Documents (102) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
PubMed	16837128	Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations. He	2.05 KB	2020-01-28	10	-
PubMed	17054581	Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population w	2.79 KB	2015-12-25	8	-
PubMed	17409200	Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington d	1.67 KB	2019-11-01	6	-
PubMed	17715336	Longitudinal evaluation of the Hdh(CAG)150 knock-in murine model of Huntington's disease. Several mu	1.29 KB	2020-01-28	9	-
PubMed	18057311	Comparative analysis of meiotic progression in female mice bearing mutations in genes of the DNA mis	1.73 KB	2020-02-21	6	-
PubMed	18206535	Somatic mutations in mismatch repair genes in sporadic gastric carcinomas are not a cause but a cons	1.35 KB	2020-02-21	6	-
PubMed	18412970	Elucidating a normal function of huntingtin by functional and microarray analysis of huntingtin-null	2.35 KB	2019-11-01	8	-
PubMed	18505871	A mutation in the putative MLH3 endonuclease domain confers a defect in both mismatch repair and mei	1.51 KB	2020-01-28	8	-
PubMed	18551179	Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastroi	1.75 KB	2015-11-24	10	-
PubMed	18787700	Human MLH1 protein participates in genomic damage checkpoint signaling in response to DNA interstran	1.88 KB	2019-11-01	7	-