Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Harvest Mariki"'
Autor:
Siana Nkya Mtatiro, Tarjinder Singh, Helen Rooks, Josephine Mgaya, Harvest Mariki, Deogratius Soka, Bruno Mmbando, Evarist Msaki, Iris Kolder, Swee Lay Thein, Stephan Menzel, Sharon E Cox, Julie Makani, Jeffrey C Barrett
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111464 (2014)
Fetal hemoglobin (HbF) is an important modulator of sickle cell disease (SCD). HbF has previously been shown to be affected by variants at three loci on chromosomes 2, 6 and 11, but it is likely that additional loci remain to be discovered.We conduct
Externí odkaz:
https://doaj.org/article/36304838133a4c1aa3a02d07da489ce3
Autor:
Raphael Z. Sangeda, Bruno Mmbando, Edward Kija, Furahini Tluway, Elisha Osati, Abel Makubi, Evarist Msaki, Julie Makani, Siana Nkya, Harvest Mariki, Florence Urio, Musa Makongoro, Deogratias Soka, Magdalena Lyimo, Christina Kindole, Josephine Mgaya, Stella Rwezaura
Publikováno v:
Tanzania Medical Journal. 31:106-119
Background: The pathophysiology of sickle cell disease (SCD) is complex and involves nitric oxide depletion, increased inflammation/adhesion molecules and vaso-occlusion in addition to the chronic hemolytic anemia. This pathophysiology results in sys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::229cd7fd962d6045b45a3a55cdd3d550
https://doi.org/10.4314/tmj.v31i1.346
https://doi.org/10.4314/tmj.v31i1.346
Autor:
Harvest Mariki, Stephan Menzel, Julie Makani, Jeffrey C. Barrett, Bruno Mmbando, Tarjinder Singh, Deogratius Soka, Helen Rooks, Sharon E. Cox, Josephine Mgaya, Siana Nkya Mtatiro, Swee Lay Thein
Publikováno v:
BMC Medical Genetics
BACKGROUND: Common genetic variants residing near upstream regulatory elements for MYB, the gene encoding transcription factor cMYB, promote the persistence of fetal hemoglobin (HbF) into adulthood. While they have no consequences in healthy individu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::327a1f862d34cd20df52388383906d5d
https://doi.org/10.1186/s12881-015-0148-3
https://doi.org/10.1186/s12881-015-0148-3
Autor:
Julie Makani, Stephan Menzel, Deogratius Soka, Sharon E. Cox, Josephine Mgaya, Bruno P. Mmbando, Tarjinder Singh, Siana Nkya Mtatiro, Evarist Msaki, Harvest Mariki, Swee Lay Thein, Helen Rooks, Iris C. R. M. Kolder, Jeffrey C. Barrett
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 11, p e111464 (2014)
PLoS ONE, Vol 9, Iss 11, p e111464 (2014)
BACKGROUND: Fetal hemoglobin (HbF) is an important modulator of sickle cell disease (SCD). HbF has previously been shown to be affected by variants at three loci on chromosomes 2, 6 and 11, but it is likely that additional loci remain to be discovere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::233ef4f9de7a1372e53383aa64b08156
http://ihi.eprints.org/3779/
http://ihi.eprints.org/3779/
