression by anteroposterior signalling in vertebrate limb development. | Q52113875 | ||
In vivo evidence that BMP signaling is necessary for apoptosis in the mouse limb. | Q52115127 | ||
Progression of vertebrate limb development through SHH-mediated counteraction of GLI3. | Q52115170 | ||
Hox9 genes and vertebrate limb specification. | Q52195016 | ||
Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse. | Q52196441 | ||
Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls. | Q52201020 | ||
Ectopic expression of Hoxb-8 causes duplication of the ZPA in the forelimb and homeotic transformation of axial structures. | Q52215001 | ||
Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutant extra toes (Xt) | Q57927095 | ||
Sonic hedgehog and Fgf-4 act through a signaling cascade and feedback loop to integrate growth and patterning of the developing limb bud | Q58198494 | ||
Coordinate expression of the murine Hox-5 complex homoeobox-containing genes during limb pattern formation | Q59065602 | ||
Engineering chromosomes in mice through targeted meiotic recombination (TAMERE) | Q59986797 | ||
A duplicated zone of polarizing activity in polydactylous mouse mutants | Q71941033 | ||
Limb initiation and development is normal in the absence of the mesonephros | Q73702375 | ||
P433 | issue | 9 | |
P304 | page(s) | 2337-2352 | |
P577 | publication date | 2006-09-01 | |
P1433 | published in | Developmental Dynamics | Q59752 |
P1476 | title | Anteroposterior patterning in the limb and digit specification: contribution of mouse genetics | |
P478 | volume | 235 |
Q41903862 | A unique protection signal in Cubitus interruptus prevents its complete proteasomal degradation |
Q34370374 | Analysis of hedgehog signaling in mouse intraflagellar transport mutants |
Q39300951 | Anterior-posterior differences in HoxD chromatin topology in limb development |
Q34575070 | BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb development |
Q24644467 | Canine polydactyl mutations with heterogeneous origin in the conserved intronic sequence of LMBR1 |
Q46600830 | Cis-regulatory underpinnings of human GLI3 expression in embryonic craniofacial structures and internal organs. |
Q58642322 | Finger, Sex, and Side Differences in Fingertip Size and Lack of Association with Image-Based Digit Ratio (2D:4D) Measurements |
Q37779763 | Genetic and pathologic aspects of retinoic acid-induced limb malformations in the mouse |
Q28751283 | Hoxb5b acts downstream of retinoic acid signaling in the forelimb field to restrict heart field potential in zebrafish |
Q33281754 | Human GLI3 intragenic conserved non-coding sequences are tissue-specific enhancers |
Q33567281 | Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development |
Q28592776 | Identification and analysis of a conserved Tcfap2a intronic enhancer element required for expression in facial and limb bud mesenchyme |
Q36173741 | Identification and functional characterization of novel transcriptional enhancers involved in regulating human GLI3 expression during early development. |
Q28472496 | Identification of a novel retinoid by small molecule screening with zebrafish embryos |
Q39525476 | Inhibition of Pancreatic Cancer Cell-Induced Paracrine Hedgehog Signaling by Liver X Receptor Agonists and Oxy16, a Naturally Occurring Oxysterol. |
Q34041473 | Molecular genetics of Müllerian duct formation, regression and differentiation |
Q47073672 | Morphology of pelvic fin loss in a zebrafish strain (Danio rerio). |
Q28507114 | Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway |
Q37036052 | Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis |
Q37369781 | Negative regulation of Hedgehog signaling by liver X receptors |
Q34808308 | Notch signalling is required for the formation of structurally stable muscle fibres in zebrafish |
Q37329964 | Replication of long-bone length QTL in the F9-F10 LG,SM advanced intercross. |
Q48230461 | Upstream regulation for initiation of restricted Shh expression in the chick limb bud. |
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