Literature DB >> 19459880

An X-linked microcephaly syndrome caused by disruptions of CASK implicates the CASK-TBR1-RELN pathway in human brain development.

Kathleen A Bailey1, Kimbery A Aldinger.   

Abstract

Entities:  

Year:  2009        PMID： 19459880     DOI： 10.1111/j.1399-0004.2009.01186_1.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

1.  The molecular basis of the Caskin1 and Mint1 interaction with CASK.

Authors:  Ryan L Stafford; Jason Ear; Mary Jane Knight; James U Bowie
Journal:  J Mol Biol       Date:  2011-07-12       Impact factor: 5.469

2.  Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders.

Authors:  Ling Zhang; Jingmin Wang; Cheng Zhang; Dongxiao Li; Claudia M B Carvalho; Haoran Ji; Jianqiu Xiao; Ye Wu; Weichen Zhou; Hongyan Wang; Li Jin; Yang Luo; Xiru Wu; James R Lupski; Feng Zhang; Yuwu Jiang
Journal:  Hum Mol Genet       Date:  2017-05-15       Impact factor: 6.150

Review 3.  The Non-Linear Path from Gene Dysfunction to Genetic Disease: Lessons from the MICPCH Mouse Model.

Authors:  Konark Mukherjee; Leslie E W LaConte; Sarika Srivastava
Journal:  Cells       Date:  2022-03-28       Impact factor: 6.600
  3 in total

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