Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kori Bradley"'
Publikováno v:
Experimental and Clinical Transplantation. 17:470-477
OBJECTIVES Long-term outcomes of kidney transplant recipients with postoperative genitourinary tract infections are not well characterized. In this single center retrospective study, we aimed to investigate the long-term effects of early posttranspla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c8c5a1d08f3059748668b28dfdfe80
https://doi.org/10.6002/ect.2017.0196
https://doi.org/10.6002/ect.2017.0196
Autor:
Amit K. Mathur, Kori Bradley, Randall S. Sung, Steven Kapeles, John T. Stoffel, Dushyanth Srinivasan
Publikováno v:
Annals of transplantation. 21
Background Long-term outcomes of kidney transplantation recipients with bladder dysfunction or prior bladder surgery are not well characterized. Material and methods Electronic records of 1753 recipients of kidney-alone transplant between January 200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d7725286bf4c3fd944ebf750e4191ce
https://pubmed.ncbi.nlm.nih.gov/27090659
https://pubmed.ncbi.nlm.nih.gov/27090659
Autor:
Keiji Tanimoto, Shuaiying Cui, Andrew D. Campbell, Lihong Shi, Lindsay A. Schmidt, David Harro, Andrea Mathias, Brittne Halford, Rhonda Douglas, Rebekah Urbonya, Donald A. Giacherio, Kwaku Osei Bonsu, Osamu Tanabe, Kori Bradley, James Douglas Engel
Publikováno v:
Proceedings of the National Academy of Sciences. 108:18808-18813
Sickle cell disease (SCD) is a hematologic disorder caused by a missense mutation in the adult β-globin gene. Higher fetal hemoglobin (HbF) levels in red blood cells of SCD patients have been shown to improve morbidity and mortality. We previously f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9136385a2cfe14503d7f8357734b6bcf
https://doi.org/10.1073/pnas.1104964108
https://doi.org/10.1073/pnas.1104964108
Autor:
Kori Bradley, Jintao Wang, Hui Wang, Wei Luo, Daniel T. Eitzman, Andrew D. Campbell, Chiao Guo
Publikováno v:
Blood. 120:3862-3864
To the editor: Sickle cell disease (SCD) is a hemoglobinopathy caused by a single amino acid change in the β globin subunit that predisposes hemoglobin to abnormal polymerization leading to stiff, sickled erythrocytes, and microvascular occlusions.[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d7b5d1d6b924e766efb497ef33a5d1b
https://doi.org/10.1182/blood-2012-07-444455
https://doi.org/10.1182/blood-2012-07-444455
Publikováno v:
Journal of Urology. 191
INTRODUCTION AND OBJECTIVES: A substantial proportion of kidney transplantation recipients have bladder dysfunction or have had bladder substitutions. We compared graft survival and post operative morbidity of these recipients after transplant to rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2356ecaa453335b5fb7aa25a79f48aaa
https://doi.org/10.1016/j.juro.2014.02.2251
https://doi.org/10.1016/j.juro.2014.02.2251
Publikováno v:
Transplantation Direct
Background Long-term outcomes of kidney transplantation recipients with percutaneous ureteral management of transplant ureteral complications are not well characterized. Methods Electronic records of 1753 recipients of kidney-alone transplant between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5bcaa18cec894a95c294056b85e13f7
https://doi.org/10.1097/txd.0000000000000637
https://doi.org/10.1097/txd.0000000000000637
Autor:
Jintao Wang, Wei Luo, Kori Bradley, Julia Wang, Stephanie L. Wolffe, Eddy B. Sun, Hui Wang, Chiao Guo, Andrew D. Campbell, Daniel T. Eitzman
Publikováno v:
British journal of haematology. 162(1)
Sickle cell disease (SCD) is associated with vascular complications including premature stroke. The role of atherothrombosis in these vascular complications is unclear. To determine the effect of SCD on atherosclerosis and thrombosis, mice with SCD a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0df9cb7524298ae468a0cca9ee74234
https://pubmed.ncbi.nlm.nih.gov/23590132
https://pubmed.ncbi.nlm.nih.gov/23590132
Autor:
Shuaiying Cui, Osamu Tanabe, Andrew D. Campbell, Ama Amachong, Jennifer Addo, Rebekah Urbonya, Kori Bradley, David Harro, David Giacherio, Lihong Shi, Kwaku Osei Bonsu
Publikováno v:
Blood. 120:3248-3248
Abstract 3248 Background: Fetal Hemoglobin (Hgb F)has been shown to improve morbidity and mortality with SCD patients. We recently published that forced expression of TR2/TR4 resulted in 2.5 fold induction of Fetal Hemoglobin and improved phenotypes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf9e2fe9d3b361d48e9f443d0eb6f172
https://doi.org/10.1182/blood.v120.21.3248.3248
https://doi.org/10.1182/blood.v120.21.3248.3248