Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Grover, Bagby"'
Autor:
Andrew L. H. Webster, Mathijs A. Sanders, Krupa Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach, Ryan R. White, Audrey Goldfarb, Kevin Hadi, Matthew M. Edwards, Frank X. Donovan, Remco M. Hoogenboezem, Moonjung Jung, Sunandini Sridhar, Tom F. Wiley, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer A. Kennedy, Lorenzo Bean, Rasim O. Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas S. Carroll, Sanjana Shroff, Michael Beaumont, 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, Kristin G. Beaumont, Amnon Koren, Marcin Imielinski, Settara C. Chandrasekharappa, Arleen D. Auerbach, Bhuvanesh Singh, David I. Kutler, Peter J. Campbell, Agata Smogorzewska
Publikováno v:
Nature, 612(7940), 495-502. Nature Publishing Group
Nature
Nature
Fanconi anaemia (FA), a model syndrome of genome instability, is caused by a deficiency in DNA interstrand crosslink repair resulting in chromosome breakage1–3. The FA repair pathway protects against endogenous and exogenous carcinogenic aldehydes4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15cd1011ef44b739a461beaa02a1cb6
https://doi.org/10.1038/s41586-022-05253-4
https://doi.org/10.1038/s41586-022-05253-4
Autor:
Grover Bagby
Publikováno v:
F1000Research, Vol 7 (2018)
Fanconi anemia is an inherited disease characterized by genomic instability, hypersensitivity to DNA cross-linking agents, bone marrow failure, short stature, skeletal abnormalities, and a high relative risk of myeloid leukemia and epithelial maligna
Externí odkaz:
https://doaj.org/article/25f4a8eb8b9d491fa6cbbe8f79ea1429
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
Autor:
Kevin P. Battaile, Raynard L. Bateman, Derik Mortimer, Jean Mulcahy, R. Keaney Rathbun, Grover Bagby, William H. Fleming, Markus Grompe
Publikováno v:
Blood. 94:2151-2158
Fanconi anemia (FA) is an autosomal recessive disorder characterized by birth defects, increased incidence of malignancy, and progressive bone marrow failure. Bone marrow transplantation is therapeutic and, therefore, FA is a candidate disease for he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c52ed3667a361d2d8f994759871c9adf
https://doi.org/10.1182/blood.v94.6.2151.418a22_2151_2158
https://doi.org/10.1182/blood.v94.6.2151.418a22_2151_2158
Autor:
Meenakshi, Noll, Kevin P, Battaile, Raynard, Bateman, Timothy P, Lax, Keany, Rathbun, Carol, Reifsteck, Grover, Bagby, Milton, Finegold, Susan, Olson, Markus, Grompe
Publikováno v:
Experimental hematology. 30(7)
Fanconi anemia (FA) is a genetically heterogeneous disorder associated with defects in at least eight genes. The biochemical function(s) of the FA proteins are unknown, but together they define the FA pathway, which is involved in cellular responses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::98bb035aa076c7969424a8e71d46303b
https://pubmed.ncbi.nlm.nih.gov/12135664
https://pubmed.ncbi.nlm.nih.gov/12135664
Autor:
Grover Bagby
Publikováno v:
Aplastic Anemia and Other Bone Marrow Failure Syndromes ISBN: 9781461279358
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e195d6ef054ff8c1ee402d5b15b4881f
https://doi.org/10.1007/978-1-4612-3254-4_17
https://doi.org/10.1007/978-1-4612-3254-4_17
Autor:
Grover Bagby
Publikováno v:
Revista Iberoamericana. 37:461-464
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84730817d128c682c6fb64767b06739e
https://doi.org/10.5195/reviberoamer.1971.2695
https://doi.org/10.5195/reviberoamer.1971.2695