PubMed (GeneRIF) for id: 244329

Year	Number of Results
2010	3
2011	3
2013	1
2014	1
2015	1
2021	1
2022	1
2024	0

1

The Central Domain of MCPH1 Controls Development of the Cerebral Cortex and Gonads in Mice.

Wang Y, Zong W, Sun W, Chen C, Wang ZQ, Li T. Wang Y, et al. Cells. 2022 Aug 31;11(17):2715. doi: 10.3390/cells11172715. Cells. 2022. PMID: 36078123 Free PMC article.

2

The N-terminal BRCT domain determines MCPH1 function in brain development and fertility.

Liu X, Schneble-Löhnert N, Kristofova M, Qing X, Labisch J, Hofmann S, Ehrenberg S, Sannai M, Jörß T, Ori A, Godmann M, Wang ZQ. Liu X, et al. Cell Death Dis. 2021 Feb 1;12(2):143. doi: 10.1038/s41419-021-03406-3. Cell Death Dis. 2021. PMID: 33542216 Free PMC article.

3

Mcph1/Brit1 deficiency promotes genomic instability and tumor formation in a mouse model.

Liang Y, Gao H, Lin SY, Goss JA, Du C, Li K. Liang Y, et al. Oncogene. 2015 Aug 13;34(33):4368-78. doi: 10.1038/onc.2014.367. Epub 2014 Nov 3. Oncogene. 2015. PMID: 25362854 Free PMC article.

4

Mcph1-deficient mice reveal a role for MCPH1 in otitis media.

Chen J, Ingham N, Clare S, Raisen C, Vancollie VE, Ismail O, McIntyre RE, Tsang SH, Mahajan VB, Dougan G, Adams DJ, White JK, Steel KP. Chen J, et al. PLoS One. 2013;8(3):e58156. doi: 10.1371/journal.pone.0058156. Epub 2013 Mar 13. PLoS One. 2013. PMID: 23516444 Free PMC article.

5

MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway.

Gruber R, Zhou Z, Sukchev M, Joerss T, Frappart PO, Wang ZQ. Gruber R, et al. Nat Cell Biol. 2011 Sep 25;13(11):1325-34. doi: 10.1038/ncb2342. Nat Cell Biol. 2011. PMID: 21947081

6

VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling.

Passemard S, El Ghouzzi V, Nasser H, Verney C, Vodjdani G, Lacaud A, Lebon S, Laburthe M, Robberecht P, Nardelli J, Mani S, Verloes A, Gressens P, Lelièvre V. Passemard S, et al. J Clin Invest. 2011 Aug;121(8):3071-87. doi: 10.1172/JCI43824. J Clin Invest. 2011. PMID: 21737879 Free PMC article.

7

SET nuclear oncogene associates with microcephalin/MCPH1 and regulates chromosome condensation.

Leung JW, Leitch A, Wood JL, Shaw-Smith C, Metcalfe K, Bicknell LS, Jackson AP, Chen J. Leung JW, et al. J Biol Chem. 2011 Jun 17;286(24):21393-400. doi: 10.1074/jbc.M110.208793. Epub 2011 Apr 22. J Biol Chem. 2011. PMID: 21515671 Free PMC article.

8

Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function.

Trimborn M, Ghani M, Walther DJ, Dopatka M, Dutrannoy V, Busche A, Meyer F, Nowak S, Nowak J, Zabel C, Klose J, Esquitino V, Garshasbi M, Kuss AW, Ropers HH, Mueller S, Poehlmann C, Gavvovidis I, Schindler D, Sperling K, Neitzel H. Trimborn M, et al. PLoS One. 2010 Feb 16;5(2):e9242. doi: 10.1371/journal.pone.0009242. PLoS One. 2010. PMID: 20169082 Free PMC article.

9

BRIT1/MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability in mice.

Liang Y, Gao H, Lin SY, Peng G, Huang X, Zhang P, Goss JA, Brunicardi FC, Multani AS, Chang S, Li K. Liang Y, et al. PLoS Genet. 2010 Jan 22;6(1):e1000826. doi: 10.1371/journal.pgen.1000826. PLoS Genet. 2010. PMID: 20107607 Free PMC article.

10

Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1.

Farooq M, Baig S, Tommerup N, Kjaer KW. Farooq M, et al. Am J Med Genet A. 2010 Feb;152A(2):495-7. doi: 10.1002/ajmg.a.33234. Am J Med Genet A. 2010. PMID: 20101680 No abstract available.

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