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Results: 1 to 20 of 215

Similar articles for PubMed (Select 16136382)

1.

Lynch syndrome genes.

Peltomäki P.

Fam Cancer. 2005;4(3):227-32. Review.

PMID:
16136382
2.

Advances in the study of Lynch syndrome in China.

Lu JY, Sheng JQ.

World J Gastroenterol. 2015 Jun 14;21(22):6861-6871. Review.

3.

International society for gastrointestinal hereditary tumours-InSiGHT.

[No authors listed]

Fam Cancer. 2015 Jun;14 Suppl 1:1-91. doi: 10.1007/s10689-015-9808-x. No abstract available.

PMID:
25986922
4.

Variation in lynch syndrome.

Church J, Kravochuck S.

Dis Colon Rectum. 2015 May;58(5):e77; quiz e79. doi: 10.1097/DCR.0000000000000355. No abstract available.

PMID:
25850851
5.

Establishing cancer risks associated with PMS2 germline mutations in Lynch syndrome.

Caron NS.

Clin Genet. 2015 Jun;87(6):533-4. doi: 10.1111/cge.12583. Epub 2015 Apr 6. No abstract available.

PMID:
25761717
6.

Milestones of Lynch syndrome: 1895-2015.

Lynch HT, Snyder CL, Shaw TG, Heinen CD, Hitchins MP.

Nat Rev Cancer. 2015 Mar;15(3):181-94. doi: 10.1038/nrc3878. Epub 2015 Feb 12.

PMID:
25673086
7.

Glioblastomas, astrocytomas and oligodendrogliomas linked to Lynch syndrome.

Therkildsen C, Ladelund S, Rambech E, Persson A, Petersen A, Nilbert M.

Eur J Neurol. 2015 Apr;22(4):717-24. doi: 10.1111/ene.12647. Epub 2015 Jan 19.

PMID:
25648859
8.

DNA mismatch repair enzymes: genetic defects and autoimmunity.

Muro Y, Sugiura K, Mimori T, Akiyama M.

Clin Chim Acta. 2015 Mar 10;442:102-9. doi: 10.1016/j.cca.2015.01.014. Epub 2015 Jan 22. Review.

PMID:
25619773
9.

Guidelines on genetic evaluation and management of Lynch syndrome.

Dinjens WN, Dubbink HJ, Wagner A.

Am J Gastroenterol. 2015 Jan;110(1):192-3. doi: 10.1038/ajg.2014.329. No abstract available.

PMID:
25567172
10.

Clearer picture of PMS2-associated lynch syndrome is emerging.

Daniels MS, Lu KH.

J Clin Oncol. 2015 Feb 1;33(4):299-300. doi: 10.1200/JCO.2014.58.9796. Epub 2014 Dec 22. No abstract available.

PMID:
25534383
11.

Guidelines on genetic evaluation and management of Lynch syndrome.

Dinjens WN, Dubbink HJ, Wagner A.

Gastrointest Endosc. 2015 Jan;81(1):243-4. doi: 10.1016/j.gie.2014.10.014. No abstract available.

PMID:
25527063
12.

Role of endometrial cancer abnormal MMR protein in screening Lynch-syndrome families.

Long Q, Peng Y, Tang Z, Wu C.

Int J Clin Exp Pathol. 2014 Sep 15;7(10):7297-303. eCollection 2014.

13.

Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome.

Ponti G, Castellsagué E, Ruini C, Percesepe A, Tomasi A.

Clin Genet. 2015 Jun;87(6):507-16. doi: 10.1111/cge.12529. Epub 2014 Dec 9.

PMID:
25345868
14.

Localization of MLH3 at the centrosomes.

Roesner LM, Mielke C, Faehnrich S, Merkhoffer Y, Dittmar KE, Drexler HG, Dirks WG.

Int J Mol Sci. 2014 Aug 11;15(8):13932-7. doi: 10.3390/ijms150813932.

15.

BluepRINT for moderate-to-low penetrance cancer susceptibility genes needed: breast cancer and beyond.

Ngeow J, Eng C.

Cancer Discov. 2014 Jul;4(7):762-3. doi: 10.1158/2159-8290.CD-14-0498.

16.

A review of mismatch repair gene transcripts: issues for interpretation of mRNA splicing assays.

Thompson BA, Martins A, Spurdle AB.

Clin Genet. 2015 Feb;87(2):100-8. doi: 10.1111/cge.12450. Epub 2014 Jul 26.

PMID:
24989436
17.

Biochemical characterization of a cancer-associated E109K missense variant of human exonuclease 1.

Bregenhorn S, Jiricny J.

Nucleic Acids Res. 2014 Jun;42(11):7096-103. doi: 10.1093/nar/gku419. Epub 2014 May 14.

18.

Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'care for CMMRD' (C4CMMRD).

Wimmer K, Kratz CP, Vasen HF, Caron O, Colas C, Entz-Werle N, Gerdes AM, Goldberg Y, Ilencikova D, Muleris M, Duval A, Lavoine N, Ruiz-Ponte C, Slavc I, Burkhardt B, Brugieres L; EU-Consortium Care for CMMRD (C4CMMRD).

J Med Genet. 2014 Jun;51(6):355-65. doi: 10.1136/jmedgenet-2014-102284. Epub 2014 Apr 15. Review.

PMID:
24737826
19.

A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes.

Hansen MF, Neckmann U, Lavik LA, Vold T, Gilde B, Toft RK, Sjursen W.

Mol Genet Genomic Med. 2014 Mar;2(2):186-200. doi: 10.1002/mgg3.62. Epub 2014 Jan 21.

20.

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

Thompson BA, Spurdle AB, Plazzer JP, Greenblatt MS, Akagi K, Al-Mulla F, Bapat B, Bernstein I, Capellá G, den Dunnen JT, du Sart D, Fabre A, Farrell MP, Farrington SM, Frayling IM, Frebourg T, Goldgar DE, Heinen CD, Holinski-Feder E, Kohonen-Corish M, Robinson KL, Leung SY, Martins A, Moller P, Morak M, Nystrom M, Peltomaki P, Pineda M, Qi M, Ramesar R, Rasmussen LJ, Royer-Pokora B, Scott RJ, Sijmons R, Tavtigian SV, Tops CM, Weber T, Wijnen J, Woods MO, Macrae F, Genuardi M; InSiGHT.

Nat Genet. 2014 Feb;46(2):107-15. doi: 10.1038/ng.2854. Epub 2013 Dec 22.

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