Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Vaithilingam G. Dev"'
Publikováno v:
Gene Reports. 25:101310
Objective To standardize simple PCR based technique to identify FLT3 mutations in patients with newly diagnosed acute myelogenous leukemia (AML). Material and methods Thirty six patients with different chromosomal presentation were included in the st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd5ba0bcf784189cd294cc089125749c
https://doi.org/10.1016/j.genrep.2021.101310
https://doi.org/10.1016/j.genrep.2021.101310
Autor:
Sarah Fuentes, Stephen Papa, Nagesh Rao, Daniel L. Van Dyke, Mingya Liu, Ernesto Fuentes, Navnit S. Mitter, Ramesh Babu, Prasad Koduru, Vaithilingam G. Dev
Publikováno v:
Archives of pathologylaboratory medicine. 142(2)
Context.— Chromosome analysis on bone marrow or peripheral blood samples fails in a small proportion of attempts. A method that is more reliable, with similar or better resolution, would be a welcome addition to the armamentarium of the cytogenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2421d435ffaaa5f837375601cd947b44
https://pubmed.ncbi.nlm.nih.gov/28981371
https://pubmed.ncbi.nlm.nih.gov/28981371
Autor:
Prasad Koduru, Ernesto Fuentes, Ramesh Babu, Cynthia M. Williamson, Srikanthi Kopuri, Vaithilingam G. Dev, Stephen Papa, Vandana Lal, Daniel L. Van Dyke, Mingya Liu, Minjae Kwon, Sarah Fuentes, Guangyu Gu, Saurabh Bhattacharya, Nagesh Rao
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Karyotype determination has a central role in the genetic workup of pregnancy loss, as aneuploidy (trisomy and monosomy) and polyploidy (triploidy and tetraploidy) are the cause in at least 50% of first trimester, 25% of second trimester,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f18fe0108dd5f5431c6a8dc2a727c9
https://pubmed.ncbi.nlm.nih.gov/29573570
https://pubmed.ncbi.nlm.nih.gov/29573570
Autor:
Cynthia M. Williamson, Stephen Papa, Vaithilingam G. Dev, Peter Papenhausen, Daniel L. Van Dyke, Sarah Fuentes, Ramesh Babu, Mingya Liu, Stuart Schwartz, Prasad Koduru, Srikanthi Kopuri, Jim Tepperberg, Ernesto Fuentes
Publikováno v:
Cancer Genetics. :61-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d983e71c230240a04dc90142b259701a
https://doi.org/10.1016/j.cancergen.2018.04.032
https://doi.org/10.1016/j.cancergen.2018.04.032
Publikováno v:
Leukemia Research. 33:e98-e103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd7062e53fff0bc7e9554fd02dce2f32
https://doi.org/10.1016/j.leukres.2009.01.038
https://doi.org/10.1016/j.leukres.2009.01.038
Publikováno v:
Cancer Genetics. 209:242-243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11ba230af9bb669a563fd65e9eb8c69f
https://doi.org/10.1016/j.cancergen.2016.05.044
https://doi.org/10.1016/j.cancergen.2016.05.044
Publikováno v:
Ophthalmic Paediatrics and Genetics. 6:7-15
Abnormal centromere-chromatid apposition (ACCA) was noted in a patient with Peters' anomaly. Previous reports of ACCA emphasized its association with tetraphocomelia and other congenital malformations (Roberts, SC Phocomelia, Pseudothalidomide Syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d61fe03614ff97a1e64d539e081214d
https://doi.org/10.3109/13816818509004111
https://doi.org/10.3109/13816818509004111
Autor:
Andrew J. Carroll, Vaithilingam G. Dev, William M. Crist, Vipul N. Mankad, Raymond D.A. Peterson
Publikováno v:
Cancer Genetics and Cytogenetics. 10:205-208
A 13-month-old female with middle and upper lobe pneumonia showed a high WBC count with 99% blasts. From hematologic studies the condition was diagnosed as acute myelocytic leukemia (AML). In spite of aggressive chemotherapy, the patient died. Unstim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cfc657746ec259ecd9bf4cac6c5a431
https://doi.org/10.1016/0165-4608(83)90126-7
https://doi.org/10.1016/0165-4608(83)90126-7
Autor:
Orlando J. Miller, Ramana V. Tantravahi, Vaithilingam G. Dev, Dorothy A. Miller, Carlo M. Croce
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 73(12)
Most mouse-human somatic cell hybrids show preferential loss of human chromosomes, absence of human 28S ribosomal RNA, and suppression of human nucleolus organizer activity, as visualized by the Ag-AS silver histochemical stain. In contrast, the mous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e160dcd70cd076fbb8629b6832a6a334
https://pubmed.ncbi.nlm.nih.gov/1070003
https://pubmed.ncbi.nlm.nih.gov/1070003
Autor:
Merlin G. Butler, Vaithilingam G. Dev, Dinesh Shah, Janet E. Ulm, Patrick L. Wilmot, Lawrence R. Shapiro, John M. Opitz, James F. Reynolds
Publikováno v:
American journal of medical genetics. 31(4)
Early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal diagnosis were undertaken for the first time in a 17-week gestation fetus at risk for the fragile X [fra (X)] syndrome. Metaphase spreads from 300 fetal ly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23097fd9b40fe44efdd8ba5caaf572e0
https://pubmed.ncbi.nlm.nih.gov/3239566
https://pubmed.ncbi.nlm.nih.gov/3239566