Literature DB >> 11242098

Deconstructing DiGeorge syndrome.

M Schinke, S Izumo.   

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Year:  2001        PMID： 11242098     DOI： 10.1038/85784

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


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  10 in total

1.  Associations between human disease genes and overlapping gene groups and multiple amino acid runs.

Authors:  Samuel Karlin; Chingfer Chen; Andrew J Gentles; Michael Cleary
Journal:  Proc Natl Acad Sci U S A       Date:  2002-12-09       Impact factor: 11.205

2.  Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.

Authors:  Anne M Moon; Deborah L Guris; Ji-heui Seo; Leiming Li; Jennetta Hammond; Amy Talbot; Akira Imamoto
Journal:  Dev Cell       Date:  2006-01       Impact factor: 12.270

3.  A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.

Authors:  Fei Long; Xike Wang; Shaohai Fang; Yuejuan Xu; Kun Sun; Sun Chen; Rang Xu
Journal:  PLoS One       Date:  2013-08-29       Impact factor: 3.240

Review 4.  Immunological aspects of 22q11.2 deletion syndrome.

Authors:  A R Gennery
Journal:  Cell Mol Life Sci       Date:  2011-10-09       Impact factor: 9.261

5.  Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome.

Authors:  P Eberle; C Berger; S Junge; S Dougoud; E Valsangiacomo Büchel; M Riegel; A Schinzel; R Seger; T Güngör
Journal:  Clin Exp Immunol       Date:  2008-11-24       Impact factor: 4.330

6.  Developmental expression of the amphioxus Tbx1/ 10 gene illuminates the evolution of vertebrate branchial arches and sclerotome.

Authors:  Navin R Mahadevan; Amy C Horton; Jeremy J Gibson-Brown
Journal:  Dev Genes Evol       Date:  2004-09-11       Impact factor: 0.900

7.  Postmaturity in a genetic subtype of schizophrenia.

Authors:  E W C Chow; J Husted; R Weksberg; A S Bassett
Journal:  Acta Psychiatr Scand       Date:  2003-10       Impact factor: 6.392

8.  Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Authors:  Yue-Juan Xu; Jian Wang; Rang Xu; Peng-Jun Zhao; Xi-Ke Wang; Heng-Juan Sun; Li-Ming Bao; Jie Shen; Qi-Hua Fu; Fen Li; Kun Sun
Journal:  BMC Med Genet       Date:  2011-12-21       Impact factor: 2.103

Review 9.  The POZ/BTB and AT-Hook Containing Zinc Finger 1 (PATZ1) Transcription Regulator: Physiological Functions and Disease Involvement.

Authors:  Monica Fedele; Elvira Crescenzi; Laura Cerchia
Journal:  Int J Mol Sci       Date:  2017-11-24       Impact factor: 5.923

10.  Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome.

Authors:  Chen Yang; Cheng-Hung Huang; Mei-Leng Cheong; Kun-Long Hung; Lung-Huang Lin; Yeong-Seng Yu; Chih-Cheng Chien; Huei-Chen Huang; Chan-Wei Chen; Chi-Jung Huang
Journal:  BMC Med Genet       Date:  2009-02-25       Impact factor: 2.103
  10 in total

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