Zobrazeno 1 - 10
of 93
pro vyhledávání: '"George J. Dover"'
Autor:
George J. Dover, Rui Zhou, Neil A. Goldenberg, Keisuke Katsushima, Weihong Liang, Wei Liu, Ranjan J. Perera, Piyush Joshi
Publikováno v:
J Pediatr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::124d77ec28f4f7fd8e1dffeaa313556c
https://doi.org/10.1016/j.jpeds.2020.02.078
https://doi.org/10.1016/j.jpeds.2020.02.078
Publikováno v:
The Journal of Pediatrics. 169:272-276
To describe h- and g-indices benchmarks in pediatric subspecialties and general academic pediatrics. Academic productivity is measured increasingly through bibliometrics that derive a statistical enumeration of academic output and impact. The h- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b483a81304dd4dd04a5f3c3f698532c0
https://doi.org/10.1016/j.jpeds.2015.10.030
https://doi.org/10.1016/j.jpeds.2015.10.030
Publikováno v:
Pediatrics. 139(5)
The "7 Great Achievements in Pediatric Research" campaign noted discoveries in the past 40 years that have improved child and adult health in the United States and around the globe. This article predicts the next 7 great pediatric research advancemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2272ff9738c9896143e8b775f622b201
https://pubmed.ncbi.nlm.nih.gov/28557748
https://pubmed.ncbi.nlm.nih.gov/28557748
Autor:
David R. Williams, William W. Hay, Daniel P. Gitterman, Theodore C. Sectish, George J. Dover, Mark R. Schleiss
Publikováno v:
Pediatrics. 125:1259-1265
Although pediatric research enjoyed significant benefits during the National Institutes of Health (NIH) doubling era, the proportion of the NIH budget devoted to the pediatric-research portfolio has declined overall. In light of this declining suppor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb5c86b7cf72e3471454cca1d73f78d6
https://doi.org/10.1542/peds.2009-2635
https://doi.org/10.1542/peds.2009-2635
Autor:
Li Jun Weng, Jasper Manning, Steven D. Gore, Anchalee Jiemjit, Michelle A. Rudek, Hetty E. Carraway, George J. Dover, Stephen B. Baylin, Elizabeth A. Sugar, Michael R. Grever, James G. Herman, James A. Zwiebel, Abbie Mays, Oliver Galm, Ming Zhao, Judith E. Karp, Carole B. Miller, Anthony J. Murgo, Michael A. Carducci, B. Douglas Smith, Tianna Dauses
Publikováno v:
Cancer Research. 66:6361-6369
Optimal reexpression of most genes silenced through promoter methylation requires the sequential application of DNA methyltransferase inhibitors followed by histone deacetylase inhibitors in tumor cell cultures. Patients with myelodysplastic syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1858945ffce4b1513a28020036a38eb5
https://doi.org/10.1158/0008-5472.can-06-0080
https://doi.org/10.1158/0008-5472.can-06-0080
Publikováno v:
British Journal of Haematology. 126:606-611
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) disease in the Jamaican Cohort Study to determine whether there is evidence of distinct clustering of symptoms or clinical phenotypes. A twofold model yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61db9446731a47319119ad204c544703
https://doi.org/10.1111/j.1365-2141.2004.05025.x
https://doi.org/10.1111/j.1365-2141.2004.05025.x
Autor:
Linda M.S. Resar, Lorna K. Fitzpatric, Saul W. Brusilow, Alison M. Friedmann, Jodi B Segal, George J. Dover
Publikováno v:
Journal of Pediatric Hematology/Oncology. 24:737-741
This study was designed to determine if low doses of oral sodium phenylbutyrate (SPB) induce hemoglobin F (HbF) synthesis in children with hemoglobin SS (HbSS). We treated 8 children with HbSS over a period of 5-30 weeks. The initial dose (1.0 g/d) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dd814c027e57c2527048faa60d54366
https://doi.org/10.1097/00043426-200212000-00011
https://doi.org/10.1097/00043426-200212000-00011
The role of heterocellular hereditary persistence of fetal haemoglobin in β0-thalassaemia intermedia
Autor:
Raffaela Garau, Kirby D. Smith, Sergio Iannelli, Yen Pei C. Chang, Roberto Littera, Licinio Contu, Enrico Cacace, George J. Dover
Publikováno v:
British Journal of Haematology. 114:899-906
β0-thalassaemia intermedia (β0-TI) describes patients who lack β-globin synthesis yet manifest a non-transfusion-dependent form of β-thalassaemia. Co-inheritance of α-thalassaemia, certain variants of the β-like globin gene cluster and elevated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d032d3572d47edd4daf28735005906b
https://doi.org/10.1046/j.1365-2141.2001.03042.x
https://doi.org/10.1046/j.1365-2141.2001.03042.x
Autor:
George J. Dover, David H.K. Chui
Publikováno v:
Current Opinion in Pediatrics. 13:22-27
Patients who are homozygous for the sickle hemoglobin mutation can present with remarkably different clinical courses, varying from death in childhood, to recurrent painful vasoocclusive crises and multiple organ damage in adults, to being relatively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6243d0a87a22de955f6a53d8365be004
https://doi.org/10.1097/00008480-200102000-00004
https://doi.org/10.1097/00008480-200102000-00004
Publikováno v:
New England Journal of Medicine. 363:997-999
On April 13, 2010, the legislative council for Division I of the National Collegiate Athletic Association (NCAA) approved mandatory testing for sickle cell carrier status (sickle cell trait) for all student athletes participating in Division I sports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::896a3737b66819a66d46a8d1ec6ed45a
https://doi.org/10.1056/nejmp1007639
https://doi.org/10.1056/nejmp1007639