Pages that link to "Q46697162"
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The following pages link to A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia (Q46697162):
Displaying 50 items.
- Connexins: a myriad of functions extending beyond assembly of gap junction channels (Q21245510) (← links)
- Life cycle of connexins in health and disease (Q24541428) (← links)
- Bidirectional communication between oocytes and follicle cells: ensuring oocyte developmental competence (Q24634160) (← links)
- Gap junctions couple astrocytes and oligodendrocytes (Q24645936) (← links)
- Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (Q26801599) (← links)
- Gap junctions in inherited human disorders of the central nervous system (Q26823332) (← links)
- Gap junctional regulation of signal transduction in bone cells (Q26824408) (← links)
- Gap junction connexins in female reproductive organs: implications for women's reproductive health (Q27002892) (← links)
- Ultrasound biomicroscopy in small animal research: applications in molecular and preclinical imaging. (Q27025201) (← links)
- A nonsense mutation in the first transmembrane domain of connexin 43 underlies autosomal recessive oculodentodigital syndrome (Q28249865) (← links)
- Interaction of connexin43 and protein kinase C-delta during FGF2 signaling (Q28506823) (← links)
- Caveolin-1 and -2 interact with connexin43 and regulate gap junctional intercellular communication in keratinocytes (Q28574327) (← links)
- Osteoblast connexin43 modulates skeletal architecture by regulating both arms of bone remodeling (Q28592164) (← links)
- If the skull fits: magnetic resonance imaging and microcomputed tomography for combined analysis of brain and skull phenotypes in the mouse (Q28717198) (← links)
- Premature osteoblast clustering by enamel matrix proteins induces osteoblast differentiation through up-regulation of connexin 43 and N-cadherin (Q28741433) (← links)
- Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia (Q30419343) (← links)
- Inhibition of gap junction communication at ectopic Eph/ephrin boundaries underlies craniofrontonasal syndrome (Q33257263) (← links)
- Bone marrow connexin-43 expression is critical for hematopoietic regeneration after chemotherapy (Q33370523) (← links)
- Cytopenia induction by 5-fluorouracil identifies thrombopoietic mutants in sensitized ENU mutagenesis screens (Q33397260) (← links)
- The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans. (Q33762572) (← links)
- A dominant loss-of-function GJA1 (Cx43) mutant impairs parturition in the mouse (Q33770586) (← links)
- Depression of intraocular pressure following inactivation of connexin43 in the nonpigmented epithelium of the ciliary body (Q33831809) (← links)
- Transcription factor FoxO1 is essential for enamel biomineralization (Q34146020) (← links)
- Connexin mutant embryonic stem cells and human diseases (Q34259105) (← links)
- Characterization of hTERT-immortalized osteoblast cell lines generated from wild-type and connexin43-null mouse calvaria (Q34304843) (← links)
- Syndromic and non-syndromic disease-linked Cx43 mutations (Q34398416) (← links)
- First mouse model for combined osteogenesis imperfecta and Ehlers-Danlos syndrome (Q34398977) (← links)
- Mutations in cardiovascular connexin genes (Q34426537) (← links)
- Gap junction intercellular communication: a review of a potential platform to modulate craniofacial tissue engineering (Q34778768) (← links)
- Connexin 43 as a signaling platform for increasing the volume and spatial distribution of regenerated tissue (Q34993780) (← links)
- Connexin 43 channels are essential for normal bone structure and osteocyte viability (Q35096932) (← links)
- Up-regulation of BMP2/4 signaling increases both osteoblast-specific marker expression and bone marrow adipogenesis in Gja1Jrt/+ stromal cell cultures (Q35125177) (← links)
- The transcriptional activity of osterix requires the recruitment of Sp1 to the osteocalcin proximal promoter (Q35205544) (← links)
- Human dermal fibroblasts derived from oculodentodigital dysplasia patients suggest that patients may have wound-healing defects (Q35234343) (← links)
- Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse models (Q35573969) (← links)
- Connexin43 phosphorylation in brain, cardiac, endothelial and epithelial tissues (Q35621893) (← links)
- Myogenic bladder defects in mouse models of human oculodentodigital dysplasia (Q35687852) (← links)
- Advances in the Molecular Genetics of Non-syndromic Syndactyly. (Q35697709) (← links)
- Connexin43 deficiency reduces the sensitivity of cortical bone to the effects of muscle paralysis (Q35835319) (← links)
- Connexins and pannexins in the skeleton: gap junctions, hemichannels and more (Q35855335) (← links)
- ERK acts in parallel to PKCδ to mediate the connexin43-dependent potentiation of Runx2 activity by FGF2 in MC3T3 osteoblasts (Q35900708) (← links)
- Cx43-Dependent Skeletal Phenotypes Are Mediated by Interactions between the Hapln1a-ECM and Sema3d during Fin Regeneration (Q35909574) (← links)
- CONNEXIN 43 AND BONE: NOT JUST A GAP JUNCTION PROTEIN. (Q36008760) (← links)
- Role of connexins and pannexins during ontogeny, regeneration, and pathologies of bone (Q36031679) (← links)
- Biological role of connexin intercellular channels and hemichannels (Q36035603) (← links)
- Connexin-43 prevents hematopoietic stem cell senescence through transfer of reactive oxygen species to bone marrow stromal cells (Q36061498) (← links)
- A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis (Q36115086) (← links)
- Gap junctions and hemichannels in signal transmission, function and development of bone (Q36231023) (← links)
- Impact of obesity on 7,12-dimethylbenz[a]anthracene-induced altered ovarian connexin gap junction proteins in female mice (Q36271288) (← links)
- Gap junction remodeling and cardiac arrhythmogenesis in a murine model of oculodentodigital dysplasia. (Q36300072) (← links)