Torthaí cuardaigh - Rachid Karam
- 1 - 20 toradh as 24 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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1
Regulation of nonsense-mediated mRNA decay: Implications for physiology and disease de réir Rachid Karam, Jordan Wengrod, Lawrence B. Gardner, Miles Wilkinson
Foilsithe / Cruthaithe 2013Artigo -
2
Saturation-scale functional evidence supports clinical variant interpretation in Lynch syndrome de réir Anthony Scott, Felicia Hernandez, Adam Chamberlin, Cathy Smith, Rachid Karam, Jacob O. Kitzman
Foilsithe / Cruthaithe 2022Artigo -
3
The unfolded protein response is shaped by the <scp>NMD</scp> pathway de réir Rachid Karam, Chih‐Hong Lou, Heike Kroeger, Lulu Huang, Jonathan H. Lin, Miles Wilkinson
Foilsithe / Cruthaithe 2015Artigo -
4
Genetics of gastric cancer: what do we know about the genetic risks? de réir Thomas P. Slavin, Jeffrey N. Weitzel, Susan L. Neuhausen, Kasmintan A. Schrader, Carla Oliveíra, Rachid Karam
Foilsithe / Cruthaithe 2019Revisão -
5
Posttranscriptional Control of the Stem Cell and Neurogenic Programs by the Nonsense-Mediated RNA Decay Pathway de réir Chih H. Lou, Ada Shao, Eleen Y. Shum, Josh L. Espinoza, Lulu Huang, Rachid Karam, Miles Wilkinson
Foilsithe / Cruthaithe 2014Artigo -
6
Beyond DNA: An Integrated and Functional Approach for Classifying Germline Variants in Breast Cancer Genes de réir Tina Pesaran, Rachid Karam, Robert Huether, S. Li, Suzette Farber-Katz, Adam Chamberlin, Hansook Kim Chong, Holly LaDuca, Aaron Elliott
Foilsithe / Cruthaithe 2016Revisão -
7
RNA Homeostasis Governed by Cell Type-Specific and Branched Feedback Loops Acting on NMD de réir Lulu Huang, Chih-Hong Lou, Waikin Chan, Eleen Y. Shum, Ada Shao, Erica L. Stone, Rachid Karam, Hye-Won Song, Miles Wilkinson
Foilsithe / Cruthaithe 2011Artigo -
8
Clinical features and cancer risk in families with pathogenic<i>CDH1</i>variants irrespective of clinical criteria de réir Rosa M. Xicola, Shuwei Li, Nicolette J. Rodriguez, Patrick Reinecke, Rachid Karam, Virginia Speare, Mary Helen Black, Holly LaDuca, Xavier Llor
Foilsithe / Cruthaithe 2019Artigo -
9
Identification of a MicroRNA that Activates Gene Expression by Repressing Nonsense-Mediated RNA Decay de réir Ivone G. Bruno, Rachid Karam, Lulu Huang, Anjana Bhardwaj, Chih H. Lou, Eleen Y. Shum, Hye-Won Song, Mark Corbett, Wesley D. Gifford, Jozef Gécz, Samuel L. Pfaff, Miles Wilkinson
Foilsithe / Cruthaithe 2011Artigo -
10
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN de réir Shawn Fayer, Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick, Felicia Hernandez, Tina Pesaran, Rachid Karam, Brian H. Shirts, Douglas M. Fowler, Lea M. Starita
Foilsithe / Cruthaithe 2021Artigo -
11
Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing de réir Carolyn Horton, Lily Hoang, Heather Zimmermann, Colin C. Young, Jessica Grzybowski, Kate Durda, Huy Gia Vuong, David Burks, Ashley Cass, Holly LaDuca, Marcy E. Richardson, Steven M. Harrison, Elizabeth Chao, Rachid Karam
Foilsithe / Cruthaithe 2023Artigo -
12
Quantification of Epigenetic and Genetic 2nd Hits in CDH1 During Hereditary Diffuse Gastric Cancer Syndrome Progression de réir Carla Oliveíra, Sónia Sousa, Hugo Pinheiro, Rachid Karam, Renata Bordeira–Carriço, Janine Senz, Pardeep Kaurah, Joana Carvalho, Rui Pereira, Leonor Gusmão, Xiaogang Wen, Maria Augusta Cipriano, Jun Yokota, Fátima Carneiro, David G. Huntsman, Raquel Seruca
Foilsithe / Cruthaithe 2009Artigo -
13
Gene‐specific criteria for <i>PTEN</i> variant curation: Recommendations from the ClinGen PTEN Expert Panel de réir Jessica L. Mester, Rajarshi Ghosh, Tina Pesaran, Robert Huether, Rachid Karam, Kathleen S. Hruska, Helio A. Costa, Katherine Lachlan, Joanne Ngeow, Jill S. Barnholtz‐Sloan, Kaitlin Sesock, Felicia Hernandez, Liying Zhang, Laura V. Milko, Sharon E. Plon, Madhuri Hegde, Charis Eng
Foilsithe / Cruthaithe 2018Artigo -
14
The UPF1 RNA surveillance gene is commonly mutated in pancreatic adenosquamous carcinoma de réir Chen Liu, Rachid Karam, Yingqi Zhou, Fang Su, Yuan Ji, Gang Li, Guo‐Tong Xu, Lixia Lü, Chongren Wang, Meiyi Song, Jingping Zhu, Yiran Wang, Yifan Zhao, Wai Chin Foo, Mingxin Zuo, Mark A. Valasek, Milind Javle, Miles Wilkinson, Yanjun Lu
Foilsithe / Cruthaithe 2014Artigo -
15
Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer de réir Rachid Karam, Blair R. Conner, Holly LaDuca, Kelly McGoldrick, Kate Krempely, Marcy E. Richardson, Heather Zimmermann, Stephanie Gutierrez, Patrick Reineke, Lily Hoang, Kyle Allen, Amal Yussuf, Suzette Farber-Katz, Huma Q. Rana, Samantha Culver, John Lee, Sarah Nashed, Deborah Toppmeyer, Debra L. Collins, Ginger Haynes, Tina Pesaran, Jill S. Dolinsky, Brigette Tippin Davis, Aaron Elliott, Elizabeth Chao
Foilsithe / Cruthaithe 2019Artigo -
16
Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer de réir Thierry Frébourg, Carla Oliveíra, Patrick Hochain, Rachid Karam, Sylvie Manouvrier, Carla Graziadio, Michel Vekemans, A Hartmann, Stéphanie Baert‐Desurmont, C Alexandre, S Lejeune Dumoulin, Cláudio Augusto Marroni, Cosette Martin, Sérgio Castedo, Michael Lovett, Janet S. Winston, José Carlos Machado, Tania Attié‐Bitach, Ethylin Wang Jabs, Juanliang Cai, P. Pellerin, J.-P. Triboulet, Michel Scotté, Florence Le Pessot, A Hedouin, Fátima Carneiro, Martine Blayau, Raquel Seruca
Foilsithe / Cruthaithe 2005Artigo -
17
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>CDH1</i> sequence variants de réir Kristy Lee, Kate Krempely, Maegan E. Roberts, Michael J. Anderson, Fátima Carneiro, Elizabeth Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David G. Huntsman, Pardeep Kaurah, Chimene Kesserwan, Tyler Landrith, Shuwei Li, Arjen R. Mensenkamp, Carla Oliveíra, Carolina Pardo‐Díaz, Tina Pesaran, Matthew Richardson, Thomas P. Slavin, Amanda B. Spurdle, Mackenzie Trapp, Leora Witkowski, Charles Sunghoon Yi, Liying Zhang, Sharon E. Plon, Kasmintan A. Schrader, Rachid Karam
Foilsithe / Cruthaithe 2018Artigo -
18
Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain de réir Chunling Hu, Huaizhi Huang, Jie Na, Carolyn A. Lumby, Mohamed Abozaid, Megan Holdren, T. Jagan Mohan Rao, Rachid Karam, Tina Pesaran, Jamie Weyandt, Christen M. Csuy, Christina Seelaus, Colin C. Young, Kelly Fulk, Zahra Heidari, Paulo C. Lyra, Ronan E. Couch, Benjamin Persons, Eric C. Polley, Rohan Gnanaolivu, Nicholas J. Boddicker, Álvaro N.A. Monteiro, Siddhartha Yadav, Susan M. Domchek, Marcy E. Richardson, Fergus J. Couch
Foilsithe / Cruthaithe 2024Artigo -
19
Targeting cellular heterogeneity with CXCR2 blockade for the treatment of therapy-resistant prostate cancer de réir Yanjing Li, Yiping He, William Butler, Lingfan Xu, Yan Chang, Kefeng Lei, Hong Zhang, Yinglu Zhou, Allen C. Gao, Qingfu Zhang, Daniel Taylor, Donghui Cheng, Suzette Farber-Katz, Rachid Karam, Tyler Landrith, Bing Li, Sitao Wu, Vickie Hsuan, Qing Yang, Hailiang Hu, Xufeng Chen, Melissa Flowers, Shannon J. McCall, John K. Lee, B. Smith, Jung Wook Park, Andrew S. Goldstein, Owen N. Witte, Qianben Wang, Matthew B. Rettig, Andrew J. Armstrong, Qing Cheng, Jiaoti Huang
Foilsithe / Cruthaithe 2019Artigo -
20
Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup de réir Logan C. Walker, Miguel de la Hoya, George A. R. Wiggins, Amanda Lindy, Lisa M. Vincent, Michael T. Parsons, Daffodil M. Canson, Dana M. Bis‐Brewer, Ashley Cass, Alexander Tchourbanov, Heather Zimmermann, Alicia B. Byrne, Tina Pesaran, Rachid Karam, Steven M. Harrison, Amanda B. Spurdle, Leslie G. Biesecker, Steven M. Harrison, Ahmad Abou Tayoun, Jonathan S. Berg, Steven E. Brenner, Garry R. Cutting, Sian Ellard, Marc S. Greenblatt, Peter B. Kang, Izabela Karbassi, Rachel Karchin, Jessica L. Mester, Anne O’Donnell‐Luria, Tina Pesaran, Sharon E. Plon, Heidi L. Rehm, Natasha T. Strande, Sean V. Tavtigian, Scott Topper
Foilsithe / Cruthaithe 2023Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Gene
Cancer
Medicine
Bioinformatics
Computational biology
Mutation
Genetic testing
Germline
Internal medicine
RNA
Cell
RNA splicing
Cell biology
Germline mutation
Nonsense-mediated decay
Oncology
Phenotype
CDH1
Cadherin
Cancer research
Colorectal cancer
DNA mismatch repair
Exon
Missense mutation
Pathology
microRNA
Alternative splicing
Apoptosis