Literature DB >> 15338008

Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation.

Inessa Grinberg1, Hope Northrup, Holly Ardinger, Chitra Prasad, William B Dobyns, Kathleen J Millen.   

Abstract

Dandy-Walker malformation (DWM; OMIM #220200) is a common but poorly understood congenital cerebellar malformation in humans. Through physical mapping of 3q2 interstitial deletions in several individuals with DWM, we defined the first critical region associated with DWM, encompassing two adjacent Zinc finger in cerebellum genes, ZIC1 and ZIC4. Mice with a heterozygous deletion of these two linked genes have a phenotype that closely resembles DWM, providing a mouse model for this malformation.

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Year:  2004        PMID: 15338008     DOI: 10.1038/ng1420

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  74 in total

1.  Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2.

Authors:  Melissa B Ramocki; Fernando Scaglia; Pawel Stankiewicz; John W Belmont; Jeremy Y Jones; Gary D Clark
Journal:  Am J Med Genet A       Date:  2011-06-02       Impact factor: 2.802

2.  CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592.

Authors:  Elsa Nicolas; Yannick Poitelon; Eliane Chouery; Nabiha Salem; Nicolas Levy; André Mégarbané; Valérie Delague
Journal:  Eur J Hum Genet       Date:  2010-06-09       Impact factor: 4.246

Review 3.  Novel approaches to studying the genetic basis of cerebellar development.

Authors:  Samin A Sajan; Kathryn E Waimey; Kathleen J Millen
Journal:  Cerebellum       Date:  2010-09       Impact factor: 3.847

4.  Bilateral perysilvian polymicrogyria in Chiari I malformation.

Authors:  Alberto Spalice; Pasquale Parisi; Mario Mastrangelo; Francesca De Luca; Alberto Verrotti; Paola Iannetti
Journal:  Childs Nerv Syst       Date:  2006-10-13       Impact factor: 1.475

5.  13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.

Authors:  Lucia Ballarati; Elena Rossi; Maria Teresa Bonati; Stefania Gimelli; Paola Maraschio; Palma Finelli; Sabrina Giglio; Elisabetta Lapi; Maria Francesca Bedeschi; Silvana Guerneri; Giulia Arrigo; Maria Grazia Patricelli; Teresa Mattina; Oriana Guzzardi; Vanna Pecile; Adalgisa Police; Gioacchino Scarano; Lidia Larizza; Orsetta Zuffardi; Daniela Giardino
Journal:  J Med Genet       Date:  2007-01       Impact factor: 6.318

Review 6.  Developmental biology of the meninges.

Authors:  Krishnakali Dasgupta; Juhee Jeong
Journal:  Genesis       Date:  2019-03-13       Impact factor: 2.487

7.  Differential gene expression in the developing lateral geniculate nucleus and medial geniculate nucleus reveals novel roles for Zic4 and Foxp2 in visual and auditory pathway development.

Authors:  Sam Horng; Gabriel Kreiman; Charlene Ellsworth; Damon Page; Marissa Blank; Kathleen Millen; Mriganka Sur
Journal:  J Neurosci       Date:  2009-10-28       Impact factor: 6.167

Review 8.  Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain.

Authors:  Kimberly A Aldinger; Gina E Elsen; Victoria E Prince; Kathleen J Millen
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

9.  Chromosomal map of human brain malformations.

Authors:  Nataliya Tyshchenko; Iosif Lurie; Albert Schinzel
Journal:  Hum Genet       Date:  2008-06-18       Impact factor: 4.132

10.  Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity.

Authors:  Ali Jalali; Kimberly A Aldinger; Ajit Chary; David G McLone; Robin M Bowman; Luan Cong Le; Phillip Jardine; Ruth Newbury-Ecob; Andrew Mallick; Nadereh Jafari; Eric J Russell; John Curran; Pam Nguyen; Karim Ouahchi; Charles Lee; William B Dobyns; Kathleen J Millen; Joao M Pina-Neto; John A Kessler; Alexander G Bassuk
Journal:  Hum Genet       Date:  2008-01-19       Impact factor: 4.132

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