Radiation-induced delayed cell death in a hypomorphic Artemis cell line

By Evans Paul M.   Woodbine Lisa   Riballo Enriquetta   Gennery Andrew R.   Hubank Michael  

Human Molecular Genetics, Vol. 15, Iss. 8, 2006-04 ,pp. : 1303-1311

Oxford University Press

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A hypomorphic allele of Tsc2 highlights the role of TSC1/TSC2 in signaling to AKT and models mild human TSC2 alleles

By Pollizzi Kristen   Malinowska-Kolodziej Izabela   Doughty Cheryl   Betz Charles   Ma Jian   Goto June   Kwiatkowski David J.  

Human Molecular Genetics, Vol. 18, Iss. 13, 2009-07 ,pp. : 2378-2387

Oxford University Press

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The relationship between somatic mtDNA rearrangements, human heart disease and aging

By Kajander O.A.  

Human Molecular Genetics, Vol. 11, Iss. 3, 2002-02 ,pp. : 317-324

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An MYH9 human disease model in flies: site-directed mutagenesis of the Drosophila non-muscle myosin II results in hypomorphic alleles with dominant character

By Franke Josef D.   Montague Ruth A.   Rickoll Wayne L.   Kiehart Daniel P.  

Human Molecular Genetics, Vol. 16, Iss. 24, 2007-12 ,pp. : 3160-3173

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Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer’s disease by increased A β 42 secretion

By Jonghe Chris De   Cruts Marc   Rogaeva Ekaterina A.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1529-1540

Oxford University Press

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