Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Diane, Kissell"'
Autor:
Parinda A. Mehta, Ashley Teusink, Kejian Zhang, Sarah Dell, Tsuyoshi Fukuda, Shannon Nortman, Adam Lane, Diane Kissell, Stella M. Davies, Alexander A. Vinks, Alexandra H. Filipovich
Publikováno v:
Biology of Blood and Marrow Transplantation. 22:482-486
Invasive fungal infections are a significant cause of morbidity and mortality in recipients of hematopoietic stem cell transplantation (HSCT), warranting antifungal prophylaxis as a standard of care in these patients. Voriconazole is commonly used in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d22f950c6ec1957c8d68a66e162289e
https://doi.org/10.1016/j.bbmt.2015.11.011
https://doi.org/10.1016/j.bbmt.2015.11.011
Publikováno v:
Pediatric dermatology. 35(2)
Background Historically, diagnosis of epidermolysis bullosa has required skin biopsies for electron microscopy, direct immunofluorescence to determine which gene(s) to choose for genetic testing, or both. Methods To avoid these invasive tests, we dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::399c013760fc468a0db29e0cd1fdaac8
https://pubmed.ncbi.nlm.nih.gov/30211458
https://pubmed.ncbi.nlm.nih.gov/30211458
Autor:
Lisa R. Young, Chrysi Kanellopoulou, Kejian Zhang, Shannon Nortman, Hilary Haines, Jill M. Fritz, Jason D. Hughes, Susan Price, Michael J. Lenardo, Wei Lu, Yu Zhang, Diane Kissell, Helen C. Su, Rebecca A. Marsh, Vijaya Chaturvedi, Michael B. Jordan, Jack J. Bleesing, Zhiduo Liu, Michael C. Stephens, Joshua J McElwee, Peter Mustillo, Lixin Zheng, Elif Karakoc-Aydiner, Helen F. Matthews, Jun Mo, V. Koneti Rao, Bernice Lo, Alexandra H. Filipovich, Kasper Hoebe, Cesar M. Rueda, Ammar Husami, Claire A. Chougnet, Qian Zhang
Publikováno v:
Science. 349:436-440
Trafficking from bedside to bench Typically in translational research, a discovery in cell or molecular biology is later exploited to improve patient care. Occasionally, information flows in the opposite direction. Lo et al. found that patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a164d731b5c4eba5dcc14b3d2978cd
https://doi.org/10.1126/science.aaa1663
https://doi.org/10.1126/science.aaa1663
Autor:
Cassandra Perry, Matthew Veerkamp, Brooke M McLaughlin, Melanie F. Myers, Xue Zhang, Cynthia A. Prows, Kejian Zhang, Diane Kissell, Ingrid A. Holm
Aim: To determine parents’ use of their children's CYP2D6 research result. We hypothesized that perceived utility, likelihood of sharing and actual sharing of results would differ between parents with children previously exposed (cases) or unexpose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c7fe0551815285b53d0f13641a4c86c
https://europepmc.org/articles/PMC5827812/
https://europepmc.org/articles/PMC5827812/
Autor:
Diane Kissell, Alexandra H. Filipovich, Jessica A Connor, Nathaniel Barasa, Ammar Husami, Matthew T. Weirauch, C. Alexander Valencia, Yaping Qian, Kejian Zhang, Judith Johnson, Jeffery Schubert, Ge Zhang
Publikováno v:
Pediatric Blood & Cancer. 61:1034-1040
Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disorder due to dysregulation of the immune system.The predominant symptoms are persistent fever, cytopenias,hepatosplenomegaly, hepatitis, sometimes associated with hyper-ferritine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c239fcb601dfcc98f0f016d21fc1eb
https://doi.org/10.1002/pbc.24955
https://doi.org/10.1002/pbc.24955
Autor:
Julie M. Schultz, Megan Flanagan, Theru A. Sivakumaran, Mohsin Shahzad, Kejian Zhang, Thomas B. Friedman, Zawar Hussain, Sheikh Riazuddin, Diane Kissell, Zubair M. Ahmed, Munir Ahmad Bhinder, Shaheen N. Khan, Saima Riazuddin, John H. Greinwald, Tanveer A. Qaiser
Publikováno v:
Otolaryngology–Head and Neck Surgery. 149:478-487
To identify the genetic cause of prelingual sensorineural hearing loss in Pakistani families using a next-generation sequencing (NGS)-based mutation screening test named OtoSeq.Prospective study.Research laboratory.We used 3 fluorescently labeled sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c453cb5734bd1b344d815960a400715f
https://doi.org/10.1177/0194599813493075
https://doi.org/10.1177/0194599813493075
Autor:
Kejian Zhang, Diane Kissell, Michael B. Jordan, Jarek Meller, Joyce Villanueva, Alexandra H. Filipovich, Kimberly A. Risma, Judith Johnson, Peter S. Klein, Qian Wei, Rebecca A. Marsh
Publikováno v:
Blood. 118:5794-5798
Familial hemophagocytic lymphohistiocytosis (HLH) is a rare primary immunodeficiency disorder characterized by defects in cell-mediated cytotoxicity that results in fever, hepatosplenomegaly, and cytopenias. Familial HLH is well recognized in childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::066bba43a36cd266f2cb8a25964dada1
https://doi.org/10.1182/blood-2011-07-370148
https://doi.org/10.1182/blood-2011-07-370148
Autor:
Tatiana Foroud, Karen Marder, William C. Nichols, Alice Rudolph, Ronald F. Pfeiffer, Michael W. Pauciulo, Diane Kissell, Cheryl Halter, Nathan Pankratz
Publikováno v:
Neurology. 73:279-286
Objective: Mutations in both alleles of parkin have been shown to result in Parkinson disease (PD). However, it is unclear whether haploinsufficiency (presence of a mutation in only 1 of the 2 parkin alleles) increases the risk for PD. Methods: We pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169e1ecc08542d7a0dad1e8fefb8238b
https://doi.org/10.1212/wnl.0b013e3181af7a33
https://doi.org/10.1212/wnl.0b013e3181af7a33
Autor:
Diane Kissell, Kristi A. Clark, Tatiana Foroud, Ronald F. Pfeiffer, V. E. Elsaesser, Alice Rudolph, William C. Nichols, Joanne Wojcieszek, Cheryl Halter, Michael W. Pauciulo, Nathan Pankratz
Publikováno v:
Neurology. 72:1886-1892
Objective: A recent study reported that mutations in a gene on chromosome 2q36-37, GIGYF2 , result in Parkinson disease (PD). We have previously reported linkage to this chromosomal region in a sample of multiplex PD families, with the strongest evid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732a67ce8c450f384c38d5e740111f51
https://doi.org/10.1212/01.wnl.0000346517.98982.1b
https://doi.org/10.1212/01.wnl.0000346517.98982.1b
Autor:
Alexei A. Grom, Ndate Fall, Kejian Zhang, Randy Q. Cron, Mingce Zhang, Grant S. Schulert, Andrew Hanosh, Ammar Husami, Lena M. Napolitano, Lauren B. Smith, Paul W. Harms, Javed Siddiqui, Kristina Davis, Jeffrey M. Jentzen, Diane Kissell
Publikováno v:
The Journal of infectious diseases. 213(7)
Background. Severe H1N1 influenza can be lethal in otherwise healthy individuals and can have features of reactive hemophagocytic lymphohistiocytosis (HLH). HLH is associated with mutations in lymphocyte cytolytic pathway genes, which have not been p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05eb53b621d488fa61d343f5bac9432e
https://pubmed.ncbi.nlm.nih.gov/26597256
https://pubmed.ncbi.nlm.nih.gov/26597256