Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a

By Meng Linyan   Person Richard E.   Beaudet Arthur L.  

Human Molecular Genetics, Vol. 21, Iss. 13, 2012-07 ,pp. : 3001-3012

Oxford University Press

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DAPK1 variants are associated with Alzheimer's disease and allele-specific expression

By Li Yonghong   Grupe Andrew   Rowland Charles   Nowotny Petra   Kauwe John S.K.   Smemo Scott   Hinrichs Anthony   Tacey Kristina   Toombs Timothy A.   Kwok Shirley   Catanese Joseph   White Thomas J.   Maxwell Taylor J.   Hollingworth Paul   Abraham Richard   Rubinsztein David C.   Brayne Carol   Wavrant-De Vrièze Fabienne   Hardy John   O'Donovan Michael   Lovestone Simon   Morris John C.   Thal Leon J.   Owen Michael   Williams Julie   Goate Alison  

Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2560-2568

Oxford University Press

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Identification and characterization of MTR1 , a novel gene with homology to melastatin ( MLSN1 ) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

By Prawitt Dirk   Enklaar Thorsten   Klemm Gabi   Gärtner Barbara   Spangenberg Christian   Winterpacht Andreas   Higgins Michael  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 203-216

Oxford University Press

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Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression

By Korade-Mirnics Zeljka   Tarleton Jack  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1017-1023

Oxford University Press

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Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2664-2673

John Wiley & Sons Inc

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