Symbol Name ID |
Nbn
nibrin MGI:1351625 |
Age | E7 | E9.5 | E10.5 | E11 | E12.5 | E14.5 | E15 | E15.5 | E17 | E17.5 | E18.5 | E | P |
In situ RNA (section) | 1 | 1 | 1 | 1 | 1 | 1 | 1 | ||||||
In situ RNA (whole mount) | 1 | 1 | |||||||||||
Northern blot | 1 | 1 | 1 | 1 | 2 | ||||||||
Western blot | 1 | 1 | 2 | 1 | 1 | ||||||||
RT-PCR | 1 | 2 | |||||||||||
cDNA clones | 1 |
Nbn nibrin (Synonyms: Nbs1) | |
Results | Reference |
1 | J:306148 Chen Y, Sun J, Ju Z, Wang ZQ, Li T, Nbs1-mediated DNA damage repair pathway regulates haematopoietic stem cell development and embryonic haematopoiesis. Cell Prolif. 2021 Mar;54(3):e12972 |
2* | J:66992 Douglas KR, Camper SA, Partial transcriptome of the developing pituitary gland. Genomics. 2000 Dec 15;70(3):335-46 |
1* | J:91257 Gray PA, Fu H, Luo P, Zhao Q, Yu J, Ferrari A, Tenzen T, Yuk DI, Tsung EF, Cai Z, Alberta JA, Cheng LP, Liu Y, Stenman JM, Valerius MT, Billings N, Kim HA, Greenberg ME, McMahon AP, Rowitch DH, Stiles CD, Ma Q, Mouse Brain Organization Revealed Through Direct Genome-Scale TF Expression Analysis. Science. 2004 Dec 24;306(5705):2255-2257 |
1* | J:171409 GUDMAP Consortium, GUDMAP: the GenitoUrinary Development Molecular Anatomy Project. www.gudmap.org. 2004; |
1 | J:191367 Lee Y, Katyal S, Downing SM, Zhao J, Russell HR, McKinnon PJ, Neurogenesis requires TopBP1 to prevent catastrophic replicative DNA damage in early progenitors. Nat Neurosci. 2012 Jun;15(6):819-26 |
1 | J:181920 Lee Y, Shull ER, Frappart PO, Katyal S, Enriquez-Rios V, Zhao J, Russell HR, Brown EJ, McKinnon PJ, ATR maintains select progenitors during nervous system development. EMBO J. 2012 Mar 7;31(5):1177-89 |
3* | J:316150 Li R, Yang YG, Gao Y, Wang ZQ, Tong WM, A distinct response to endogenous DNA damage in the development of Nbs1-deficient cortical neurons. Cell Res. 2012 May;22(5):859-72 |
2 | J:204946 Rodrigues PM, Grigaravicius P, Remus M, Cavalheiro GR, Gomes AL, Martins MR, Frappart L, Reuss D, McKinnon PJ, von Deimling A, Martins RA, Frappart PO, Nbn and atm cooperate in a tissue and developmental stage-specific manner to prevent double strand breaks and apoptosis in developing brain and eye. PLoS One. 2013;8(7):e69209 |
5* | J:59119 Vissinga CS, Yeo TC, Woessner J, Massa HF, Wilson RK, Trask BJ, Concannon P, Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome. Cytogenet Cell Genet. 1999;87(1-2):80-4 |
8* | J:63741 Wilda M, Demuth I, Concannon P, Sperling K, Hameister H, Expression pattern of the nijmegen breakage syndrome gene, nbs1, during murine development. Hum Mol Genet. 2000 Jul 22;9(12):1739-44 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/12/2024 MGI 6.24 |
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