Literature DB >> 25465325

Microcephaly.

C G Woods1, R Basto2.   

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Year:  2014        PMID： 25465325     DOI： 10.1016/j.cub.2014.09.063

Source DB:  PubMed          Journal:  Curr Biol        ISSN： 0960-9822            Impact factor:   10.834


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  11 in total

Review 1.  Centrosomes in spindle organization and chromosome segregation: a mechanistic view.

Authors:  Patrick Meraldi
Journal:  Chromosome Res       Date:  2016-01       Impact factor: 5.239

2.  Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly.

Authors:  Hongda Li; Stephanie L Bielas; Maha S Zaki; Samira Ismail; Dorit Farfara; Kyongmi Um; Rasim O Rosti; Eric C Scott; Shu Tu; Neil C Chi; Stacey Gabriel; Emine Z Erson-Omay; A Gulhan Ercan-Sencicek; Katsuhito Yasuno; Ahmet Okay Çağlayan; Hande Kaymakçalan; Barış Ekici; Kaya Bilguvar; Murat Gunel; Joseph G Gleeson
Journal:  Am J Hum Genet       Date:  2016-07-21       Impact factor: 11.025

3.  Severe congenital microcephaly with AP4M1 mutation, a case report.

Authors:  Sarah Duerinckx; Helene Verhelst; Camille Perazzolo; Philippe David; Laurence Desmyter; Isabelle Pirson; Marc Abramowicz
Journal:  BMC Med Genet       Date:  2017-05-02       Impact factor: 2.103

4.  MEKK3 coordinates with FBW7 to regulate WDR62 stability and neurogenesis.

Authors:  Dan Xu; Minghui Yao; Yaqing Wang; Ling Yuan; Joerg D Hoeck; Jingwen Yu; Liang Liu; Yvonne Y C Yeap; Weiya Zhang; Feng Zhang; Yinghang Feng; Tiantian Ma; Yujie Wang; Dominic C H Ng; Xiaoyin Niu; Bing Su; Axel Behrens; Zhiheng Xu
Journal:  PLoS Biol       Date:  2018-12-19       Impact factor: 8.029

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

Authors:  María Arroyo; Antonio Sánchez; Ana Cañuelo; Rosalía F Heredia-Molina; Eduardo Martínez-Molina; Duncan J Clarke; Juan Alberto Marchal
Journal:  Genes (Basel)       Date:  2020-04-08       Impact factor: 4.096

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

Authors:  Sarah Duerinckx; Valérie Jacquemin; Séverine Drunat; Yoann Vial; Sandrine Passemard; Camille Perazzolo; Annick Massart; Julie Soblet; Judith Racapé; Laurence Desmyter; Cindy Badoer; Sofia Papadimitriou; Yann-Aël Le Borgne; Anne Lefort; Frédérick Libert; Viviane De Maertelaer; Marianne Rooman; Sabine Costagliola; Alain Verloes; Tom Lenaerts; Isabelle Pirson; Marc Abramowicz
Journal:  Hum Mutat       Date:  2019-11-27       Impact factor: 4.878

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

Authors:  Amjad Khan; Manal Alaamery; Salam Massadeh; Abdulrahman Obaid; Amna A Kashgari; Christopher A Walsh; Wafaa Eyaid
Journal:  Clin Genet       Date:  2020-05-17       Impact factor: 4.438

8.  WDR62 localizes katanin at spindle poles to ensure synchronous chromosome segregation.

Authors:  Amanda Guerreiro; Filipe De Sousa; Nicolas Liaudet; Daria Ivanova; Anja Eskat; Patrick Meraldi
Journal:  J Cell Biol       Date:  2021-06-17       Impact factor: 10.539

9.  Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities.

Authors:  Mohan Narayanan; Keri Ramsey; Theresa Grebe; Isabelle Schrauwen; Szabolcs Szelinger; Matthew Huentelman; David Craig; Vinodh Narayanan
Journal:  F1000Res       Date:  2015-09-28

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

Authors:  M Arroyo; R Kuriyama; M Trimborn; D Keifenheim; A Cañuelo; A Sánchez; D J Clarke; J A Marchal
Journal:  Sci Rep       Date:  2017-10-12       Impact factor: 4.379
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