NELL1
NELL1 (Neural EGFL like 1) هوَ بروتين يُشَفر بواسطة جين NELL1 في الإنسان.[1][2][3]
الوظيفة
المراجع
- "Entrez Gene: NELL1 NEL-like 1 (chicken)"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "Cloning and characterization of two novel human cDNAs (NELL1 and NELL2) encoding proteins with six EGF-like repeats"، Genomics، 38 (3): 273–6، مارس 1997، doi:10.1006/geno.1996.0628، PMID 8975702.
- "Study reveals bone-building protein's impact on bone stem cells"، مؤرشف من الأصل في 21 سبتمبر 2018.
قراءة متعمقة
- "[IMAGE: molecular integration of the analysis of the human genome and its expression]"، Comptes Rendus de l'Académie des Sciences, Série III، 318 (2): 263–72، 1995، PMID 7757816.
- "Human NELL-1 expressed in unilateral coronal synostosis."، J. Bone Miner. Res.، 14 (1): 80–9، 1999، doi:10.1359/jbmr.1999.14.1.80، PMID 9893069.
- "The neuronal EGF-related genes NELL1 and NELL2 are expressed in hemopoietic cells and developmentally regulated in the B lineage."، Gene، 231 (1–2): 121–6، 1999، doi:10.1016/S0378-1119(99)00093-1، PMID 10231576.
- "Biochemical characterization and expression analysis of neural thrombospondin-1-like proteins NELL1 and NELL2"، Biochem. Biophys. Res. Commun.، 265 (1): 79–86، 1999، doi:10.1006/bbrc.1999.1638، PMID 10548494.
- "Brain specific human genes, NELL1 and NELL2, are predominantly expressed in neuroblastoma and other embryonal neuroepithelial tumors"، Neurol. Med. Chir. (Tokyo)، 41 (12): 582–8, discussion 589، 2002، doi:10.2176/nmc.41.582، PMID 11803583.
- "Craniosynostosis in transgenic mice overexpressing Nell-1"، J. Clin. Invest.، 110 (6): 861–70، 2002، doi:10.1172/JCI15375، PMC 151127، PMID 12235118.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Identification of NAD+-dependent isocitrate dehydrogenase 3 gamma-like (IDH3GL) gene and its genetic polymorphisms"، Gene، 323: 141–8، 2004، doi:10.1016/j.gene.2003.09.014، PMID 14659887.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs"، Nat. Genet.، 36 (1): 40–5، 2004، doi:10.1038/ng1285، PMID 14702039.
- "The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD)"، Am. J. Hum. Genet.، 74 (6): 1255–61، 2004، doi:10.1086/421527، PMC 1182089، PMID 15124103.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration"، Cell، 125 (4): 801–14، 2006، doi:10.1016/j.cell.2006.03.032، PMID 16713569.
- "Craniosynostosis-associated gene nell-1 is regulated by runx2"، J. Bone Miner. Res.، 22 (1): 7–18، 2007، doi:10.1359/jbmr.061012، PMID 17042739.
- "Hypermethylation of the nel-like 1 gene is a common and early event and is associated with poor prognosis in early-stage esophageal adenocarcinoma"، Oncogene، 26 (43): 6332–40، 2007، doi:10.1038/sj.onc.1210461، PMID 17452981.
بوابة علم الأحياء الخلوي والجزيئي
بوابة طب
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