Zobrazeno 1 - 10
of 15
pro vyhledávání: '"hemoglobin d-los angeles"'
Autor:
A A PETRENKO, A V PIVNIK, P P KIM, E Yu DEMIDOVA, V L SURIN, A O ABDULLAEV, A B SUDARIKOV, N A PETROVA, S A MARYINA
Publikováno v:
Терапевтический архив, Vol 90, Iss 7, Pp 105-109 (2018)
Thalassemia and qualitative hemoglobinopathy are hereditary disorders of Hb synthesis that lead to change in the Hb conformation or a decrease in the synthesis of structurally normal Hb, and consequently, to erythron pathology. Many variants of Hb ar
Externí odkaz:
https://doaj.org/article/1bc3a740a1b64521aa70f4f07550d5df
Autor:
Patrícia H. O. Calderan, Rute Blasi de Oliveira, Ana R. Chinelato-Fernandes, Claudia Regina Bonini Domingos, Guilherme G. Leoneli, Claudia Augusta Hidalgo, Wilson A. Silva
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 25, Iss 3, Pp 161-168 (2003)
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Revista Brasileira de Hematologia e Hemoterapia v.25 n.3 2003
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
SciELO
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Revista Brasileira de Hematologia e Hemoterapia v.25 n.3 2003
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Submitted by Guilherme Lemeszenski (guilherme@nead.unesp.br) on 2013-08-22T18:40:35Z No. of bitstreams: 1 S1516-84842003000300007.pdf: 98127 bytes, checksum: 0fb56fda2526013d5caefa9e67f6dacf (MD5) Made available in DSpace on 2013-08-22T18:40:35Z (GMT
Autor:
Ana R. Chinelato-Fernandes, Guilherme G. Leoneli, Patrícia O. Calderan, Rute Blasi de Oliveira, Wilson Araújo da Silva Jr., Claudia Augusta Hidalgo, Claudia Regina Bonini- Domingos
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 25, Iss 3, Pp 161-168 (2003)
A variante de hemoglobina (Hb) D mais comum, Hb D Los Angeles ou D Punjab, é originada de uma transversão GAA->CAA no códon 121 da globina beta; essa mutação resulta na substituição do ácido glutâmico por glutamina na proteína. É a terceir
Akademický článek
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Autor:
Chinelato-Fernandes, Ana R., Leoneli, Guilherme G., Calderan, Patrícia O., Oliveira, Rute Blasi de, Silva Jr., Wilson Araújo da, Hidalgo, Claudia Augusta, Bonini- Domingos, Claudia Regina
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Volume: 25, Issue: 3, Pages: 161-168, Published: 2003
A variante de hemoglobina (Hb) D mais comum, Hb D Los Angeles ou D Punjab, é originada de uma transversão GAA->CAA no códon 121 da globina beta; essa mutação resulta na substituição do ácido glutâmico por glutamina na proteína. É a terceir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::017dc5a931424af5faffbd46dbd61da3
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842003000300007&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842003000300007&lng=en&tlng=en
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
Hemoglobin. 8:353-361
During a screening program for gestational diabetes, hemoglobin D "Los Angeles" (beta 121 Glu----Gln) was detected by HPLC in an overweight but healthy pregnant Austrian woman. The chromatogram of the hemolysate revealed an unusual splitting of the h
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Protein Structure. 188:55-58
Hemoglobin D Los Angeles α 2 β 2 121 Gln was found in three members of a French family. The usual technical procedure was modified to exclude acid pH at all stages. The final Edman degradation demonstrated that the residue in the N-terminal positio
Autor:
Bernadine Brimhall, Rose G. Schneider, Jack B. Alperin, Satoshi Ueda, William C. Levin, Richard T. Jones
Publikováno v:
Blood. 32:250-259
Data are presented on two Caucasian families with hemoglobin D Los Angeles, (α2β2121gln) In one family, the mother, of Spanish origin, has sickle cell trait and the father, of Mexican origin, has hemoglobin D trait. One child has sickle cell hemogl
Publikováno v:
Journal of Pediatric Hematology/Oncology. 10:316-318
Findings are presented on a Pakistani family in Doha, Qatar with hemoglobin D-Los Angeles (alpha 2 beta 3 121 (glutamine----glycine) and thalassemia trait. The propositus, a child, has hemoglobin D-beta(0) thalassemia, and suffers from moderately sev