The relationships between somatic mutation of hMLH1/hMSH2 gene and clinicopathological features of the 342 sporadic CRC patients.

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

Oliveira, C.
Westra, J.
Arango, D.
Ollikainen, M.
Domingo, E.
Ferreira, A.
Velho, S.
Niessen, R.
Lagerstedt, K.
Alhopuro, P.
Laiho, P.
Veiga, I.
Teixeira, M.R.
Ligtenberg, M.J.L.
Kleibeuker, J.H.
Sijmons, R.H.
Plukker, J.T.
Imai, K.
Lage, P.
Hamelin, R.
Albuquerque, C.
Schwartz Jr, S.
Lindblom, A.
Peltomaki, P.
Yamamoto, H.
Aaltonen, L.A.
Seruca, R.
Hofstra, R.M.

January 2004

Contains fulltext : 57104.pdf (publisher's version ) (Closed access)In sporadic co...

DNA variants found in hMLH1 and hMSH2 genes.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

*DNA variant found in the relapse tumor of a LS CRC patient.‡The variants were detected in...

The association between genetic variants in <it>hMLH1 </it>and <it>hMSH2 </it>and the development of sporadic colorectal cancer in the Danish population

Syvänen Ann-Christine
Olsen Anja
Tjønneland Anne
Koed Karen
Wiuf Carsten
Wikman Friedrik P
Madsen Bo E
Christensen Lise
Andersen Claus L
Ørntoft Torben F

June 2008

Abstract Background Mutations in the mismatch repair genes hMLH1 and hMSH2 predispose to hereditary ...

The relationships between germline mutation of hMLH1/hMSH2 gene and clinicopathological features of the 436 sporadic CRC patients.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

The relationships between germline mutation of hMLH1/hMSH2 gene and clinicopathological fe...

Mutation frequencies of hMLH1 and hMSH2 genes.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

†The mutation was also found in another blood sample of LS relapsed CRC patient.††One pati...

Novel DNA variants and mutation frequencies of hMLH1 and hMSH2 genes in colorectal cancer in the Northeast China population.

Fulan Hu
Dandan Li
Yibaina Wang
Xiaoping Yao
Wencui Zhang
Jing Liang
Chunqing Lin
Jiaojiao Ren
Lin Zhu
Zhiwei Wu
Shuying Li
Ye Li
Xiaojuan Zhao
Binbin Cui
Xinshu Dong
Suli Tian
Yashuang Zhao

Research on hMLH1 and hMSH2 mutations tend to focus on Lynch syndrome (LS) and LS-like colorectal ca...

Novel DNA Variants and Mutation Frequencies of hMLH1 and hMSH2 Genes in Colorectal Cancer in the Northeast China Population

Fulan Hu
An Li
Yibaina Wang
Xiaoping Yao
Wencui Zhang
Jing Liang
Chunqing Lin
Jiaojiao Ren
Lin Zhu
Zhiwei Wu
Shuying Li
Ye Li
Xiaojuan Zhao
Binbin Cui
Xinshu Dong
Suli Tian Yashuang

August 2016

Research on hMLH1 and hMSH2 mutations tend to focus on Lynch syndrome (LS) and LS-like colorectal ca...

Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.

Wenzhen Xia (14237334)
Zhaoyu Gao (14237337)
Xia Jiang (210366)
Lei Jiang (73366)
Yushi Qin (14237340)
Di Zhang (197959)
Pei Tian (783540)
Wanchang Wang (14237343)
Qi Zhang (28502)
Rui Zhang (13940)
Nan Zhang (46264)
Shunjiang Xu (14237346)

December 2022

Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.</p

Frequency of co-occurring genetic alterations in FERMT2, SYNE1, FAT4 and MUC16, and the correlation between FERMT2 with SYNE1, FAT4 or MUC16 in CRC patients (cBioPortal).

Wenzhen Xia (14237334)
Zhaoyu Gao (14237337)
Xia Jiang (210366)
Lei Jiang (73366)
Yushi Qin (14237340)
Di Zhang (197959)
Pei Tian (783540)
Wanchang Wang (14237343)
Qi Zhang (28502)
Rui Zhang (13940)
Nan Zhang (46264)
Shunjiang Xu (14237346)

December 2022

(A, B) OncoPrint of FERMT2 co-occurring alterations in CRC cohort. The different types of genetic al...

Prevalence of hMLH1 and hMSH2 gene germline mutation in different exons.

Dandan Li (391591)
Fulan Hu (391592)
Fan Wang (135182)
Binbin Cui (194032)
Xinshu Dong (391593)
Wencui Zhang (391594)
Chunqing Lin (391595)
Xia Li (14984)
Da Wang (347990)
Yashuang Zhao (391596)

March 2013

Prevalence of hMLH1 and hMSH2 gene germline mutation in different exons.</p

Percentage of shared point mutations in CRC-CLM pairs.

Sun Young Lee (530814)
Farhan Haq (530815)
Deokhoon Kim (212912)
Cui Jun (530816)
Hui-Jong Jo (530817)
Sung-Min Ahn (212964)
Won-Suk Lee (530818)

March 2014

*It indicates whether primary CRCs and their matched CLMs are most closely related in the hierarc...

Molecular genetic studies of colorectal cancer

Zhou, Xiaolei

October 2005

Colorectal cancer (CRC) is one of the leading causes of morbidity and mortality due to cancer in the...

Mutations in MLH1 gene and MSI status as molecular characteristics of sporadic colorectal cancer

Čaja, Fabián

January 2017

Colorectal carcinoma (CRC) is one of the most prevalent malignancies in the Czech Republic. In gener...

Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: Correlation with microsatellite instability and abnormalities of mismatch repair protein expression

Scartozzi, Mario
Bianchi, F
Rosati, S
Galizia, E
Antolini, A
Loretelli, C
Piga, A
Bearzi, I
Cellerino, R
Porfiri, E.

January 2002

Purpose: The relationship between germ-line mutations of hMSH2 and hMLH1, microsatellite instability...

Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

Raffaella Liccardo
De Rosa Marina
Duraturo Francesca

January 2018

Lynch syndrome is an autosomal dominant syndrome that can be subdivided into Lynch syndrome I, or si...

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

Oliveira, C.
Westra, J.
Arango, D.
Ollikainen, M.
Domingo, E.
Ferreira, A.
Velho, S.
Niessen, R.
Lagerstedt, K.
Alhopuro, P.
Laiho, P.
Veiga, I.
Teixeira, M.R.
Ligtenberg, M.J.L.
Kleibeuker, J.H.
Sijmons, R.H.
Plukker, J.T.
Imai, K.
Lage, P.
Hamelin, R.
Albuquerque, C.
Schwartz Jr, S.
Lindblom, A.
Peltomaki, P.
Yamamoto, H.
Aaltonen, L.A.
Seruca, R.
Hofstra, R.M.

January 2004

Contains fulltext : 57104.pdf (publisher's version ) (Closed access)In sporadic co...

DNA variants found in hMLH1 and hMSH2 genes.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

*DNA variant found in the relapse tumor of a LS CRC patient.‡The variants were detected in...

The association between genetic variants in <it>hMLH1 </it>and <it>hMSH2 </it>and the development of sporadic colorectal cancer in the Danish population

Syvänen Ann-Christine
Olsen Anja
Tjønneland Anne
Koed Karen
Wiuf Carsten
Wikman Friedrik P
Madsen Bo E
Christensen Lise
Andersen Claus L
Ørntoft Torben F

June 2008

Abstract Background Mutations in the mismatch repair genes hMLH1 and hMSH2 predispose to hereditary ...

The relationships between germline mutation of hMLH1/hMSH2 gene and clinicopathological features of the 436 sporadic CRC patients.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

The relationships between germline mutation of hMLH1/hMSH2 gene and clinicopathological fe...

Mutation frequencies of hMLH1 and hMSH2 genes.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

†The mutation was also found in another blood sample of LS relapsed CRC patient.††One pati...

Novel DNA variants and mutation frequencies of hMLH1 and hMSH2 genes in colorectal cancer in the Northeast China population.

Fulan Hu
Dandan Li
Yibaina Wang
Xiaoping Yao
Wencui Zhang
Jing Liang
Chunqing Lin
Jiaojiao Ren
Lin Zhu
Zhiwei Wu
Shuying Li
Ye Li
Xiaojuan Zhao
Binbin Cui
Xinshu Dong
Suli Tian
Yashuang Zhao

Research on hMLH1 and hMSH2 mutations tend to focus on Lynch syndrome (LS) and LS-like colorectal ca...

Novel DNA Variants and Mutation Frequencies of hMLH1 and hMSH2 Genes in Colorectal Cancer in the Northeast China Population

Fulan Hu
An Li
Yibaina Wang
Xiaoping Yao
Wencui Zhang
Jing Liang
Chunqing Lin
Jiaojiao Ren
Lin Zhu
Zhiwei Wu
Shuying Li
Ye Li
Xiaojuan Zhao
Binbin Cui
Xinshu Dong
Suli Tian Yashuang

August 2016

Research on hMLH1 and hMSH2 mutations tend to focus on Lynch syndrome (LS) and LS-like colorectal ca...

Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.

Wenzhen Xia (14237334)
Zhaoyu Gao (14237337)
Xia Jiang (210366)
Lei Jiang (73366)
Yushi Qin (14237340)
Di Zhang (197959)
Pei Tian (783540)
Wanchang Wang (14237343)
Qi Zhang (28502)
Rui Zhang (13940)
Nan Zhang (46264)
Shunjiang Xu (14237346)

December 2022

Frequency of co-occurring genomic alterations associated with FERMT2 in patients with CRC.</p

Frequency of co-occurring genetic alterations in FERMT2, SYNE1, FAT4 and MUC16, and the correlation between FERMT2 with SYNE1, FAT4 or MUC16 in CRC patients (cBioPortal).

Wenzhen Xia (14237334)
Zhaoyu Gao (14237337)
Xia Jiang (210366)
Lei Jiang (73366)
Yushi Qin (14237340)
Di Zhang (197959)
Pei Tian (783540)
Wanchang Wang (14237343)
Qi Zhang (28502)
Rui Zhang (13940)
Nan Zhang (46264)
Shunjiang Xu (14237346)

December 2022

(A, B) OncoPrint of FERMT2 co-occurring alterations in CRC cohort. The different types of genetic al...

Prevalence of hMLH1 and hMSH2 gene germline mutation in different exons.

Dandan Li (391591)
Fulan Hu (391592)
Fan Wang (135182)
Binbin Cui (194032)
Xinshu Dong (391593)
Wencui Zhang (391594)
Chunqing Lin (391595)
Xia Li (14984)
Da Wang (347990)
Yashuang Zhao (391596)

March 2013

Prevalence of hMLH1 and hMSH2 gene germline mutation in different exons.</p

Percentage of shared point mutations in CRC-CLM pairs.

Sun Young Lee (530814)
Farhan Haq (530815)
Deokhoon Kim (212912)
Cui Jun (530816)
Hui-Jong Jo (530817)
Sung-Min Ahn (212964)
Won-Suk Lee (530818)

March 2014

*It indicates whether primary CRCs and their matched CLMs are most closely related in the hierarc...

Molecular genetic studies of colorectal cancer

Zhou, Xiaolei

October 2005

Colorectal cancer (CRC) is one of the leading causes of morbidity and mortality due to cancer in the...

Mutations in MLH1 gene and MSI status as molecular characteristics of sporadic colorectal cancer

Čaja, Fabián

January 2017

Colorectal carcinoma (CRC) is one of the most prevalent malignancies in the Czech Republic. In gener...

Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: Correlation with microsatellite instability and abnormalities of mismatch repair protein expression

Scartozzi, Mario
Bianchi, F
Rosati, S
Galizia, E
Antolini, A
Loretelli, C
Piga, A
Bearzi, I
Cellerino, R
Porfiri, E.

January 2002

Purpose: The relationship between germ-line mutations of hMSH2 and hMLH1, microsatellite instability...

Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

Raffaella Liccardo
De Rosa Marina
Duraturo Francesca

January 2018

Lynch syndrome is an autosomal dominant syndrome that can be subdivided into Lynch syndrome I, or si...

Distinct patterns of KRAS mutations in colorectal carcinomas according to germline mismatch repair defects and hMLH1 methylation status.

Oliveira, C.
Westra, J.
Arango, D.
Ollikainen, M.
Domingo, E.
Ferreira, A.
Velho, S.
Niessen, R.
Lagerstedt, K.
Alhopuro, P.
Laiho, P.
Veiga, I.
Teixeira, M.R.
Ligtenberg, M.J.L.
Kleibeuker, J.H.
Sijmons, R.H.
Plukker, J.T.
Imai, K.
Lage, P.
Hamelin, R.
Albuquerque, C.
Schwartz Jr, S.
Lindblom, A.
Peltomaki, P.
Yamamoto, H.
Aaltonen, L.A.
Seruca, R.
Hofstra, R.M.

January 2004

Contains fulltext : 57104.pdf (publisher's version ) (Closed access)In sporadic co...

DNA variants found in hMLH1 and hMSH2 genes.

Fulan Hu (391592)
Dandan Li (391591)
Yibaina Wang (396583)
Xiaoping Yao (396582)
Wencui Zhang (391594)
Jing Liang (32441)
Chunqing Lin (391595)
Jiaojiao Ren (397881)
Lin Zhu (192179)
Zhiwei Wu (324485)
Shuying Li (354398)
Ye Li (290115)
Xiaojuan Zhao (328276)
Binbin Cui (194032)
Xinshu Dong (391593)
Suli Tian (397882)
Yashuang Zhao (391596)

April 2013

*DNA variant found in the relapse tumor of a LS CRC patient.‡The variants were detected in...

The association between genetic variants in <it>hMLH1 </it>and <it>hMSH2 </it>and the development of sporadic colorectal cancer in the Danish population

Syvänen Ann-Christine
Olsen Anja
Tjønneland Anne
Koed Karen
Wiuf Carsten
Wikman Friedrik P
Madsen Bo E
Christensen Lise
Andersen Claus L
Ørntoft Torben F

June 2008

Abstract Background Mutations in the mismatch repair genes hMLH1 and hMSH2 predispose to hereditary ...

The relationships between somatic mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological features of the 342 sporadic CRC patients.

Abstract

Extracted data

The relationships between somatic mutation of <i>hMLH1/hMSH2</i> gene and clinicopathological features of the 342 sporadic CRC patients.

Abstract

Extracted data

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