Mismatch repair (MMR) efficiency and MSH2 gene mutation in human colorectal carcinoma cell line COLO320HSR

By Tronov V.   Kramarenko I.   Zakharov S.  

Russian Journal of Genetics, Vol. 43, Iss. 4, 2007-04 ,pp. : 430-436

MAIK Nauka/Interperiodica

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Dominant phenotypes produced by the HD mutation in ST Hdh Q111 striatal cells

By Trettel Flavia   Rigamonti Dorotea  

Human Molecular Genetics, Vol. 9, Iss. 19, 2000-11 ,pp. : 2799-2809

Oxford University Press

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Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in Hdh Q92 and Hdh Q111 knock-in mice

By Wheeler Vanessa C.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 503-513

Oxford University Press

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Somatic expansion behaviour of the (CTG) n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch–repair proteins

By te Riele H.   van den Broek W.J.A.A.   Nelen M.R.   Wansink D.G.   Coerwinkel M.M.   Groenen P.J.T.A.   Wieringa B.  

Human Molecular Genetics, Vol. 11, Iss. 2, 2002-01 ,pp. : 191-198

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Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice

By Borchelt D.R.  

Human Molecular Genetics, Vol. 11, Iss. 6, 2002-03 ,pp. : 633-640

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