Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Red cell disorder"'
Autor:
Paulo Augusto Achucarro Silveira, Fernando Ferreira Costa, Jhonathan Angel Araujo Fernandez, Silvia Regina Brandalise, Ana Paula Hitomi Yokoyama, Sara Teresinha Olalla Saad, Maria Carolina Costa Melo Svidnicki, Andrey Santos, Isis Q. Magalhães, Vitória Régia Pereira Pinheiro
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 40, Iss 1, Pp 5-11 (2018)
Hematology, Transfusion and Cell Therapy, Volume: 40, Issue: 1, Pages: 11-5, Published: MAR 2018
Hematology, Transfusion and Cell Therapy, Volume: 40, Issue: 1, Pages: 11-5, Published: MAR 2018
Background: Pyruvate kinase deficiency is a hereditary disease that affects the glycolytic pathway of the red blood cell, causing nonspherocytic hemolytic anemia. The disease is transmitted as an autosomal recessive trait and shows a marked variabili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a957079edc35789245d40a437c032856
http://www.sciencedirect.com/science/article/pii/S1516848417301305
http://www.sciencedirect.com/science/article/pii/S1516848417301305
Autor:
S. Paci, Ilaria Capolsini, Selin Aytac, Anna Zaninoni, Paola Bianchi, Elisa Fermo, Mualla Cetin, Alberto Zanella, Wilma Barcellini, Anna Paola Marcello, Cristina Vercellati, Maddalena Casale
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology, Vol 10 (2019)
Glucose-6-phosphate isomerase (GPI, EC 5.3.1.9) is a dimeric enzyme that catalyzes the reversible isomerization of glucose-6-phosphate to fructose-6-phosphate, the second reaction step of glycolysis. GPI deficiency, transmitted as an autosomal recess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f467e0c4192f504e3456707265a57f
https://pubmed.ncbi.nlm.nih.gov/31133865
https://pubmed.ncbi.nlm.nih.gov/31133865
Akademický článek
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