Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jill F. Falcone"'
Publikováno v:
Journal of Biological Chemistry. 278:39565-39571
Hemoglobin function can be modulated by the red cell membrane but some mechanistic details are incomplete. For example, the 43-kDa chymotryptic fragment of the cytoplasmic portion of red cell membrane Band 3 protein and its corresponding N-terminal 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6c5dc5bdee815ec54340300af403b8f
https://doi.org/10.1074/jbc.m303352200
https://doi.org/10.1074/jbc.m303352200
Autor:
Jill F. Falcone, Orah S. Platt
Publikováno v:
Blood. 86:1992-1998
The pattern of membrane abnormalities in sickle red blood cells suggests that sickle hemoglobin damages membrane proteins. We have previously shown a functional defect in sickle ankyrin, poor spectrin- binding ability. Here we examine the other major
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb4343133c2481178d883e951d3c7a22
https://doi.org/10.1182/blood.v86.5.1992.bloodjournal8651992
https://doi.org/10.1182/blood.v86.5.1992.bloodjournal8651992
Autor:
D. Holmes Morton, Marcin W. Wlodarski, Joachim B. Kunz, Jill F. Falcone, Kevin H.M. Kuo, Wendy B. London, Heng Wang, Kerri Nottage, Bertil Glader, Alexis A. Thompson, Yves D. Pastore, Jennifer A. Rothman, Melissa J. Rose, Eduard J. van Beers, Peter E. Newburger, Stefan W. Eber, Mukta Sharma, Jenny M Depsotovic, Hassan M. Yaish, Yaddanapudi Ravindranath, Christine M. Knoll, Patricia J. Giardina, Dongjing Guo, Vicky R. Breakey, Ellis J. Neufeld, Rachael F. Grace, Wilma Barcellini, Melissa Rhodes
Publikováno v:
ResearcherID
Background: An international, multicenter registry was established to collect clinical data on patients with PKD, the most common glycolytic defect causing congenital non-spherocytic hemolytic anemia. Aim: To describe and categorize the phenotypic sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcf6bb9166ee1282fa04b7434544d6dd
https://doi.org/10.1182/blood.v126.23.2136.2136
https://doi.org/10.1182/blood.v126.23.2136.2136
Autor:
Adam Bagg, Robin Casey, Jill F. Falcone, Inderneel Sahai, Elizabeth O. Hexner, Lulu Mathews, Anke K. Bergmann, Klaas J. Wierenga, Caterina Borgna-Pignati, Luca Fabris, Maria Leticia Ribeiro, Judy Fleming, Ellis J. Neufeld
Publikováno v:
The Journal of Pediatrics. 155:888-892.e1
Objective To determine causative mutations and clinical status of 7 previously unreported kindreds with TRMA syndrome, (thiamine-responsive megaloblastic anemia, online Mendelian inheritance in man, no. 249270), a recessive disorder of thiamine trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8d23913e93cac91499dce0d83dc155
https://doi.org/10.1016/j.jpeds.2009.06.017
https://doi.org/10.1016/j.jpeds.2009.06.017
Publikováno v:
Journal of Clinical Investigation. 75:266-271
Although functional abnormalities of the sickle erythrocyte membrane skeleton have been described, there is little quantitative data on the function of the proteins that compose the skeleton. We have examined the association of spectrin, the major sk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d5a8e34c8abad29876158c3d9cc4963
https://doi.org/10.1172/jci111684
https://doi.org/10.1172/jci111684