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 2010-12-05.
- Watanabe TK، Katagiri T، Suzuki M، Shimizu F، Fujiwara T، Kanemoto N، Nakamura Y، Hirai Y، Maekawa H، Takahashi E (مارس 1997). "Cloning and characterization of two novel human cDNAs (NELL1 and NELL2) encoding proteins with six EGF-like repeats". Genomics. ج. 38 ع. 3: 273–6. DOI:10.1006/geno.1996.0628. PMID:8975702.
- "Study reveals bone-building protein's impact on bone stem cells". مؤرشف من الأصل في 2018-09-21.
قراءة متعمقة
- Auffray C، Behar G، Bois F، وآخرون (1995). "[IMAGE: molecular integration of the analysis of the human genome and its expression]". Comptes Rendus de l'Académie des Sciences, Série III. ج. 318 ع. 2: 263–72. PMID:7757816.
- Ting K، Vastardis H، Mulliken JB، وآخرون (1999). "Human NELL-1 expressed in unilateral coronal synostosis". J. Bone Miner. Res. ج. 14 ع. 1: 80–9. DOI:10.1359/jbmr.1999.14.1.80. PMID:9893069.
- Luce MJ، Burrows PD (1999). "The neuronal EGF-related genes NELL1 and NELL2 are expressed in hemopoietic cells and developmentally regulated in the B lineage". Gene. ج. 231 ع. 1–2: 121–6. DOI:10.1016/S0378-1119(99)00093-1. PMID:10231576.
- Kuroda S، Oyasu M، Kawakami M، وآخرون (1999). "Biochemical characterization and expression analysis of neural thrombospondin-1-like proteins NELL1 and NELL2". Biochem. Biophys. Res. Commun. ج. 265 ع. 1: 79–86. DOI:10.1006/bbrc.1999.1638. PMID:10548494.
- Maeda K، Matsuhashi S، Tabuchi K، وآخرون (2002). "Brain specific human genes, NELL1 and NELL2, are predominantly expressed in neuroblastoma and other embryonal neuroepithelial tumors". Neurol. Med. Chir. (Tokyo). ج. 41 ع. 12: 582–8, discussion 589. DOI:10.2176/nmc.41.582. PMID:11803583.
- Zhang X، Kuroda S، Carpenter D، وآخرون (2002). "Craniosynostosis in transgenic mice overexpressing Nell-1". J. Clin. Invest. ج. 110 ع. 6: 861–70. DOI:10.1172/JCI15375. PMC:151127. PMID:12235118.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Okamoto K، Matsuzaka Y، Yoshikawa Y، وآخرون (2004). "Identification of NAD+-dependent isocitrate dehydrogenase 3 gamma-like (IDH3GL) gene and its genetic polymorphisms". Gene. ج. 323: 141–8. DOI:10.1016/j.gene.2003.09.014. PMID:14659887.
- Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
- Tsutsumi S، Kamata N، Vokes TJ، وآخرون (2004). "The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD)". Am. J. Hum. Genet. ج. 74 ع. 6: 1255–61. DOI:10.1086/421527. PMC:1182089. PMID:15124103.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
- Lim J، Hao T، Shaw C، وآخرون (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration". Cell. ج. 125 ع. 4: 801–14. DOI:10.1016/j.cell.2006.03.032. PMID:16713569.
- Truong T، Zhang X، Pathmanathan D، وآخرون (2007). "Craniosynostosis-associated gene nell-1 is regulated by runx2". J. Bone Miner. Res. ج. 22 ع. 1: 7–18. DOI:10.1359/jbmr.061012. PMID:17042739.
- Jin Z، Mori Y، Yang J، وآخرون (2007). "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. ج. 26 ع. 43: 6332–40. DOI:10.1038/sj.onc.1210461. PMID:17452981.
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