Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Cinthya Zepeda Mendoza"'
Autor:
Megan Lyon, Deborah Maiese, Rhonda West, Marci Sontag, Vivian Pan, Cinthya Zepeda Mendoza, Joann Bodurtha
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101398- (2024)
Externí odkaz:
https://doaj.org/article/17991cadf73f4107ad18c14f6f983b55
Autor:
Timothy Tidwell, Anthony Gregg, Wayne Grody, Michael Guo, Hutton Kearney, Kristin Monaghan, Jennifer Taylor, Cinthya Zepeda Mendoza, Catherine Ziats, Joshua Deignan, Karen Raraigh
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101576- (2024)
Externí odkaz:
https://doaj.org/article/2bc1c6aac3e3417c8ddb5e2f21d07dc0
Autor:
Beth A. Pitel, Cinthya Zepeda-Mendoza, Zohar Sachs, Hongwei Tang, Suganti Shivaram, Neeraj Sharma, James B. Smadbeck, Stephanie A. Smoley, Kathryn E. Pearce, Ivy M. Luoma, Joselle Cook, Mark R. Litzow, Nicole L. Hoppman, David Viswanatha, Xinjie Xu, Rhett P. Ketterling, Patricia T. Greipp, Jess F. Peterson, Linda B. Baughn
Publikováno v:
Blood Cancer Journal, Vol 13, Iss 1, Pp 1-5 (2023)
Externí odkaz:
https://doaj.org/article/aeebb67adf5c4359bd02b1d433a4766a
Autor:
Beth A. Pitel, Neeraj Sharma, Cinthya Zepeda-Mendoza, James B. Smadbeck, Kathryn E. Pearce, Joselle M. Cook, George Vasmatzis, Zohar Sachs, Rashmi Kanagal-Shamanna, David Viswanatha, Sheng Xiao, Robert B. Jenkins, Xinjie Xu, Nicole L. Hoppman, Rhett P. Ketterling, Jess F. Peterson, Patricia T. Greipp, Linda B. Baughn
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 2, Pp 1-4 (2021)
Externí odkaz:
https://doaj.org/article/025690d4be014f22ba7775cfae5b9a03
Autor:
Cinthya Zepeda‐Mendoza, McKinsey L. Goodenberger, Ashley Kuhl, Gregory M. Rice, Nicole Hoppman
Publikováno v:
Clinical Case Reports, Vol 7, Iss 6, Pp 1154-1160 (2019)
Abstract We report a two‐generation family with four females harboring an 8.5Mb heterozygous deletion of 5q15‐q21.2 who present with dysmorphic craniofacial features and speech delay. We hypothesize haploinsufficiency of CHD1 to be contributing t
Externí odkaz:
https://doaj.org/article/d7a5ae1ed0cd40d4baac3c82ab6f0a78
Autor:
Sujata Srikanth, Lavanya Jain, Cinthya Zepeda-Mendoza, Lauren Cascio, Kelly Jones, Rini Pauly, Barb DuPont, Curtis Rogers, Sara Sarasua, Katy Phelan, Cynthia Morton, Luigi Boccuto
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0253859 (2021)
Phelan-McDermid syndrome (PMS) is a multi-system disorder characterized by significant variability in clinical presentation. The genetic etiology is also variable with differing sizes of deletions in the chromosome 22q13 region and types of genetic a
Externí odkaz:
https://doaj.org/article/f1e267b546f04ca790d99f80fd77785b
Autor:
Jorge A, Trejo-Lopez, Corinne E, Praska, Cinthya, Zepeda Mendoza, Thomas M, Kollmeyer, Aditya, Raghunathan, Caterina, Giannini, Rachael A, Vaubel, Aivi, Nguyen, Mark E, Jentoft, Kliment, Donev, Gang, Zheng, Margaret A, DiGuardo, Benjamin R, Kipp, Robert B, Jenkins, Cristiane M, Ida
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 82:93-95
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0513fb4100ef369ef75daf244c2ff15
https://doi.org/10.1093/jnen/nlac102
https://doi.org/10.1093/jnen/nlac102
Autor:
Alaa Koleilat, Hongwei Tang, Neeraj Sharma, Huihuang Yan, Shulan Tian, James Smadbeck, Suganti Shivaram, Reid Meyer, Kathryn Pearce, Michael Baird, Cinthya Zepeda Mendoza, Xinjie Xu, Patricia T. Greipp, Jess F. Peterson, Rhett P. Ketterling, P. Leif Bergsagel, Celine Vachon, S. Vincent Rajkumar, Shaji Kumar, Yan W. Asmann, Eran Elhaik, Linda B. Baughn
Publikováno v:
Genetics in Medicine Open. :100816
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::374796bb0ac7ffb7b5008314890c75f2
https://doi.org/10.1016/j.gimo.2023.100816
https://doi.org/10.1016/j.gimo.2023.100816
Autor:
Cinthya Zepeda Mendoza, Anatasia Kellogg, Ashini Bolia, Brendan O'Fallon, Philippe Szankasi, Luobin Yang, Paul Rindler, Eric Fredrickson, Devin Close, Jay Patel, Xinjie Xu
Publikováno v:
Cancer Genetics. :44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1347a5a172a0c286ac3d870fa24654b
https://doi.org/10.1016/j.cancergen.2022.10.142
https://doi.org/10.1016/j.cancergen.2022.10.142
Autor:
Nadine Abdallah, Shaji Kumar, Jess F. Peterson, Neeraj Sharma, Yan W. Asmann, P. Leif Bergsagel, Patricia T. Greipp, Cinthya Zepeda-Mendoza, Kathryn E. Pearce, S. Vincent Rajkumar, Moritz Binder, Rhett P. Ketterling, James B. Smadbeck, Linda B. Baughn
Publikováno v:
Clin Cancer Res
Purpose: Structural variants (SV) of the MYC gene region are common in multiple myeloma and influence disease progression. However, the prognostic significance of different MYC SVs in multiple myeloma has not been clearly established. Experimental De
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb19dffbb2b99f7b672618f52c4db9f5
https://pubmed.ncbi.nlm.nih.gov/34233962
https://pubmed.ncbi.nlm.nih.gov/34233962