Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Mary Risinger"'
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/840996a63d2c4519a193f1ac68e710b4
Autor:
Satheesh Chonat, Mary Risinger, Haripriya Sakthivel, Omar Niss, Jennifer A. Rothman, Loan Hsieh, Stella T. Chou, Janet L. Kwiatkowski, Eugene Khandros, Matthew F. Gorman, Donald T. Wells, Tamara Maghathe, Neha Dagaonkar, Katie G. Seu, Kejian Zhang, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Hereditary spherocytosis (HS) is the most common red blood cell (RBC) membrane disorder causing hereditary hemolytic anemia. Patients with HS have defects in the genes coding for ankyrin (ANK1), band 3 (SLC4A1), protein 4.2 (EPB42), and α (SPTA1) or
Externí odkaz:
https://doaj.org/article/ad840012f1744b04820b5b66c13c0ebd
Autor:
Mary Risinger, Phyllis S. Kim, Roberto X. Rodriguez, Monica Narvaez Rivas, Kenneth D. R. Setchell, Wenying Zhang, Theodosia A. Kalfa
Publikováno v:
American Journal of Hematology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a79a5d2d6d4323e1fda27a32e004d13e
https://doi.org/10.1002/ajh.26916
https://doi.org/10.1002/ajh.26916
Autor:
Panae Noomuna, John M. Hausman, Ruhani Sansoya, Theodosia Kalfa, Mary Risinger, Philip S. Low
Publikováno v:
FASEB J
Although both protein tyrosine phosphatases and kinases are constitutively active in healthy human red blood cells (RBCs), the preponderance of phosphatase activities maintains the membrane proteins in a predominantly unphosphorylated state. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd8b462e36d4b6c774c88e7e0b63b59f
https://doi.org/10.1096/fj.202100809rr
https://doi.org/10.1096/fj.202100809rr
Autor:
Mary Risinger, Theodosia A. Kalfa
Publikováno v:
Blood
The mature red blood cell (RBC) lacks a nucleus and organelles characteristic of most cells, but it is elegantly structured to perform the essential function of delivering oxygen and removing carbon dioxide from all other cells while enduring the she
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6b3d20e5ba91587b9251b946a7e755f
https://doi.org/10.1182/blood.2019000946
https://doi.org/10.1182/blood.2019000946
Publikováno v:
Hematology/Oncology Clinics of North America. 33:373-392
Hereditary hemolytic anemias (HHAs) comprise a heterogeneous group of anemias caused by mutations in genes coding the globins, red blood cell (RBC) membrane proteins, and RBC enzymes. Congenital dyserythropoietic anemias (CDAs) are rare disorders of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c27672082b664f025212eb6f0b273c2b
https://doi.org/10.1016/j.hoc.2019.01.002
https://doi.org/10.1016/j.hoc.2019.01.002
Autor:
Philip S. Low, Daniel A. Sheik, Sitong Zhou, Umut A. Gurkan, Ran An, Francesco Michelangelo Turrini, Katie Seu, Mary Risinger, Panae Noomuna, Yuncheng Man, Jane A. Little, Jiandi Wan, Theodosia A. Kalfa
Publikováno v:
Br J Haematol
British journal of haematology, vol 190, iss 4
British journal of haematology, vol 190, iss 4
Many hypotheses have been proposed to explain how a glutamate to valine substitution in sickle haemoglobin (HbS) can cause sickle cell disease (SCD). We propose and document a new mechanism in which elevated tyrosine phosphorylation of Band 3 initiat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fac6ddc451cc0569bbefb33f2624d3c3
https://europepmc.org/articles/PMC7606656/
https://europepmc.org/articles/PMC7606656/
Autor:
Georgios E Christakopoulos, Haripriya Sakthivel, Mary Risinger, Omar Niss, Harry Lesmana, Theodosia A. Kalfa
Publikováno v:
Blood. 130(Suppl_1)
Several members of the Ras-GTPases have been shown to play major roles as molecular switches in various signaling pathways in hematopoietic cells. The roles of Ras/MAPKs/ERK signaling pathways in EPO-induced erythroid differentiation have been explor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b932478572142c5d4b395636294d9784
https://pubmed.ncbi.nlm.nih.gov/31940662
https://pubmed.ncbi.nlm.nih.gov/31940662
Autor:
Umut A. Gurkan, Ran An, Sitong Zhou, Francesco Michelangelo Turrini, Daniel A. Sheik, Katie Seu, Mary Risinger, Theodosia A. Kalfa, Yuncheng Man, Jane A. Little, Jiandi Wan, Philip S. Low, Panae Noomuna
Publikováno v:
SSRN Electronic Journal.
Background: Sickle cell disease (SCD) derives from a mutation in sickle hemoglobin (HbS) that leads to vaso-occlusive events that eventually cause organ failure. Based on observations from multiple labs, we hypothesize that the events linking HbS den
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cdfdb5693e63c379c027971aeb12e19
https://doi.org/10.2139/ssrn.3514726
https://doi.org/10.2139/ssrn.3514726
Autor:
Marya Obaid Almansoori, Kejian Zhang, Karol Kerr, Theodosia A. Kalfa, Omar Niss, Neha Dagaonkar, Maa Ohui Quarmyne, Satheesh Chonat, Zora R. Rogers, Mary Risinger, Patrick T. McGann
Publikováno v:
Blood Cells, Molecules, and Diseases. 61:4-9
Hereditary elliptocytosis (HE) and hereditary pyropoikilocytosis (HPP) are heterogeneous red blood cell (RBC) membrane disorders that result from mutations in the genes encoding α-spectrin (SPTA1), β-spectrin (SPTB), or protein 4.1R (EPB41). The re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24158c75ecf1d56f8a49c94d10cae02
https://doi.org/10.1016/j.bcmd.2016.07.003
https://doi.org/10.1016/j.bcmd.2016.07.003