نتایج جستجو برای: map3k1

تعداد نتایج: 174  

Journal: :Journal of Investigative Dermatology 2021

2017
Sung-Hsin Kuo Shi-Yi Yang San-Lin You Huang-Chun Lien Ching-Hung Lin Po-Han Lin Chiun-Sheng Huang

In this study, we investigated whether single nucleotide polymorphisms (SNPs) identified by genome-wide association study (GWAS) (MAP3K1, FGFR2, TNRC9, HCN1, and 5p12), and SNPs involved in the metabolism of estrogen (CYP19, COMT, ESR1, and UGT1A1), tamoxifen (CYP2C9, CYP2C19, CYP3A5, and CYP2D6), and chemotherapeutic agents (ABCB1, ALDH3A1, and CYP2B6) are associated with the prognoses of 414 ...

Journal: :American journal of human genetics 2008
Antonis C Antoniou Amanda B Spurdle Olga M Sinilnikova Sue Healey Karen A Pooley Rita K Schmutzler Beatrix Versmold Christoph Engel Alfons Meindl Norbert Arnold Wera Hofmann Christian Sutter Dieter Niederacher Helmut Deissler Trinidad Caldes Kati Kämpjärvi Heli Nevanlinna Jacques Simard Jonathan Beesley Xiaoqing Chen Susan L Neuhausen Timothy R Rebbeck Theresa Wagner Henry T Lynch Claudine Isaacs Jeffrey Weitzel Patricia A Ganz Mary B Daly Gail Tomlinson Olufunmilayo I Olopade Joanne L Blum Fergus J Couch Paolo Peterlongo Siranoush Manoukian Monica Barile Paolo Radice Csilla I Szabo Lutecia H Mateus Pereira Mark H Greene Gad Rennert Flavio Lejbkowicz Ofra Barnett-Griness Irene L Andrulis Hilmi Ozcelik Anne-Marie Gerdes Maria A Caligo Yael Laitman Bella Kaufman Roni Milgrom Eitan Friedman Susan M Domchek Katherine L Nathanson Ana Osorio Gemma Llort Roger L Milne Javier Benítez Ute Hamann Frans B L Hogervorst Peggy Manders Marjolijn J L Ligtenberg Ans M W van den Ouweland Susan Peock Margaret Cook Radka Platte D Gareth Evans Rosalind Eeles Gabriella Pichert Carol Chu Diana Eccles Rosemarie Davidson Fiona Douglas Andrew K Godwin Laure Barjhoux Sylvie Mazoyer Hagay Sobol Violaine Bourdon François Eisinger Agnès Chompret Corinne Capoulade Brigitte Bressac-de Paillerets Gilbert M Lenoir Marion Gauthier-Villars Claude Houdayer Dominique Stoppa-Lyonnet Georgia Chenevix-Trench Douglas F Easton

Germline mutations in BRCA1 and BRCA2 confer high risks of breast cancer. However, evidence suggests that these risks are modified by other genetic or environmental factors that cluster in families. A recent genome-wide association study has shown that common alleles at single nucleotide polymorphisms (SNPs) in FGFR2 (rs2981582), TNRC9 (rs3803662), and MAP3K1 (rs889312) are associated with incr...

2017
Jing-Huei Lee Zachary Tucker Maureen Mongan Qinghang Meng Ying Xia

PURPOSE Embryonic eyelid closure is a well-documented morphogenetic episode in mammalian eye development. Detection of eyelid closure defect in humans is a major challenge because eyelid closure and reopen occur entirely in utero. As a consequence, congenital eye defects that are associated with failure of embryonic eyelid closure remain unknown. To fill the gap, we developed a mouse model of d...

Journal: :Nature communications 2011
Hanshuo Zhang Yang Hao Junyu Yang Ying Zhou Juan Li Shenyi Yin Changhong Sun Ming Ma Yanyi Huang Jianzhong Jeff Xi

miRNA globally deregulates human carcinoma. A critical open question is how many miRNAs functionally participate in cancer development, particularly in metastasis. We systematically evaluate the capability of all known human miRNAs to regulate certain metastasis-relevant cell behaviours. To perform the high-throughput screen of miR...

2018
Mev Dominguez-Valentin D Gareth R Evans Sigve Nakken Hélène Tubeuf Daniel Vodak Per Olaf Ekstrøm Anke M Nissen Monika Morak Elke Holinski-Feder Alexandra Martins Pål Møller Eivind Hovig

Background In kindreds carrying path_BRCA1/2 variants, some women in these families will develop cancer despite testing negative for the family's pathogenic variant. These families may have additional genetic variants, which not only may increase the susceptibility of the families' path_BRCA1/2, but also be capable of causing cancer in the absence of the path_BRCA1/2 variants. We aimed to ident...

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