Literature DB >> 10508501

Incriminating gene suspects, Prader-Willi style.

R D Nicholls.   

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Year:  1999        PMID： 10508501     DOI： 10.1038/13758

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


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  13 in total

Review 1.  Imprinted expression of small nucleolar RNAs in brain: time for RNomics.

Authors:  W Filipowicz
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

Review 2.  The impact of genomic imprinting for neurobehavioral and developmental disorders.

Authors:  R D Nicholls
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

3.  Hypothalamic expression of snoRNA Snord116 is consistent with a link to the hyperphagia and obesity symptoms of Prader-Willi syndrome.

Authors:  Qian Zhang; Gerrit J Bouma; Kristy McClellan; Stuart Tobet
Journal:  Int J Dev Neurosci       Date:  2012-06-01       Impact factor: 2.457

4.  Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization.

Authors:  J Cavaillé; K Buiting; M Kiefmann; M Lalande; C I Brannan; B Horsthemke; J P Bachellerie; J Brosius; A Hüttenhofer
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

5.  Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome.

Authors:  Douglas C Bittel; Nataliya Kibiryeva; Steven G McNulty; Daniel J Driscoll; Merlin G Butler; Robert A White
Journal:  Am J Med Genet A       Date:  2007-03-01       Impact factor: 2.802

6.  Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

Authors:  Douglas C Bittel; Nataliya Kibiryeva; Susan M Sell; Theresa V Strong; Merlin G Butler
Journal:  Am J Med Genet A       Date:  2007-03-01       Impact factor: 2.802

7.  Deficits in social attribution ability in Prader-Willi syndrome.

Authors:  Kathleen Koenig; Ami Klin; Robert Schultz
Journal:  J Autism Dev Disord       Date:  2004-10

8.  Separate necdin domains bind ARNT2 and HIF1alpha and repress transcription.

Authors:  Eitan R Friedman; Chen-Ming Fan
Journal:  Biochem Biophys Res Commun       Date:  2007-08-29       Impact factor: 3.575

9.  Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.

Authors:  J-H Chai; D P Locke; J M Greally; J H M Knoll; T Ohta; J Dunai; A Yavor; E E Eichler; R D Nicholls
Journal:  Am J Hum Genet       Date:  2003-09-23       Impact factor: 11.025

10.  Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.

Authors:  D C Bittel; N Kibiryeva; Z Talebizadeh; M G Butler
Journal:  J Med Genet       Date:  2003-08       Impact factor: 6.318
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