Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 274

Similar articles for PubMed (Select 11781295)

1.

Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system.

Trojan J, Zeuzem S, Randolph A, Hemmerle C, Brieger A, Raedle J, Plotz G, Jiricny J, Marra G.

Gastroenterology. 2002 Jan;122(1):211-9.

PMID:
11781295
2.

Intronic and promoter polymorphisms of hMLH1/hMSH2 and colorectal cancer risk in Heilongjiang Province of China.

Li G, Hu F, Yuan F, Fan J, Yu Z, Wu Z, Zhao X, Li Y, Li S, Rong J, Cui B, Dong X, Yuan H, Zhao Y.

J Cancer Res Clin Oncol. 2015 Aug;141(8):1393-404. doi: 10.1007/s00432-014-1898-6. Epub 2015 Jan 6.

PMID:
25560462
3.

Phenotypic characterization of missense polymerase-δ mutations using an inducible protein-replacement system.

Ghodgaonkar MM, Kehl P, Ventura I, Hu L, Bignami M, Jiricny J.

Nat Commun. 2014 Sep 22;5:4990. doi: 10.1038/ncomms5990.

PMID:
25241845
4.

Mismatch repair protein expression in colorectal cancer.

Kheirelseid EA, Miller N, Chang KH, Curran C, Hennessey E, Sheehan M, Kerin MJ.

J Gastrointest Oncol. 2013 Dec;4(4):397-408. doi: 10.3978/j.issn.2078-6891.2013.021.

5.

Expression of the mismatch repair gene hMLH1 is enhanced in non-small cell lung cancer with EGFR mutations.

Li M, Zhang Q, Liu L, Lu W, Wei H, Li RW, Lu S.

PLoS One. 2013 Oct 24;8(10):e78500. doi: 10.1371/journal.pone.0078500. eCollection 2013.

6.

[Establishment of a hMSH2/hMSH6 protein interaction system and functional evaluation of hMSH2 gene missense mutations].

Zhu M, Fan YM, Zhu YB, Wang YP.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Oct;30(5):559-64. doi: 10.3760/cma.j.issn.1003-9406.2013.05.011. Chinese.

PMID:
24078570
7.

Naturally occurring HCA1 missense mutations result in loss of function: potential impact on lipid deposition.

Doyle JR, Lane JM, Beinborn M, Kopin AS.

J Lipid Res. 2013 Mar;54(3):823-30. doi: 10.1194/jlr.M034660. Epub 2012 Dec 24.

8.

Implication of DNA repair genes in prostate tumourigenesis in Indian males.

Bansal A, Soni A, Rao P, Singh LC, Mishra AK, Mohanty NK, Saxena S.

Indian J Med Res. 2012 Oct;136(4):622-32.

9.

Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats.

Panigrahi GB, Slean MM, Simard JP, Pearson CE.

J Biol Chem. 2012 Dec 7;287(50):41844-50. doi: 10.1074/jbc.M112.420398. Epub 2012 Oct 18.

10.

Sub-cellular localization analysis of MSH6 missense mutations does not reveal an overt MSH6 nuclear transport impairment.

Belvederesi L, Bianchi F, Loretelli C, Bracci R, Cascinu S, Cellerino R.

Fam Cancer. 2012 Dec;11(4):675-80. doi: 10.1007/s10689-012-9558-y.

PMID:
22851212
11.

Pathological assessment of mismatch repair gene variants in Lynch syndrome: past, present, and future.

Rasmussen LJ, Heinen CD, Royer-Pokora B, Drost M, Tavtigian S, Hofstra RM, de Wind N.

Hum Mutat. 2012 Dec;33(12):1617-25. doi: 10.1002/humu.22168. Epub 2012 Aug 13. Review.

PMID:
22833534
12.

Determining the functional significance of mismatch repair gene missense variants using biochemical and cellular assays.

Heinen CD, Juel Rasmussen L.

Hered Cancer Clin Pract. 2012 Jul 23;10(1):9. doi: 10.1186/1897-4287-10-9.

13.

A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome.

Bergman JE, Janssen N, van der Sloot AM, de Walle HE, Schoots J, Rendtorff ND, Tranebjaerg L, Hoefsloot LH, van Ravenswaaij-Arts CM, Hofstra RM.

Hum Mutat. 2012 Aug;33(8):1251-60. doi: 10.1002/humu.22106. Epub 2012 May 11.

PMID:
22539353
14.

Effects of hyperthermia on Hsp27 (HSPB1), Hsp72 (HSPA1A) and DNA repair proteins hMLH1 and hMSH2 in human colorectal cancer hMLH1-deficient and hMLH1-proficient cell lines.

Nadin SB, Cuello-Carrión FD, Sottile ML, Ciocca DR, Vargas-Roig LM.

Int J Hyperthermia. 2012;28(3):191-201. doi: 10.3109/02656736.2011.638962.

PMID:
22515340
15.

Classification of mismatch repair gene missense variants with PON-MMR.

Ali H, Olatubosun A, Vihinen M.

Hum Mutat. 2012 Apr;33(4):642-50. doi: 10.1002/humu.22038.

PMID:
22290698
16.

Detection of variants in SLC6A8 and functional analysis of unclassified missense variants.

Betsalel OT, Pop A, Rosenberg EH, Fernandez-Ojeda M; Creatine Transporter Research, Group, Jakobs C, Salomons GS.

Mol Genet Metab. 2012 Apr;105(4):596-601. doi: 10.1016/j.ymgme.2011.12.022. Epub 2012 Jan 6.

PMID:
22281021
17.
18.

Influence of eight unclassified missense variants of the MLH1 gene on Lynch syndrome susceptibility.

Fan Y, Chen J, Wang W, Wu P, Zhi W, Xue B, Zhang W, Wang Y.

Biochem Genet. 2012 Feb;50(1-2):84-93. doi: 10.1007/s10528-011-9467-z. Epub 2011 Sep 28.

PMID:
21952876
19.

[Effect of estrogen on mismatch repair gene expression in colon cancer cells].

Lu XJ, Yu DL, Wang JX, Pan XL, Jin P, Li SR, Sheng JQ.

Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2011 Jul;27(7):754-6. Chinese.

PMID:
21722527
20.

Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies.

Hardt K, Heick SB, Betz B, Goecke T, Yazdanparast H, Küppers R, Servan K, Steinke V, Rahner N, Morak M, Holinski-Feder E, Engel C, Möslein G, Schackert HK, von Knebel Doeberitz M, Pox C; Peter Propping; German HNPCC consortium, Hegemann JH, Royer-Pokora B.

Fam Cancer. 2011 Jun;10(2):273-84. doi: 10.1007/s10689-011-9431-4.

PMID:
21404117
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk