GDF5
GDF5 (Growth differentiation factor 5) هوَ بروتين يُشَفر بواسطة جين GDF5 في الإنسان.[1][2][3][3][4][5][6][7][8]
المراجع
- "Growth/differentiation factor-5 (GDF-5) and skeletal development"، J Bone Joint Surg Am، 83-A Suppl 1 (Pt 1): S23–30، 2001، PMID 11263662.
- "Mutations in CDMP1 cause autosomal dominant brachydactyly type C"، Nat Genet، 17 (1): 18–9، أكتوبر 1997، doi:10.1038/ng0997-18، PMID 9288091.
- "Entrez Gene: GDF5 growth differentiation factor 5 (cartilage-derived morphogenetic protein-1)"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Effects of growth/differentiation factor 5 on the survival and morphology of embryonic rat midbrain dopaminergic neurones in vitro"، J Neurocytol، 33 (5): 479–88، 2004، doi:10.1007/s11068-004-0511-y، PMID 15906156.
- "The role of growth/differentiation factor 5 (GDF5) in the induction and survival of midbrain dopaminergic neurones: relevance to Parkinson's disease treatment"، J Anat، 207 (3): 219–26، 2005، doi:10.1111/j.1469-7580.2005.00447.x، PMC 1571542، PMID 16185246.
- "BMP/GDF-signalling interactions during synovial joint development"، Cell Tissue Res، 296 (1): 111–9، 1999، doi:10.1007/s004410051272، PMID 10199971.
- "Mechanisms of GDF-5 action during skeletal development"، Development، 126 (6): 1305–15، 1999، PMID 10021348.
- "Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1"، Nat Genet، 17 (1): 58–64، أكتوبر 1997، doi:10.1038/ng0997-58، PMID 9288098.
قراءة متعمقة
- Reddi AH (1997)، "Cartilage morphogenesis: role of bone and cartilage morphogenetic proteins, homeobox genes and extracellular matrix"، Matrix Biol.، 14 (8): 599–606، doi:10.1016/S0945-053X(05)80024-1، PMID 9057810.
- Luyten FP (1998)، "Cartilage-derived morphogenetic protein-1"، Int. J. Biochem. Cell Biol.، 29 (11): 1241–4، doi:10.1016/S1357-2725(97)00025-3، PMID 9451821.
- "The family of bone morphogenetic proteins"، Kidney Int.، 57 (6): 2207–14، 2000، doi:10.1046/j.1523-1755.2000.00081.x، PMID 10844590.
- "Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia"، American Journal of Medical Genetics، 111 (1): 31–7، 2003، doi:10.1002/ajmg.10501، PMID 12124730.
- "Cartilage-derived morphogenetic proteins. New members of the transforming growth factor-beta superfamily predominantly expressed in long bones during human embryonic development"، J. Biol. Chem.، 269 (45): 28227–34، 1994، PMID 7961761.
- "Cloning and expression of recombinant human growth/differentiation factor 5"، Biochem. Biophys. Res. Commun.، 204 (2): 646–52، 1994، doi:10.1006/bbrc.1994.2508، PMID 7980526.
- "A human chondrodysplasia due to a mutation in a TGF-beta superfamily member"، Nat. Genet.، 12 (3): 315–7، 1996، doi:10.1038/ng0396-315، PMID 8589725.
- "Assignment of a new TGF-beta superfamily member, human cartilage-derived morphogenetic protein-1, to chromosome 20q11.2"، Genomics، 34 (1): 150–1، 1996، doi:10.1006/geno.1996.0257، PMID 8661040.
- "Identification of type I and type II serine/threonine kinase receptors for growth/differentiation factor-5"، J. Biol. Chem.، 271 (35): 21345–52، 1996، doi:10.1074/jbc.271.35.21345، PMID 8702914.
- "Cartilage-derived morphogenetic proteins and osteogenic protein-1 differentially regulate osteogenesis"، J. Bone Miner. Res.، 13 (3): 383–92، 1998، doi:10.1359/jbmr.1998.13.3.383، PMID 9525338.
- "Minimal promoter components of the human growth/differentiation factor-5 gene"، Biochem. Biophys. Res. Commun.، 263 (3): 707–13، 1999، doi:10.1006/bbrc.1999.1445، PMID 10512744.
- "Synergistic effects of different bone morphogenetic protein type I receptors on alkaline phosphatase induction"، J. Cell Sci.، 114 (Pt 8): 1483–9، 2001، PMID 11282024.
- "The DNA sequence and comparative analysis of human chromosome 20"، Nature، 414 (6866): 865–71، 2002، doi:10.1038/414865a، PMID 11780052.
- "Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)"، Clin. Genet.، 61 (6): 454–8، 2003، doi:10.1034/j.1399-0004.2002.610610.x، PMID 12121354.
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