Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Rizwan, Naeem"'
Autor:
Abul Kalam Azad, Lindsay Yanakakis, Samantha Issleb, Jessica Turina, Kelli Drabik, Christina Bonner, Eve Simi, Andrew Wagner, Morry Fiddler, Rizwan Naeem
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Full or partial monosomy of chromosome (chr) 21 is a very rare abnormal cytogenetic finding. It is characterized by variable sizes and deletion breakpoints on the long arm (q) of chr 21 that lead to a broad spectrum of phenotypes
Externí odkaz:
https://doaj.org/article/8ad9111576624b69945fa87b8f5f5c34
Supplementary Methods, Figures 1-6, Table 1 from Overexpression of Eg5 Causes Genomic Instability and Tumor Formation in Mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7fa22149f9c531cdc74a1ef40793c2
https://doi.org/10.1158/0008-5472.22371011.v1
https://doi.org/10.1158/0008-5472.22371011.v1
Proper chromosome segregation in eukaryotes is driven by a complex superstructure called the mitotic spindle. Assembly, maintenance, and function of the spindle depend on centrosome migration, organization of microtubule arrays, and force generation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a5a97746f7126af84a18f5141e44896
https://doi.org/10.1158/0008-5472.c.6496637
https://doi.org/10.1158/0008-5472.c.6496637
Autor:
Richard L. Haspel, Jonathan R. Genzen, Jay Wagner, Karen Fong, Rebecca Wilcox, Patricia V. Adem, Hana Anderson, James B. Atkinson, Leah W. Burke, Loren Joseph, Robin D. LeGallo, Madelyn Lew, Christina M. Lockwood, Rizwan Naeem, Hasan Rizvi, Julian Sanz Ortega, Kate Shane-Carson, Mark E. Sobel, Eric Suarez, Laura J. Tafe, Jason Wang, Rebecca L. Wilcox
Publikováno v:
Genetics in Medicine. 23:1151-1157
Purpose To assess, from the student perspective, medical school training in genetics and genomics. Methods In 2019, the Undergraduate Training in Genomics (UTRIG) Working Group developed genetics-related survey and knowledge questions for the RISE-FI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a957ed3bb096446b5548bd9f10550137
https://doi.org/10.1038/s41436-021-01100-5
https://doi.org/10.1038/s41436-021-01100-5
Publikováno v:
International Journal of Laboratory Hematology. 43:651-657
Introduction Adult T-Cell Leukemia/Lymphoma (ATLL) is an aggressive T-cell malignancy without known characteristic cytogenetic abnormalities. Recurrent mutations in TP53, APC, and epigenetic and histone-modifying genes have been identified in North A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30237206c22803500aea64f2364a52ca
https://doi.org/10.1111/ijlh.13577
https://doi.org/10.1111/ijlh.13577
Autor:
Myla Ashfaq, Syed A. Ahmed, Rabia Aziz-Rizvi, Zahra Hasan, Salman Kirmani, Shama Munim, Rizwan Naeem, Jamal Raza, Aisha Furqan
Publikováno v:
Journal of community genetics.
While the prevalence of genetic disorders has been well documented in the Muslim-majority, low-socioeconomic country of Pakistan, the provision of medical genetic services remains limited and cost-prohibitive to the masses in the country. With the ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db4c0e70214b9a71af53b37a42e73bd8
https://pubmed.ncbi.nlm.nih.gov/36264421
https://pubmed.ncbi.nlm.nih.gov/36264421
Autor:
Sebastian A. Jofre, Maxwell Roth, Arash H. Lahouti, Adam Gersten, Abul Kalam Azad, Robert D. Kelsch, Saeed Asiry, Yitzchak Goldstein, Rizwan Naeem, Rema Rao
Publikováno v:
Diagnostic cytopathologyREFERENCES. 50(6)
Ameloblastomas are benign but locally aggressive odontogenic tumors that commonly present as expansile lesions in the tooth-bearing areas. Fine-needle aspiration (FNA) biopsies of ameloblastomas are rare in clinical practice, and only a handful of ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f81fde41956c67306ac379c5d1c2d53b
https://pubmed.ncbi.nlm.nih.gov/35077030
https://pubmed.ncbi.nlm.nih.gov/35077030
Autor:
Myla Ashfaq, Syed Ajaz Ahmed, Rabia Aziz-Rizvi, Zahra Hasan, Salman Kirmani, Shama Munim, Rizwan Naeem, Jamal Raza, Aisha Furqan
Publikováno v:
Genetics in Medicine. 24:S304-S305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138a7f991e3e0b6755353e5be805cf39
https://doi.org/10.1016/j.gim.2022.01.510
https://doi.org/10.1016/j.gim.2022.01.510
Autor:
Hongwei Zou, Chih Kang Huang, Abul Kalam Azad, Hong Jin, Y. Goldstein, Rizwan Naeem, Juan Du, Morry Fiddler, Lindsay Yanakakis
Publikováno v:
Laboratory Medicine. 51:408-415
Background Individuals whose copies of the survival motor neuron 1 (SMN1) gene exist on the same chromosome are considered silent carriers for spinal muscular atrophy (SMA). Conventional screening for SMA only determines SMN1 copy number without any
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99b3903570c906c3e1910cc4af9fb1d7
https://doi.org/10.1093/labmed/lmz088
https://doi.org/10.1093/labmed/lmz088
Publikováno v:
American Journal of Clinical Pathology. 156:S9-S10
Introduction Genetic testing has become ubiquitous in clinical medicine and plays an important role in making diagnoses and guiding treatment plans. Indiscriminate use of these tests can cause duplicate testing, which is typically not indicated becau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f610b2ab689d8df2de9db7ffe81908d9
https://doi.org/10.1093/ajcp/aqab189.016
https://doi.org/10.1093/ajcp/aqab189.016