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Microcephaly.

作者信息

Woods C G, Basto R

机构信息

Cambridge Institute for Medical Research, Cambridge University, Addenbrookes Hospital, Cambridge, UK.

UMR144, CNRS, Institute Curie, Paris, France.

出版信息

Curr Biol. 2014 Dec 1;24(23):R1109-11. doi: 10.1016/j.cub.2014.09.063.

DOI:10.1016/j.cub.2014.09.063

PMID:25465325

Abstract

摘要

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相似文献

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Am J Med Genet A. 2010 Feb;152A(2):495-7. doi: 10.1002/ajmg.a.33234.

Brain evolution: microcephaly genes weigh in.

Curr Biol. 2010 Mar 9;20(5):R244-6. doi: 10.1016/j.cub.2010.01.043.

Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency.

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J Evol Biol. 2013 Apr;26(4):906-11. doi: 10.1111/jeb.12091. Epub 2013 Jan 11.

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Curr Opin Cell Biol. 2006 Feb;18(1):95-101. doi: 10.1016/j.ceb.2005.11.004. Epub 2005 Dec 6.

Autosomal recessive primary microcephalies (MCPH).

Eur J Paediatr Neurol. 2014 Jul;18(4):547-8. doi: 10.1016/j.ejpn.2014.03.010. Epub 2014 Apr 16.

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Nat Genet. 2010 Nov;42(11):923-4. doi: 10.1038/ng1110-923.

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FEBS Lett. 2014 Aug 1;588(15):2366-72. doi: 10.1016/j.febslet.2014.06.030. Epub 2014 Jun 18.

Evolution. Are human brains still evolving? Brain genes show signs of selection.

Science. 2005 Sep 9;309(5741):1662-3. doi: 10.1126/science.309.5741.1662.

引用本文的文献

Cytoplasmic control of spindle architecture.

Nat Cell Biol. 2025 Jun;27(6):884-885. doi: 10.1038/s41556-025-01686-x.

Cell state-specific cytoplasmic density controls spindle architecture and scaling.

Nat Cell Biol. 2025 Jun;27(6):959-971. doi: 10.1038/s41556-025-01678-x. Epub 2025 Jun 13.

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Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.

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J Cell Biol. 2021 Aug 2;220(8). doi: 10.1083/jcb.202007171. Epub 2021 Jun 17.

PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly.

Clin Genet. 2020 Jul;98(1):80-85. doi: 10.1111/cge.13756. Epub 2020 May 17.

MCPH1 Lack of Function Enhances Mitotic Cell Sensitivity Caused by Catalytic Inhibitors of Topo II.

Genes (Basel). 2020 Apr 8;11(4):406. doi: 10.3390/genes11040406.

Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathways.

Hum Mutat. 2020 Feb;41(2):512-524. doi: 10.1002/humu.23948. Epub 2019 Nov 27.

MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis.

PLoS Biol. 2018 Dec 19;16(12):e2006613. doi: 10.1371/journal.pbio.2006613. eCollection 2018 Dec.

MCPH1, mutated in primary microcephaly, is required for efficient chromosome alignment during mitosis.

Sci Rep. 2017 Oct 12;7(1):13019. doi: 10.1038/s41598-017-12793-7.