Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Craig Chinault, A."'
Autor:
Timothy C. Thompson, Terry L. Timme, Wei-Wen Cai, A. Craig Chinault, Alexei A. Goltsov, Guang Yang, Chengzhen Ren, Guangwen Cao, ElMoataz Abdel Fattah, Likun Li
Glioma pathogenesis-related protein 1 (GLIPR1), a novel p53 target gene, is down-regulated by methylation in prostate cancer and has p53-dependent and -independent proapoptotic activities in tumor cells. These properties suggest an important tumor su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93aac3cfba1171f696cf24cdcd5afc44
https://doi.org/10.1158/0008-5472.c.6497183.v1
https://doi.org/10.1158/0008-5472.c.6497183.v1
Autor:
Timothy C. Thompson, Terry L. Timme, Wei-Wen Cai, A. Craig Chinault, Alexei A. Goltsov, Guang Yang, Chengzhen Ren, Guangwen Cao, ElMoataz Abdel Fattah, Likun Li
Supplementary Materials and Methods from Glioma Pathogenesis-Related Protein 1 Exerts Tumor Suppressor Activities through Proapoptotic Reactive Oxygen Species–c-Jun–NH2 Kinase Signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5089dbee80072f5bbc0230a2cd7896c1
https://doi.org/10.1158/0008-5472.22373726
https://doi.org/10.1158/0008-5472.22373726
Autor:
Timothy C. Thompson, Terry L. Timme, Wei-Wen Cai, A. Craig Chinault, Alexei A. Goltsov, Guang Yang, Chengzhen Ren, Guangwen Cao, ElMoataz Abdel Fattah, Likun Li
Supplementary Figure Legends 1-5 from Glioma Pathogenesis-Related Protein 1 Exerts Tumor Suppressor Activities through Proapoptotic Reactive Oxygen Species–c-Jun–NH2 Kinase Signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6925363c23b2ab86dcf60be3a6b10554
https://doi.org/10.1158/0008-5472.22373732
https://doi.org/10.1158/0008-5472.22373732
Autor:
Timothy C. Thompson, Terry L. Timme, Wei-Wen Cai, A. Craig Chinault, Alexei A. Goltsov, Guang Yang, Chengzhen Ren, Guangwen Cao, ElMoataz Abdel Fattah, Likun Li
Supplementary Figures 1-5 from Glioma Pathogenesis-Related Protein 1 Exerts Tumor Suppressor Activities through Proapoptotic Reactive Oxygen Species–c-Jun–NH2 Kinase Signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0132f3b637e12cbc9c78a278910dcbfd
https://doi.org/10.1158/0008-5472.22373729
https://doi.org/10.1158/0008-5472.22373729
Autor:
R Alan Harris, Chad Shaw, Jian Li, Sau Wai Cheung, Cristian Coarfa, Mira Jeong, Margaret A Goodell, Lisa D White, Ankita Patel, Sung-Hae Kang, A Craig Chinault, Tomasz Gambin, Anna Gambin, James R Lupski, Aleksandar Milosavljevic
Publikováno v:
PLoS Genetics, Vol 9, Iss 2, p e1003333 (2013)
Externí odkaz:
https://doaj.org/article/42f726a25e3e4645aad46ac1766b7ca7
Autor:
Jian Li, R Alan Harris, Sau Wai Cheung, Cristian Coarfa, Mira Jeong, Margaret A Goodell, Lisa D White, Ankita Patel, Sung-Hae Kang, Chad Shaw, A Craig Chinault, Tomasz Gambin, Anna Gambin, James R Lupski, Aleksandar Milosavljevic
Publikováno v:
PLoS Genetics, Vol 8, Iss 5, p e1002692 (2012)
The hotspots of structural polymorphisms and structural mutability in the human genome remain to be explained mechanistically. We examine associations of structural mutability with germline DNA methylation and with non-allelic homologous recombinatio
Externí odkaz:
https://doaj.org/article/41f8edd87ece4f28b8c093a59f15c7fa
Autor:
Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino, Pawel Stankiewicz, Zhishu Ou, A Craig Chinault, Arthur L Beaudet, James R Lupski, Sau W Cheung, Patricia A Ward
Publikováno v:
PLoS ONE, Vol 2, Iss 3, p e327 (2007)
BACKGROUND: Array Comparative Genomic Hybridization (a-CGH) is a powerful molecular cytogenetic tool to detect genomic imbalances and study disease mechanism and pathogenesis. We report our experience with the clinical implementation of this high res
Externí odkaz:
https://doaj.org/article/2729b6231a9b4992a3937c4112d5c4e6
Autor:
Mariah R. Baker, Lorraine Potocki, Luis A. Umaña, Luis M. Franco, Gladys Zapata, Stephanie M. Ware, Susan D. Fernbach, Ankita Patel, Miao Huang, Barbara A. Boggs, A. Craig Chinault, Xueqing Wang, John W. Belmont, Zhengxin Jiang, Kristine L. Bucasas, Seema R. Lalani, Ashley Cast, Molly S. Bray, Neil A. Hanchard, Daryl A. Scott, Susan L. Hamilton, Sau Wai Cheung, Qi Tian, John L. Jefferies, Philippe M. Campeau, J.A. Towbin, Kim L. McBride
Publikováno v:
Human Molecular Genetics. 22:4339-4348
Coarctation of the aorta (CoA) and hypoplastic left heart syndrome (HLHS) have been reported in rare individuals with large terminal deletions of chromosome 15q26. However, no single gene important for left ventricular outflow tract (LVOT) developmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c0ca18ed396d4240ccad241ec4b02d
https://doi.org/10.1093/hmg/ddt283
https://doi.org/10.1093/hmg/ddt283
Autor:
Zhishuo Ou, Stephen Sanders, Jian Li, A. Craig Chinault, Edwin H. Cook, Chad A. Shaw, James S. Sutcliffe, Patrícia B. S. Celestino-Soper, Michael T. Murtha, Pawel Stankiewicz, Matthew W. State, Lea K. Davis, Susanne Thomson, Tomasz Gambin, A. Gulhan Ercan-Sencicek, Arthur L. Beaudet, Jennifer R. German, Aleksandar Milosavljevic
Publikováno v:
Human Molecular Genetics. 20:4360-4370
Autism is a neurodevelopmental disorder with increasing evidence of heterogeneous genetic etiology including de novo and inherited copy number variants (CNVs). We performed array comparative genomic hybridization using a custom Agilent 1 M oligonucle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77d3fe934a4b290fcbaa7aa004babeb2
https://doi.org/10.1093/hmg/ddr363
https://doi.org/10.1093/hmg/ddr363
Autor:
Sarika U. Peters, Marwan Shinawi, Craig Chinault, Trilochan Sahoo, Ankita Patel, Bruno Maranda, Arthur L. Beaudet, Cindy Skinner, Steve A. Skinner, Roger E. Stevenson, Roxanne R. Zascavage
Publikováno v:
American Journal of Medical Genetics Part A. 155:1272-1280
Genomic copy number imbalances are being increasingly identified as an important cause of intellectual disability and behavioral abnormalities. The typical deletion in WAGR syndrome encompasses the PAX6 and WT1 genes, but larger deletions have been a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f519ea4aff9cfa4dc13b930c3b929fc
https://doi.org/10.1002/ajmg.a.33878
https://doi.org/10.1002/ajmg.a.33878