Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Moulds, Joann M."'
Autor:
Cockburn, Ian A., Mackinnon, Margaret J., O'Donnell, Angela, Allen, Stephen J., Moulds, Joann M., Baisor, Moses, Bockarie, Moses, Reeder, John C., Rowe, J. Alexandra
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2004 Jan 01. 101(1), 272-277.
Externí odkaz:
https://www.jstor.org/stable/3148410
Autor:
Rowe, J. Alexandra, Handel, Ian G., Thera, Mahamadou A., Deans, Anne-Marie, Lyke, Kirsten E., Koné, Abdoulaye, Diallo, Dapa A., Raza, Ahmed, Kai, Oscar, Marsh, Kevin, Plowe, Christopher V., Doumbo, Ogobara K., Moulds, Joann M.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2007 Oct . 104(44), 17471-17476.
Externí odkaz:
https://www.jstor.org/stable/25450259
Autor:
Moulds, Joann M.
Publikováno v:
In Clinics in Laboratory Medicine 2010 30(2):419-429
Publikováno v:
In Trends in Molecular Medicine 2002 8(11):531-537
Publikováno v:
American Journal of Hematology
The Rh D antigen posed both a significant clinical risk and inventory supply issue in transfusion medicine. The successful development of the immunocamouflaged RBC has the potential to address both the risk of acute anti‐D transfusion reactions and
Autor:
Moulds, Joann M. *, Zimmerman, Peter A., Doumbo, Ogobara K., Kassambara, Lalla, Sagara, Issaka, Diallo, Dapa A., Atkinson, John P., Krych-Goldberg, Malgorzata, Hauhart, Richard E., Hourcade, Dennis E., McNamara, David T., Birmingham, Daniel J., Rowe, J. Alexandra, Moulds, John J., Miller, Louis H.
Publikováno v:
In Blood 1 May 2001 97(9):2879-2885
Publikováno v:
Malaria Journal, Vol 4, Iss 1, p 54 (2005)
Abstract Background It has been hypothesized that the African alleles Sl2 and McCb of the Swain-Langley (Sl) and McCoy (McC) blood group antigens of the complement receptor 1 (CR1) may confer a survival advantage in the setting of Plasmodium falcipar
Externí odkaz:
https://doaj.org/article/ddace73fa03143a5bd02468633afb09d
Autor:
Mwesigwa, Savannah, Moulds, Joann M., Chen, Alice, Flanagan, Jonathan, Sheehan, Vivien A., George, Alex, Hanchard, Neil A.
BACKGROUND: Hyperhemolysis syndrome (HHS) is an uncommon, but life-threatening, transfusion-related complication of red blood cell transfusion. HHS has predominantly been described in patients with sickle cell disease (SCD) and is difficult to diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f145ddd61bf3ab1a1900a8bc356d5d4
https://europepmc.org/articles/PMC5847445/
https://europepmc.org/articles/PMC5847445/
Publikováno v:
BMC Genetics, Vol 4, Iss 1, p 14 (2003)
Abstract Background Aberrant and non-functional RHD alleles are much more frequent in Africans than in Europeans. The DAU cluster of RHD alleles exemplifies that the alleles frequent in Africans have evaded recognition until recently. A comprehensive
Externí odkaz:
https://doaj.org/article/846ae2c250d44ae7a3cffa09a70fa516
Autor:
Thathy, Vandana1 vthathy@wrp-ksm.org, Moulds, JoAnn M.2,3 jmmoulds@lifeshare.org, Guyah, Bernard1 Bguyah@wrp-ksm.org, Otieno, Walter1 Wotieno@wrp-ksm.org, Stoute, José A.4,5 jose.stoute@us.army.mil
Publikováno v:
Malaria Journal. 2005, Vol. 4, p54-7. 7p.