A functional assay for mutations in tumor suppressor genes caused by mismatch repair deficiency

By Ji H.P.   King M-C.  

Human Molecular Genetics, Vol. 10, Iss. 24, 2001-11 ,pp. : 2737-2743

Oxford University Press

Access to resources Recommend Favorite

DNMT1 deficiency triggers mismatch repair defects in human cells through depletion of repair protein levels in a process involving the DNA damage response

By Loughery Jayne E.P.   Dunne Philip D.   O'Neill Karla M.   Meehan Richard R.   McDaid Jennifer R.   Walsh Colum P.  

Human Molecular Genetics, Vol. 20, Iss. 16, 2011-08 ,pp. : 3241-3255

Oxford University Press

Access to resources Recommend Favorite

Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses

By  

Molecular Genetics & Genomic Medicine, Vol. 3, Iss. 4, 2015-07 ,pp. : 327-345

John Wiley & Sons Inc

Access to resources Recommend Favorite

Defects in homologous recombination repair in mismatch-repair-deficient tumour cell lines

By Mohindra A.  

Human Molecular Genetics, Vol. 11, Iss. 18, 2002-06 ,pp. : 2189-2200

Oxford University Press

Access to resources Recommend Favorite

In memory of S.I. Alikhanyan—The great is better seen from far away

By Krylov V.  

Russian Journal of Genetics, Vol. 42, Iss. 11, 2006-11 ,pp. : 1245-1256

MAIK Nauka/Interperiodica

Access to resources Recommend Favorite