62 related articles for article (PubMed ID: 16706114)
21. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):536. PubMed ID: 15991308
[No Abstract] [Full Text] [Related]
22. Mechanisms of pathogenicity in human MSH2 missense mutants.
Ollila S; Dermadi Bebek D; Jiricny J; Nyström M
Hum Mutat; 2008 Nov; 29(11):1355-63. PubMed ID: 18951462
[TBL] [Abstract][Full Text] [Related]
23. Gene symbol: hMSH2. Disease: hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 Dec; 118(3-4):546. PubMed ID: 16521300
[No Abstract] [Full Text] [Related]
24. Solitary subungual keratoacanthoma arising in an MSH2 germline mutation carrier: confirmation of a relationship by immunohistochemical analysis.
Stoebner PE; Fabre C; Delfour C; Joujoux JM; Roger P; Dandurand M; Meunier L
Dermatology; 2009; 219(2):174-8. PubMed ID: 19602866
[TBL] [Abstract][Full Text] [Related]
25. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):538. PubMed ID: 15991314
[No Abstract] [Full Text] [Related]
26. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):410. PubMed ID: 15046099
[No Abstract] [Full Text] [Related]
27. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046096
[No Abstract] [Full Text] [Related]
28. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):409. PubMed ID: 15046093
[No Abstract] [Full Text] [Related]
29. Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Sun MH; Cai Q; Fu G; Ren S; Mo S; Xu Y; Ding C; Zhang T; Zhu X; Xu X; Min D; Cai S; Luo D; Shi Y; Shi D
Hum Genet; 2004 Mar; 114(4):408. PubMed ID: 15046091
[No Abstract] [Full Text] [Related]
30. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Corish MR
Hum Genet; 2005 May; 116(6):538. PubMed ID: 15991315
[No Abstract] [Full Text] [Related]
31. Gene symbol: MSH2. Disease: Hereditary nonpolyposis colorectal cancer.
Otway R; Tetlow N; Hornby J; Doe WF; Kohonen-Coriah MR
Hum Genet; 2005 May; 116(6):539. PubMed ID: 15991316
[No Abstract] [Full Text] [Related]
32. MutS as a tool for mutation detection.
Stanisławska-Sachadyn A; Sachadyn P
Acta Biochim Pol; 2005; 52(3):575-83. PubMed ID: 16082411
[TBL] [Abstract][Full Text] [Related]
33. [A simple and rapid method for detection of the 106Gln mutation in Wilson-Konovalov disease].
Shadrina MI; Slominskiĭ PA; Karabanov AV; Ivanova-Smolenskaia IA; Limborskaia SA
Genetika; 2002 Dec; 38(12):1723-5. PubMed ID: 12575461
[TBL] [Abstract][Full Text] [Related]
34. Development of a Premature Stop Codon-detection method based on a bacterial two-hybrid system.
Real SM; Marzese DM; Gomez LC; Mayorga LS; Roqué M
BMC Biotechnol; 2006 Sep; 6():38. PubMed ID: 16948859
[TBL] [Abstract][Full Text] [Related]
35. Orphan peak analysis: a novel method for detection of point mutations using an automated fluorescence DNA sequencer.
Hattori M; Shibata A; Yoshioka K; Sakaki Y
Genomics; 1993 Feb; 15(2):415-7. PubMed ID: 8449509
[TBL] [Abstract][Full Text] [Related]
36. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer.
Fishel R; Lescoe MK; Rao MR; Copeland NG; Jenkins NA; Garber J; Kane M; Kolodner R
Cell; 1994 Apr; 77(1):1 p following 166. PubMed ID: 8156592
[No Abstract] [Full Text] [Related]
37. Towards automatic detection of point mutations: use of scintillating microplates in solid-phase minisequencing.
Ihalainen J; Siitari H; Laine S; Syvänen AC; Palotie A
Biotechniques; 1994 May; 16(5):938-43. PubMed ID: 8068351
[TBL] [Abstract][Full Text] [Related]
38. Papillary serous carcinoma in situ in ovarian endometriosis in an MSH2 mutation carrier.
Vaknin Z; Gotlieb WH; Arseneau J; Ferenczy A
Int J Gynaecol Obstet; 2009 Oct; 107(1):68-9. PubMed ID: 19545867
[No Abstract] [Full Text] [Related]
39. DGGE polymorphism in intron 10 of MSH2, the HNPCC gene.
Wijnen J; Fodde R; Khan PM
Hum Mol Genet; 1994 Dec; 3(12):2268. PubMed ID: 7881445
[No Abstract] [Full Text] [Related]
40. Doublex sequencing in molecular diagnosis of hereditary diseases.
Plaschke J; Voss H; Hahn M; Ansorge W; Schackert HK
Biotechniques; 1998 May; 24(5):838-41. PubMed ID: 9591136
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]