Pages that link to "Q34439564"
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The following pages link to Craniosynostosis: genes and mechanisms (Q34439564):
Displaying 50 items.
- FGF-19, a novel fibroblast growth factor with unique specificity for FGFR4 (Q22010687) (← links)
- Cellular signaling by fibroblast growth factor receptors (Q24301087) (← links)
- Down-regulation of ubiquitin ligase Cbl induced by twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferation (Q24304940) (← links)
- Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutations (Q24310067) (← links)
- Identification of receptor and heparin binding sites in fibroblast growth factor 4 by structure-based mutagenesis (Q24550863) (← links)
- Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies (Q24675596) (← links)
- Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C (Q24681331) (← links)
- A Genetic-Pathophysiological Framework for Craniosynostosis (Q26784240) (← links)
- Metopic synostosis (Q26823808) (← links)
- Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome (Q28142988) (← links)
- Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes (Q28212192) (← links)
- Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays (Q28294932) (← links)
- TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome (Q28296558) (← links)
- Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis (Q28344714) (← links)
- Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome (Q28509010) (← links)
- FGF18 is required for normal cell proliferation and differentiation during osteogenesis and chondrogenesis (Q28586991) (← links)
- Gli3Xt-J/Xt-J mice exhibit lambdoid suture craniosynostosis which results from altered osteoprogenitor proliferation and differentiation (Q28587566) (← links)
- FGF9 regulates early hypertrophic chondrocyte differentiation and skeletal vascularization in the developing stylopod (Q28592971) (← links)
- Sox2 induction by FGF and FGFR2 activating mutations inhibits Wnt signaling and osteoblast differentiation (Q28593870) (← links)
- Derivation of the mammalian skull vault (Q28767309) (← links)
- Evidence for digenic inheritance in some cases of Antley-Bixler syndrome? (Q30443021) (← links)
- Presphenoidal synchondrosis fusion in DBA/2J mice (Q30458724) (← links)
- Hedgehog-dependent proliferation drives modular growth during morphogenesis of a dermal bone (Q30514571) (← links)
- Psychiatric genetics: a genetic basis for health? (Q33636282) (← links)
- Mutations in the human TWIST gene (Q33825444) (← links)
- The impact of molecular genetics on oral health paradigms (Q33842939) (← links)
- Adipose-derived stem cells: a review of signaling networks governing cell fate and regenerative potential in the context of craniofacial and long bone skeletal repair (Q33907462) (← links)
- Distinct Caenorhabditis elegans HLH-8/twist-containing dimers function in the mesoderm (Q33915482) (← links)
- Fibroblast growth factor signaling and basement membrane assembly are connected during epithelial morphogenesis of the embryoid body (Q33946703) (← links)
- Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature. (Q33947191) (← links)
- The balance of WNT and FGF signaling influences mesenchymal stem cell fate during skeletal development (Q33987011) (← links)
- Mutations in fam20b and xylt1 Reveal That Cartilage Matrix Controls Timing of Endochondral Ossification by Inhibiting Chondrocyte Maturation (Q34013662) (← links)
- Kinase mutations in human disease: interpreting genotype-phenotype relationships (Q34088851) (← links)
- Characterization of distinct classes of differential gene expression in osteoblast cultures from non-syndromic craniosynostosis bone (Q34112919) (← links)
- C. elegans twist gene expression in differentiated cell types is controlled by autoregulation through intron elements (Q34154831) (← links)
- The BMP antagonist noggin regulates cranial suture fusion (Q34189687) (← links)
- Management of Craniosynostosis (Q34192513) (← links)
- The BMP ligand Gdf6 prevents differentiation of coronal suture mesenchyme in early cranial development (Q34302263) (← links)
- Phenotypic findings due to trisomy 7p15.3-pter including the TWIST locus (Q34373526) (← links)
- The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect (Q34380582) (← links)
- A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. (Q34387671) (← links)
- De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome (Q34388821) (← links)
- Regulation of mandibular growth and morphogenesis (Q34402686) (← links)
- Cranial suture biology (Q34407265) (← links)
- A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22. (Q34439719) (← links)
- Molecular-pathogenetic classification of genetic disorders of the skeleton (Q34561450) (← links)
- A biochemist's guide to Caenorhabditis elegans (Q34570449) (← links)
- Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen Syndrome (Q34575381) (← links)
- A new method for generating point mutations in bacterial artificial chromosomes by homologous recombination in Escherichia coli (Q34584758) (← links)
- A case report of a patient with Pfeiffer syndrome, an FGRF 2 mutation (Trp290Cys) and unique ocular anterior segment findings (Q34623067) (← links)