Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hongbo M. Xie"'
Autor:
Tatiana A. Karakasheva, Yusen Zhou, Hongbo M. Xie, Gloria E. Soto, Tiana D. Johnson, Madison A. Stoltz, Daana M. Roach, Noor Nema, Chizoba N. Umeweni, Kaitlyn Naughton, Lauren Dolinsky, James A. Pippin, Andrew D. Wells, Struan F.A. Grant, Louis Ghanem, Natalie Terry, Amanda B. Muir, Kathryn E. Hamilton
Publikováno v:
Gastro Hep Advances, Vol 2, Iss 6, Pp 830-842 (2023)
Background and Aims: A key histopathological feature of inflammatory bowel disease is damage to the mucosa, including breakdown of the epithelial barrier. Human enteroids and colonoids are a critical bench-to-bedside tool for studying the epithelium
Externí odkaz:
https://doaj.org/article/3b5bbb61491c43eda5c548a0bbb7c298
Pathogenicity and impact of HLA class I alleles in aplastic anemia patients of different ethnicities
Autor:
Timothy S. Olson, Benjamin F. Frost, Jamie L. Duke, Marian Dribus, Hongbo M. Xie, Zachary D. Prudowsky, Elissa Furutani, Jonas Gudera, Yash B. Shah, Deborah Ferriola, Amalia Dinou, Ioanna Pagkrati, Soyoung Kim, Yixi Xu, Meilun He, Shannon Zheng, Sally Nijim, Ping Lin, Chong Xu, Taizo A. Nakano, Joseph H. Oved, Beatriz M. Carreno, Yung-Tsi Bolon, Shahinaz M. Gadalla, Steven G.E. Marsh, Sophie Paczesny, Stephanie J. Lee, Dimitrios S. Monos, Akiko Shimamura, Alison A. Bertuch, Loren Gragert, Stephen R. Spellman, Daria V. Babushok
Publikováno v:
JCI Insight, Vol 7, Iss 22 (2022)
Acquired aplastic anemia (AA) is caused by autoreactive T cell–mediated destruction of early hematopoietic cells. Somatic loss of human leukocyte antigen (HLA) class I alleles was identified as a mechanism of immune escape in surviving hematopoieti
Externí odkaz:
https://doaj.org/article/d1c7bc07cfdf4986bc137dedb34e3f11
Autor:
Hongbo M. Xie, Kathrin M. Bernt
Publikováno v:
Biomolecules, Vol 12, Iss 8, p 1124 (2022)
Angiosarcoma is a rare, devastating malignancy with few curative options for disseminated disease. We analyzed a recently published genomic data set of 48 angiosarcomas and noticed recurrent amplifications of HOXA-cluster genes in 33% of patients. HO
Externí odkaz:
https://doaj.org/article/efb4fb125fff41fe9e4c433ddc2416e2
Autor:
Omobola O. Oluwafemi, Fadi I. Musfee, Laura E. Mitchell, Elizabeth Goldmuntz, Hongbo M. Xie, Hakon Hakonarson, Bernice E. Morrow, Tingwei Guo, Deanne M. Taylor, Donna M. McDonald-McGinn, Beverly S. Emanuel, A. J. Agopian
Publikováno v:
Genes, Vol 12, Iss 7, p 1030 (2021)
Conotruncal defects with normally related great vessels (CTD-NRGVs) occur in both patients with and without 22q11.2 deletion syndrome (22q11.2DS), but it is unclear to what extent the genetically complex etiologies of these heart defects may overlap
Externí odkaz:
https://doaj.org/article/669d47d7722e44b98a8e9c29fd5ee202
Autor:
Joshua A. Shapiro, Krutika S. Gaonkar, Stephanie J. Spielman, Candace L. Savonen, Chante J. Bethell, Run Jin, Komal S. Rathi, Yuankun Zhu, Laura E. Egolf, Bailey K. Farrow, Daniel P. Miller, Yang Yang, Tejaswi Koganti, Nighat Noureen, Mateusz P. Koptyra, Nhat Duong, Mariarita Santi, Jung Kim, Shannon Robins, Phillip B. Storm, Stephen C. Mack, Jena V. Lilly, Hongbo M. Xie, Payal Jain, Pichai Raman, Brian R. Rood, Rishi R. Lulla, Javad Nazarian, Adam A. Kraya, Zalman Vaksman, Allison P. Heath, Cassie Kline, Laura Scolaro, Angela N. Viaene, Xiaoyan Huang, Gregory P. Way, Steven M. Foltz, Bo Zhang, Anna R. Poetsch, Sabine Mueller, Brian M. Ennis, Michael Prados, Sharon J. Diskin, Siyuan Zheng, Yiran Guo, Shrivats Kannan, Angela J. Waanders, Ashley S. Margol, Meen Chul Kim, Derek Hanson, Nicholas Van Kuren, Jessica Wong, Rebecca S. Kaufman, Noel Coleman, Christopher Blackden, Kristina A. Cole, Jennifer L. Mason, Peter J. Madsen, Carl J. Koschmann, Douglas R. Stewart, Eric Wafula, Miguel A. Brown, Adam C. Resnick, Casey S. Greene, Jo Lynne Rokita, Jaclyn N. Taroni
Publikováno v:
Cell Genomics. :100340
Autor:
Shridhar Parthasarathy, Sarah M Ruggiero, Antoinette Gelot, Fernanda C Soardi, Bethânia F R Ribeiro, Douglas E V Pires, David B Ascher, Alain Schmitt, Caroline Rambaud, Hongbo M Xie, Laina Lusk, Olivia Wilmarth, Pamela Pojomovsky McDonnell, Olivia A Juarez, Alexandra N Grace, Julien Buratti, Cyril Mignot, Domitille Gras, Caroline Nava, Samuel R Pierce, Boris Keren, Benjamin C Kennedy, Sergio D J Pena, Ingo Helbig, Vishnu Anand Cuddapah
Heterozygous pathogenic variants in DNM1 cause developmental and epileptic encephalopathy (DEE) due to a dominant-negative mechanism impeding vesicular fission. Thus far, pathogenic variants in DNM1 have been studied using a canonical transcript that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eeaf7f665906b9dfae300d539e945ec
https://doi.org/10.1101/2022.06.02.492389
https://doi.org/10.1101/2022.06.02.492389
Autor:
Peter S, White, Hongbo M, Xie, Petra, Werner, Joseph, Glessner, Brande, Latney, Hakon, Hakonarson, Elizabeth, Goldmuntz
Publikováno v:
Birth defects research. Part A, Clinical and molecular teratology. 100(12)
We sought to characterize the landscape of structural variation associated with the subset of congenital cardiac defects characterized by left-sided obstruction.Cases with left-sided cardiac defects (LSCD) and pediatric controls were uniformly genoty
Autor:
Lisa C A, D'Alessandro, Petra, Werner, Hongbo M, Xie, Hakon, Hakonarson, Peter S, White, Elizabeth, Goldmuntz
Publikováno v:
Congenital heart disease. 9(1)
Left-sided cardiac lesions have a birth prevalence of approximately 1 in 1000 and have been shown to be heritable in pedigree studies. A large microdeletion at 16p12.1 is associated with childhood developmental delay, and initial studies describing t
Autor:
Zhe Zhang, Leipzig, Jeremy, Sasson, Ariella, Yu, Angela M., Perin, Juan C., Hongbo M. Xie, Sarmady, Mahdi, Warren, Patrick V., White, Peter S.
Publikováno v:
BMC Bioinformatics; 2013, Vol. 14 Issue Suppl 11, p1-10, 10p, 1 Diagram, 1 Chart, 7 Graphs