Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Shashirekha, Shetty"'
Autor:
Qianze Dong, Tarneem Darwish, Meyerson Howard, Shashirekha Shetty, Yang Wang, Yan Xiu, Molly Gallogly, Chen Zhao
Publikováno v:
Journal of International Medical Research, Vol 52 (2024)
Philadelphia chromosome-positive (Ph+) T-cell acute lymphoblastic leukemia (T-ALL) is a rare and aggressive type of acute leukemia. The Philadelphia chromosome is the hallmark of chronic myeloid leukemia (CML). The differentiation between Ph+ T-ALL a
Externí odkaz:
https://doaj.org/article/cfa364fd4a164cd694c4d22734c32500
Autor:
Emily Spector, Erica Andersen, John Herriges, Anne Higgins, Brynn Levy, Ludmila Matyakhina, Christa Martin, Daniel Pineda-Alvarez, Lina Shao, Shashirekha Shetty, Andrea Vaags, Erik Thorland, Sung-Hae Kang, Chelsea Lowther, Dominic McMullan, Erin Riggs
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101482- (2024)
Externí odkaz:
https://doaj.org/article/6b825c0959e04ded8ace392a65ab52d6
Autor:
Joshua L. Deignan, Vimla Aggarwal, Allen E. Bale, Daniel B. Bellissimo, Jessica K. Booker, Yang Cao, Kristy R. Crooks, Kristen L. Deak, Daniela Del Gaudio, Birgit Funke, Nicole L. Hoppman, Vanessa Horner, Robert B. Hufnagel, Colleen Jackson-Cook, Prasad Koduru, Marco L. Leung, Shibo Li, Pengfei Liu, Minjie Luo, Rong Mao, Heather Mason-Suares, Fady M. Mikhail, Stephen R. Moore, Rizwan C. Naeem, Laura M. Pollard, Elena A. Repnikova, Lina Shao, Brandon M. Shaw, Shashirekha Shetty, Teresa A. Smolarek, Elizabeth Spiteri, Jessica Van Ziffle, Gail H. Vance, Cindy L. Vnencak-Jones, Eli S. Williams
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101820- (2024)
Purpose: The specialty of Laboratory Genetics and Genomics (LGG) was created in 2017 in an effort to reflect the increasing convergence in technologies and approaches between clinical molecular genetics and clinical cytogenetics. However, there has n
Externí odkaz:
https://doaj.org/article/06de2e3b5f9244b89cae6954ab35c034
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Human prion diseases are rapidly progressive and fatal neurodegenerative conditions caused by a disease-causing isoform of the native prion protein. The prion protein gene (PRNP) encodes for the cellular prion protein, which is the biological substra
Externí odkaz:
https://doaj.org/article/44f5d1173322450ba374171242e3e64b
Autor:
Catherine K. Gestrich, Shanelle J. De Lancy, Adam Kresak, Mohamad G. Sinno, Akua Yalley, Irina Pateva, Howard Meyerson, Shashirekha Shetty, Kwadwo A. Oduro
Publikováno v:
Human Pathology. 136:75-83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98edb9f0174c9370215bf4aa0f2b0884
https://doi.org/10.1016/j.humpath.2023.03.018
https://doi.org/10.1016/j.humpath.2023.03.018
A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques
Autor:
Rabeah Bayazid, Christina Orru’, Rabail Aslam, Yvonne Cohen, Amelia Silva-Rohwer, Seong-Ki Lee, Rossana Occhipinti, Qingzhong Kong, Shashirekha Shetty, Mark L. Cohen, Byron Caughey, Lawrence B. Schonberger, Brian S. Appleby, Ignazio Cali
Publikováno v:
Acta Neuropathologica.
The presence of amyloid kuru plaques is a pathological hallmark of sporadic Creutzfeldt–Jakob disease (sCJD) of the MV2K subtype. Recently, PrP plaques (p) have been described in the white matter of a small group of CJD (p-CJD) cases with the 129MM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abdccc88e9ea950414a8db03ef007dcb
https://doi.org/10.1007/s00401-023-02581-1
https://doi.org/10.1007/s00401-023-02581-1
Publikováno v:
International Journal of Surgical Pathology. :106689692311683
Lymphoplasmacytic lymphoma often needs to be differentiated from other B-cell lymphomas with plasmacytic differentiation, especially marginal zone cell lymphoma. Molecular detection of MYD88 p.L265P hotspot mutation supports the diagnosis of lymphopl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79e0af71d6ae57b4c51313185b060f6b
https://doi.org/10.1177/10668969231168359
https://doi.org/10.1177/10668969231168359
Autor:
Audrey N, Jajosky, Anna L, Mitchell, Mahmut, Akgul, Shashirekha, Shetty, Jennifer M, Yoest, Stanton L, Gerson, Navid, Sadri, Kwadwo A, Oduro
Publikováno v:
Genes. 13(4)
Germline disruptive variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33a2de1e293277d16ad000202638fe30
https://pubmed.ncbi.nlm.nih.gov/35456397
https://pubmed.ncbi.nlm.nih.gov/35456397
Autor:
Nikhil A Sangle, Rong Mao, Shashirekha Shetty, Joshua D Schiffman, Christopher Dechet, Lester Layfield, Neeraj Agarwal, Ting Liu
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 56, Iss 4, Pp 428-433 (2013)
Tubulocystic renal cell carcinoma (TRCC) is an indolent type of renal cell carcinoma with a good prognosis based on the limited number of published cases. Herein, we describe the unusual clinical, pathologic and molecular findings in a case of TRCC.
Externí odkaz:
https://doaj.org/article/985ab8b7a78648d6aa657d8530a58273
Autor:
Melissa Keinath, Ignazio Cali, Megan Piazza, Mark Cohen, Curtis Tatsuoka, Thomas Prior, Brian Appleby, Shashirekha Shetty
Publikováno v:
Genetics in Medicine. 24:S230-S231
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d226fdd1fa1e3e06f205be875dd66a2
https://doi.org/10.1016/j.gim.2022.01.401
https://doi.org/10.1016/j.gim.2022.01.401