Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Settara Chandrasekharappa"'
Autor:
Adebowale A. Adeyemo, Norann A. Zaghloul, Guanjie Chen, Ayo P. Doumatey, Carmen C. Leitch, Timothy L. Hostelley, Jessica E. Nesmith, Jie Zhou, Amy R. Bentley, Daniel Shriner, Olufemi Fasanmade, Godfrey Okafor, Benjamin Eghan, Kofi Agyenim-Boateng, Settara Chandrasekharappa, Jokotade Adeleye, William Balogun, Samuel Owusu, Albert Amoah, Joseph Acheampong, Thomas Johnson, Johnnie Oli, Clement Adebamowo, South Africa Zulu Type 2 Diabetes Case-Control Study, Francis Collins, Georgia Dunston, Charles N. Rotimi
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Type 2 diabetes (T2D) is prevalent in populations worldwide, however, mostly studied in European and mixed-ancestry populations. Here, the authors perform a genome-wide association study for T2D in over 5,000 sub-Saharan Africans and identify a locus
Externí odkaz:
https://doaj.org/article/7757796c1cc14b99b37e09335d62edfc
Autor:
Kendra A Williams, Minnkyong Lee, Ying Hu, Jonathan Andreas, Shashank J Patel, Suiyuan Zhang, Peter Chines, Abdel Elkahloun, Settara Chandrasekharappa, J Silvio Gutkind, Alfredo A Molinolo, Nigel P S Crawford
Publikováno v:
PLoS Genetics, Vol 10, Iss 11, p e1004809 (2014)
Although prostate cancer typically runs an indolent course, a subset of men develop aggressive, fatal forms of this disease. We hypothesize that germline variation modulates susceptibility to aggressive prostate cancer. The goal of this work is to id
Externí odkaz:
https://doaj.org/article/37dcb56c93a64c16bce461847a4a366a
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Supplementary Table 1 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ec8b76f839946d4975a4af5069edb12
https://doi.org/10.1158/0008-5472.22373850.v1
https://doi.org/10.1158/0008-5472.22373850.v1
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Supplementary Table 2 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::689cacbdd5675f70d677a6b9a4f5d6c1
https://doi.org/10.1158/0008-5472.22373847.v1
https://doi.org/10.1158/0008-5472.22373847.v1
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Supplementary Figure 1 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b9e96258c53418a227007e972323c4
https://doi.org/10.1158/0008-5472.22373859
https://doi.org/10.1158/0008-5472.22373859
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Genomic aberrations on chromosome 8 are common in colon cancer, and are associated with lymph node and distant metastases as well as with disease susceptibility. This prompted us to generate a high-resolution map of genomic imbalances of chromosome 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96d0e1880bf27ebdb5436a215a777f7c
https://doi.org/10.1158/0008-5472.c.6497229
https://doi.org/10.1158/0008-5472.c.6497229
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Supplementary Figure 2 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a0f9b938f93a9d2795ddeaf50be135
https://doi.org/10.1158/0008-5472.22373856.v1
https://doi.org/10.1158/0008-5472.22373856.v1
Autor:
Thomas Ried, B. Michael Ghadimi, Heinz Becker, Michael J. Difilippantonio, Yidong Chen, Settara Chandrasekharappa, Virginia Rodriguez, Amanda B. Hummon, Sandra Becker, Patrick Hörmann, Quang Tri Nguyen, Marian Grade, Jordi Camps
Supplementary Figure Legends 1-2 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b02bcd67355bec58e538dbe37a25bd2
https://doi.org/10.1158/0008-5472.22373853.v1
https://doi.org/10.1158/0008-5472.22373853.v1
Autor:
Kai Yu, Natalie Deuitch, Matthew Merguerian, Lea Cunningham, Joie Davis, Erica Bresciani, Jamie Diemer, Elizabeth Andrews, Alice Young, Frank Donovan, Raman Sood, Kathleen Craft, Shawn Chong, Settara Chandrasekharappa, Jim Mullikin, Paul P. Liu
Publikováno v:
bioRxiv
GermlineRUNX1mutations lead to familial platelet disorder with associated myeloid malignancies (FPDMM), which is characterized by thrombocytopenia and a life-long risk (35-45%) of hematological malignancies. We recently launched a longitudinal natura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d8cfc5ea8a6966780209e53b86a6eec
https://europepmc.org/articles/PMC9928034/
https://europepmc.org/articles/PMC9928034/
Autor:
Andrew L. Webster, Mathijs A. Sanders, Krupa Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach, Ryan R. White, Audrey M. Goldfarb, Kevin Hadi, Matthew M. Edwards, Frank X. Donovan, Moonjung Jung, Sunandini Sridhar, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer Kennedy, Lorenzo Bean, Rasim O. Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas Carrol, Eunike Velleuer, Jeff C. Rastatter, Susanne I. Wells, Jordi Surrallés, Grover Bagby, Margaret L. MacMillan, John E. Wagner, Maria Cancio, Farid Boulad, Theresa Scognamiglio, Roger Vaughan, Amnon Koren, Marcin Imielinski, Settara Chandrasekharappa, Arleen D. Auerbach, Bhuvanesh Singh, David Kutler, Peter J. Campbell, Agata Smogorzewska
Publikováno v:
Cancer Research. 82:6196-6196
Fanconi anemia (FA), a model syndrome of genome instability, is caused by a deficiency in DNA interstrand crosslink (ICL) repair resulting in chromosome breakage. The FA repair pathway comprises at least 22 FANC proteins including BRCA1 and BRCA2 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93046854d732003d6d22f0ca29e784e7
https://doi.org/10.1158/1538-7445.am2022-6196
https://doi.org/10.1158/1538-7445.am2022-6196