Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Helge Hartung"'
Supplementary Figures and Tables
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6649a8801e88917050969e78fb350424
https://doi.org/10.1158/0008-5472.22367795.v1
https://doi.org/10.1158/0008-5472.22367795.v1
The t(2;11)(q31;p15) chromosomal translocation results in a fusion between the NUP98 and HOXD13 genes and has been observed in patients with myelodysplastic syndrome (MDS) or acute myelogenous leukemia. We previously showed that expression of the NUP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e474eccba1783d6ec9bdac368d50343
https://doi.org/10.1158/0008-5472.c.6495692
https://doi.org/10.1158/0008-5472.c.6495692
Autor:
Jessica A. Pollard, Elissa Furutani, Shanshan Liu, Erica Esrick, Laurie E. Cohen, Jacob Bledsoe, Chih-Wei Liu, Kun Lu, Maria Jose Ramirez de Haro, Jordi Surrallés, Maggie Malsch, Ashley Kuniholm, Ashley Galvin, Myriam Armant, Annette S. Kim, Kaitlyn Ballotti, Lisa Moreau, Yu Zhou, Daria Babushok, Farid Boulad, Clint Carroll, Helge Hartung, Amy Hont, Taizo Nakano, Tim Olson, Sei-Gyung Sze, Alexis A. Thompson, Marcin W. Wlodarski, Xuesong Gu, Towia A. Libermann, Alan D’Andrea, Markus Grompe, Edie Weller, Akiko Shimamura
Publikováno v:
Blood advances. 6(12)
Fanconi anemia (FA), a genetic DNA repair disorder characterized by marrow failure and cancer susceptibility. In FA mice, metformin improves blood counts and delays tumor development. We conducted a single institution study of metformin in nondiabeti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edfdac07a07a7ba4a3ce114f4b122dbb
https://pubmed.ncbi.nlm.nih.gov/35500223
https://pubmed.ncbi.nlm.nih.gov/35500223
Publikováno v:
Clinical Imaging. 56:52-57
To determine the optimal MRI protocol and sequences for liver and cardiac iron estimation in children.We evaluated patients ≤18 years with cardiac and liver MRIs for iron content estimation. Liver T2 was determined by a third-party company. Cardiac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd336c94ee7299d4b7134055ff312c8c
https://doi.org/10.1016/j.clinimag.2019.02.012
https://doi.org/10.1016/j.clinimag.2019.02.012
Autor:
Helge Hartung, Sarah Rottenberg
Publikováno v:
Academic Entrepreneurship for Medical and Health Sciences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3983e2dd091a76c2c37fd1fed5b0784
https://doi.org/10.21428/b2e239dc.1d894adb
https://doi.org/10.21428/b2e239dc.1d894adb
Autor:
Ryan Brandon Hunter, Joshua Nicklas, Flaura Koplin Winston, Kelsey Oh, Paul Dehel, Helge Hartung
Publikováno v:
Academic medicine : journal of the Association of American Medical Colleges. 96(4)
Problem There is a clear and urgent need for health care innovation in the United States. Hospital employees routinely recognize pain points that affect care delivery and are in a unique position to propose innovative and practical solutions, yet lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30c272342892efa0f7d6cfba8fea11c
https://pubmed.ncbi.nlm.nih.gov/33208677
https://pubmed.ncbi.nlm.nih.gov/33208677
Autor:
Jason E. Farrar, Anupama Narla, Kelly Walkovich, Helge Hartung, Grzegorz Nalepa, Adrianna Vlachos, Evangelia Atsidaftos, Jeffrey M. Lipton, Mohammad Lutfi Lababidi, Jonathan Bernstein, Ellen Muir, Zora R. Rogers, Thomas W. Loew, Waseem Alhushki, Colin A. Sieff, Bertil Glader, Barbara Gruner, Christine M. Knoll, Arun R Panigrahi
Publikováno v:
Pediatr Blood Cancer
Background Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, short stature, congenital anomalies, and cancer predisposition. Most cases are due to mutations in genes encoding ribosomal proteins (RP) l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f35da0422ca685604b2d6c0cfaafb63
https://europepmc.org/articles/PMC8273758/
https://europepmc.org/articles/PMC8273758/
Autor:
Angela M. Ellison, Aileen Schast, Therese McKnight, Marlena Kittick, Helge Hartung, Erin Coyne, Cynthia F. Norris, Jane Lavelle, Kim Smith Whitley
Publikováno v:
Journal of Pediatric Hematology/Oncology. 40:111-115
Background and objective Recurrent hospital admissions for patients with sickle cell disease (SCD) are costly and contribute to a low quality of life for patients. We implemented a clinical pathway to safely discharge SCD patients with fever who are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b4067268dddc10a4f3f2068b4b3125
https://doi.org/10.1097/mph.0000000000001052
https://doi.org/10.1097/mph.0000000000001052
Autor:
Charles T. Quinn, Alexis A. Thompson, Anna M Hood, Jasmine Stallworth, Constance A. Mara, Yolanda Johnson, Emily Riehm Meier, Helge Hartung, Lisa M Shook, Lori E. Crosby, Kim Smith-Whitley, Allison A. King, Venee N. Tubman, Stacey M. Gomes, Amber M Yates, Aimee K. Hildenbrand, Jean L. Raphael, Joanna Rebitski, Catharine Whitacre, Sherif M. Badawy, Neha Bhasin, Steven K Reader, Susan E Creary
Publikováno v:
Blood
Background: Hydroxyurea (HU) is the primary medication used to prevent the significant medical and neurologic morbidities of pediatric sickle cell disease (SCD; HbSS or HbSB0 thalassemia). Despite the benefits of HU, it remains under-utilized likely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2e72a52050517f6717565dda6a149dc
https://doi.org/10.1182/blood-2021-152722
https://doi.org/10.1182/blood-2021-152722
Autor:
Jacob Bledsoe, Farid Boulad, Annette S. Kim, Laurie E. Cohen, Kaitlyn Ballotti, Elissa M. Furutani, Maggie Malsch, Marcin W. Wlodarski, Amy Hont, María José Ramírez, Erica B. Esrick, Alexis A. Thompson, Edie Weller, Jessica A. Pollard, Alan D. D'Andrea, Jordi Surrallés, Ashley Kuniholm, Ashley Galvin, Towia A. Libermann, Clinton Carroll, Akiko Shimamura, Kun Lu, Lisa A. Moreau, Shanshan Liu, Helge Hartung, Daria V. Babushok, Sei-Gyung K. Sze, Yu Zhou, Myriam Armant, Markus Grompe, Taizo A. Nakano, Timothy S. Olson
Publikováno v:
Blood. 138:1102-1102
Fanconi anemia (FA), a genetic disorder affecting DNA repair, is characterized by bone marrow failure and cancer susceptibility. In FA mouse models, metformin (N,N-dimethylguanide) a biguanide metabolic agent, improves blood counts and delays tumor d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8988dfb489d3161e305f8e7c38eae98c
https://doi.org/10.1182/blood-2021-153598
https://doi.org/10.1182/blood-2021-153598