Zobrazeno 1 - 10
of 15
pro vyhledávání: '"James M. Fink"'
Autor:
Ashwini K. Yenamandra, Rebecca B. Smith, T. Niroshi Senaratne, Sung-Hae L Kang, James M. Fink, Gregory Corboy, Casey A Hodge, Xinyan Lu, Susan Mathew, Susan Crocker, Min Fang
Publikováno v:
Cancer Genetics. :1-21
Diffuse large B cell lymphoma, not otherwise specified (DLBCL, NOS) is the most common type of non-Hodgkin lymphoma (NHL). The 2016 World Health Organization (WHO) classification defined DLBCL, NOS and its subtypes based on clinical findings, morphol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::235d43b3237a81f59023d9b8c185a0d6
https://doi.org/10.1016/j.cancergen.2022.07.006
https://doi.org/10.1016/j.cancergen.2022.07.006
Autor:
Shaji Kumar, Rhett P. Ketterling, Jess F. Peterson, James M. Fink, Linda B. Baughn, Kathryn E. Pearce, Ross A. Rowsey, Patricia T. Greipp, Cherisse A. Marcou, Kaaren K. Reichard, Daniel L. Van Dyke, Mei Yin C. Polley, Lori Frederick, Cynthia M. Williamson, David S. Viswanatha
Publikováno v:
Blood Cancer Journal
Blood Cancer Journal, Vol 9, Iss 3, Pp 1-6 (2019)
Blood Cancer Journal, Vol 9, Iss 3, Pp 1-6 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2d869c5942c216ec81cffb0b477086
http://europepmc.org/articles/PMC6381150
http://europepmc.org/articles/PMC6381150
Autor:
Ashwini Yenamandra, Pascale Willem, James M. Fink, Rebecca B. Smith, Susan Crocker, Rashmi Kanagal Shamana, Greg Corboy, Min Fang, Sarah Rapisardo, Kilannin Krysiak, Susan Mathew, Anna Hodge, Debra Saxe, Mary Haddadin
Publikováno v:
Cancer Genetics. 244:26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::727c31ccf5c67e9d5df1f7705df96a32
https://doi.org/10.1016/j.cancergen.2020.04.073
https://doi.org/10.1016/j.cancergen.2020.04.073
Autor:
James M. Fink, Min Fang, Joyce Murata-Collins, Susan Mathew, Pascale Willem, Trevor J. Pugh, Xinyan Lu
Publikováno v:
Cancer genetics.
Background Plasma cell neoplasms (PCNs) encompass a spectrum of disorders including monoclonal gammopathy of undetermined significance, smoldering myeloma, plasma cell myeloma, and plasma cell leukemia. Molecular subtypes have been defined by recurre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f69a4a43cac9fb87e0a2c93166a07f89
https://pubmed.ncbi.nlm.nih.gov/30393007
https://pubmed.ncbi.nlm.nih.gov/30393007
Publikováno v:
ISRN Pediatrics
Chromosome 22q13.3 deletion syndrome is a well-recognized cause of global developmental delay, while duplication of the same chromosome is a rare occurrence. The presence of both abnormalities in the same family has never been reported, to our knowle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f70082d49bdb63c2c5dd05a9017c887f
https://doi.org/10.5402/2011/829825
https://doi.org/10.5402/2011/829825
Publikováno v:
American Journal of Medical Genetics. :398-402
Patients with trisomies or duplications of distal 15q have rarely been reported in the literature. Previous authors [Zollino et al., 1999: Am J Med Genet 87:391-394] have described a distal 15q trisomy syndrome, including the unusual features of pren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c9bbea2114497adcec425afb08692bb
https://doi.org/10.1002/ajmg.a.20617
https://doi.org/10.1002/ajmg.a.20617
Autor:
Sophia Yohe, Katherine Park, Virginia Kubic, Robert W. McKenna, Michael A. Linden, James M. Fink, Vanessa J. Dayton
Publikováno v:
Archives of pathologylaboratory medicine. 138(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::188c2de8ee3b48b3fa2b470215beae17
https://pubmed.ncbi.nlm.nih.gov/26125423
https://pubmed.ncbi.nlm.nih.gov/26125423
Publikováno v:
American Journal of Medical Genetics. 101:50-54
We report a 3-year-old girl with trisomy 2p24.3-pter who presented with marked psychomotor delay and dysmorphic features. This patient represents the only known case of trisomy 2p24.3-2pter that does not involve an associated functional monosomy. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f04c5aa25eb852906233cada07b4df5d
https://doi.org/10.1002/ajmg.1309
https://doi.org/10.1002/ajmg.1309
Autor:
Janet S. Payne, Ardis Sophian, Susan Arnold, B. Rafael Elejalde, Leslie A. Willis, Ann Wiktor, Wei-Tong Hsu, Gerald A. Hoeltge, Eric B. Johnson, Rodney R. Higgins, LeAnn Oseth, Susan Sheldon, Lorraine F. Meisner, James M. Fink, Peter Van Tuinen, Gordon W. Dewald, Julie Zenger-Hain, Jar-Fee Yung, Gail D. Wenger, Stuart Schwartz, Patrick D. Storto, Mark A. Micale, Richard Stallard, Tina M. Ceperich, A. Alsaadi, Ruthann I. Blough, D. James McCorquodale, Diane L Kronberger, Higgins Jv
Publikováno v:
Cancer Genetics and Cytogenetics. 116:97-104
Twenty-eight laboratories evaluated a new fluorescence in situ hybridization (FISH) strategy for chronic myeloid leukemia. In a three-part study, bcr/abl1 D-FISH probes were used to study bone marrow specimens. First, laboratories familiarized themse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b6cae9416f89cfa7ca7b524ae5ee0d7
https://doi.org/10.1016/s0165-4608(99)00120-x
https://doi.org/10.1016/s0165-4608(99)00120-x
Publikováno v:
Journal of gastroenterology. 42(3)
Genetic instability is a hallmark of malignancy, and microsatellite instability is a widely appreciated mechanism of generating genetic changes. We have recently observed four markers clustered on chromosome 20 that showed the effects of microsatelli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0378ab801740bb33d0963a86c907f6cd
https://pubmed.ncbi.nlm.nih.gov/17380277
https://pubmed.ncbi.nlm.nih.gov/17380277