Výsledky vyhledávání - "T A, Iarocci"

Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities

Autor: GM Wagner, T A Iarocci, Peter A. Lane, William C. Mentzer, Narla Mohandas

Publikováno v: Blood. 71:1390-1396

This report describes a black family in which two distinct structural defects of alpha spectrin were inherited singly and in combination. The propositus, who has a poikilocytic hemolytic anemia that shares many of the features of hereditary pyropoiki

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b47d4a07eeee799094e87286e3e78bba
https://doi.org/10.1182/blood.v71.5.1390.1390

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Human embryonic zeta-globin chains in fetal and newborn blood

Autor: C. Mentzer, D. R. Higgs, David H.K. Chui, Stephen H. Embury, Susan P. Perrine, Margie Patterson, R. S. Mibashan, T. A. Iarocci

Publikováno v: Blood. 74:1409-1414

A sensitive and specific radioimmunoassay (RIA) for human embryonic zeta-globin chains was used to study normal fetal blood and newborn cord blood as well as cord blood from newborns with alpha-thalassemias. From 17 weeks until 37 weeks of gestation,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bf064dfb63893bde923e34b3cb4c5b3
https://doi.org/10.1182/blood.v74.4.1409.bloodjournal7441409

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Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome

Autor: B Smith, Narla Mohandas, William C. Mentzer, J Lazerson, T Hays, T A Iarocci, Peter A. Lane

Publikováno v: Journal of Clinical Investigation. 79:943-949

To explain the transient anemia and poikilocytosis seen during infancy in hereditary elliptocytosis (HE), we resealed erythrocyte (RBC) ghosts from affected children or their elliptocytic parents with 2,3-diphosphoglycerate (DPG) (0-8 mM), a compound

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d60d6c747439dd780ef11aa33461aaa7
https://doi.org/10.1172/jci112905

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Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis

Autor: T Hays, R L Shew, T A Iarocci, William C. Mentzer, Peter A. Lane, Narla Mohandas

Publikováno v: The Journal of clinical investigation. 79(3)

We report here a unique variant of alpha spectrin in a kindred with hereditary elliptocytosis. This novel red blood cell-membrane protein migrated to a position between the normal alpha- and beta-spectrin subunits in SDS polyacrylamide gel electropho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00875d4418691f426aa60ef103a6e04
https://pubmed.ncbi.nlm.nih.gov/3818958

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Human embryonic zeta-globin chains in fetal and newborn blood

Autor: D H, Chui, W C, Mentzer, M, Patterson, T A, Iarocci, S H, Embury, S P, Perrine, R S, Mibashan, D R, Higgs

Publikováno v: Blood. 74(4)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3eb9eb30c10adb06fdf297d612a3143e
https://pubmed.ncbi.nlm.nih.gov/2475189

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Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency

Autor: P. Höhn, William C. Mentzer, S. W. Eber, W. M. Lande, W. Schröter, T. A. Iarocci, James S. Wiley

Publikováno v: British journal of haematology. 72(3)

We studied the RBC membrane proteins of four patients, including a mother and daughter, with hereditary stomatocytosis. One- and two-dimensional gel electrophoresis revealed that a 28 kDa integral protein, present in normal RBC membranes, was absent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a27db3d109d93b90cf00dfa9c462bc6
https://pubmed.ncbi.nlm.nih.gov/2765409

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