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Mayka Sanchez

Showing results (11-20 of 28) with videos related to

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Human Molecular Genetics|July 14, 2009
Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanismsAndrew J Ramsay, Victor Quesada, Mayka Sanchez, et al.
Hemasphere|October 16, 2020
Control of Systemic Iron Homeostasis by the 3' Iron-Responsive Element of Divalent Metal Transporter 1 in MiceElisabeth Tybl, Hiromi Gunshin, Sanjay Gupta, et al.
Blood|August 5, 2017
The actin-binding protein profilin 2 is a novel regulator of iron homeostasisSara Luscieti, Bruno Galy, Lucia Gutierrez, et al.
International Journal of Molecular Sciences|June 2, 2021
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New CasesFerran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, et al.
Nature Genetics|April 21, 2004
An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in miceCindy N Roy, Angel O Custodio, Jos de Graaf, et al.
Immunobiology|May 24, 2011
Mycobacteria-induced anaemia revisited: a molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidinPedro N Rodrigues, Sandro S Gomes, João V Neves, et al.
Scientific Reports|April 8, 2025
The role of genetic testing in accurate diagnosis of X-linked sideroblastic anemia: novel ALAS2 mutations and the impact of X-chromosome inactivationDaniel Jové-Solavera, Marta Rámila, Xènia Ferrer-Cortés, et al.
Pharmaceuticals (Basel, Switzerland)|January 26, 2019
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New CasesBeatriz Cadenas, Josep Fita-Torró, Mar Bermúdez-Cortés, et al.
Plos One|February 4, 2014
Molecular evolution of multiple-level control of heme biosynthesis pathway in animal kingdomWen-Shyong Tzou, Ying Chu, Tzung-Yi Lin, et al.
Haematologica|March 12, 2011
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemiaCaroline Kannengiesser, Mayka Sanchez, Marion Sweeney, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|July 14, 2009
Matriptase-2 mutations in iron-refractory iron deficiency anemia patients provide new insights into protease activation mechanismsAndrew J Ramsay, Victor Quesada, Mayka Sanchez, et al.
Hemasphere|October 16, 2020
Control of Systemic Iron Homeostasis by the 3' Iron-Responsive Element of Divalent Metal Transporter 1 in MiceElisabeth Tybl, Hiromi Gunshin, Sanjay Gupta, et al.
Blood|August 5, 2017
The actin-binding protein profilin 2 is a novel regulator of iron homeostasisSara Luscieti, Bruno Galy, Lucia Gutierrez, et al.
International Journal of Molecular Sciences|June 2, 2021
Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New CasesFerran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, et al.
Nature Genetics|April 21, 2004
An Hfe-dependent pathway mediates hyposideremia in response to lipopolysaccharide-induced inflammation in miceCindy N Roy, Angel O Custodio, Jos de Graaf, et al.
Immunobiology|May 24, 2011
Mycobacteria-induced anaemia revisited: a molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidinPedro N Rodrigues, Sandro S Gomes, João V Neves, et al.
Scientific Reports|April 8, 2025
The role of genetic testing in accurate diagnosis of X-linked sideroblastic anemia: novel ALAS2 mutations and the impact of X-chromosome inactivationDaniel Jové-Solavera, Marta Rámila, Xènia Ferrer-Cortés, et al.
Pharmaceuticals (Basel, Switzerland)|January 26, 2019
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New CasesBeatriz Cadenas, Josep Fita-Torró, Mar Bermúdez-Cortés, et al.
Plos One|February 4, 2014
Molecular evolution of multiple-level control of heme biosynthesis pathway in animal kingdomWen-Shyong Tzou, Ying Chu, Tzung-Yi Lin, et al.
Haematologica|March 12, 2011
Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemiaCaroline Kannengiesser, Mayka Sanchez, Marion Sweeney, et al.
Pageof 3