Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Juan Salomon-Andonie"'
Autor:
Xiaomei Niu, Christian S. Parry, Angela Mason, Barbara Harrison, Seyed Mehdi Nouraie, Tatiana Ammosova, Juan Salomon-Andonie, Patricia A. Oneal, Victor R. Gordeuk, James G. Taylor, null VI, Sergei Nekhai
Publikováno v:
Journal of Hematology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd48fb831e0765262600405b19011263
https://pubmed.ncbi.nlm.nih.gov/32855759
https://pubmed.ncbi.nlm.nih.gov/32855759
Autor:
James G. Taylor, Juan Salomon-Andonie, Marilyn J. Telen, Ester Sabino, Victor R. Gordeuk, Allison E. Ashley-Koch, Yingze Zhang, Mark T. Gladwin, Xu Zhang, Quenna Wong, Fayuan Wen, Gulriz Kurban, Angela Rock, Xiaomei Niu, Shannon Kelly, Songping Wang, Sergei Nekhai, Seyed Mehdi Nouraie, Brian Custer, Carla Luana Dinardo
Publikováno v:
Blood. 136:52-52
Introduction: Transfusional iron (Fe) overload is a significant problem among patients with chronic, transfusion-dependent anemias. Iron overload is an important problem in pediatric sickle cell disease (SCD) patients on chronic transfusion regimens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e830d8add80b439d6da6f0454b591865
https://doi.org/10.1182/blood-2020-142809
https://doi.org/10.1182/blood-2020-142809
Autor:
James G. Taylor, Lydie Ocini Ngolet, Juan Salomon-Andonie, Alexis Elira Dokekias, Sergei Nekhai
Publikováno v:
Blood advances. 2(Suppl 1)
The Republic of Congo (RC) ([Figure 1][1]) has one of highest prevalence rates of sickle cell trait (SCT) in the world. The prevalence of sickle cell disease (SCD) is estimated to be at least 1.5% with an expected nationwide SCD patient population of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f4dbf53f5a87e069f7fd2b36be9a9e7
https://pubmed.ncbi.nlm.nih.gov/30504190
https://pubmed.ncbi.nlm.nih.gov/30504190
Autor:
Juan Salomon-Andonie, Donghoon Yoon, Sabina Swierczek, Donald A. McClain, Lydia A. Polyakova, Khadega A. Abuelgasim, Galina Y. Miasnikova, Rabia Cherqaoui, Xiaomei Niu, Daniel J. Okhotin, Adelina I. Sergueeva, M. Celeste Simon, Victor R. Gordeuk, Mehdi Nouraie, Jingyu Huang, James E. Cox, Josef T. Prchal, Jihyun Song, Judith Simcox, David Okhotin
Publikováno v:
Journal of Molecular Medicine. 91:59-67
In Chuvash polycythemia, a homozygous 598CT mutation in the von Hippel-Lindau gene (VHL) leads to an R200W substitution in VHL protein, impaired degradation of α-subunits of hypoxia-inducible factor (HIF)-1 and HIF-2, and augmented hypoxic responses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9032349eec4a9c681977c10d5f7b2d4c
https://doi.org/10.1007/s00109-012-0961-5
https://doi.org/10.1007/s00109-012-0961-5
Autor:
Juan Salomon-Andonie, Victor R. Gordeuk, Lydia A. Polyakova, Sergei Nekhai, Xiaomei Niu, Galina Y. Miasnikova, Adelina I. Sergueeva
To the editor: Hypoxia inducible factor (HIF)-1 and HIF-2 are transcription factors that play a major role in cellular responses to hypoxia. Levels of the α subunits of HIFs are constantly degraded under normoxia by the proteasome through an interac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a26d0bfd59f624375efea049acc910e
https://europepmc.org/articles/PMC3811180/
https://europepmc.org/articles/PMC3811180/
