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Alfredo Santana

Research Profile

Disorders

Chemicals & Drugs

Living Beings

Devices

Gene Transfer Techniques

Procedures

Anatomy

Phenomena

Founder Effect

Physiology

Liver Regeneration

Occupations

Molecular Biology

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Publications

TOP 3
Eduardo Salido; Marisol Rodriguez-Pena; Alfredo Santana; Stuart G Beattie; Harald Petry; Armando Torres
Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer.
Eduardo Salido; Xiao M Li; Yang Lu; Xia Wang; Alfredo Santana; Namita Roy-Chowdhury; Armando Torres; Lawrence J Shapiro; Jayanta Roy-Chowdhury
Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.
Chandan Guha; Kosho Yamanouchi; Jinlan Jiang; Xia Wang; Namita Roy-Chowdhury; Alfredo Santana; Lawrence J Shapiro; Eduardo Salido; Jayanta Roy-Chowdhury
Feasibility of hepatocyte transplantation-based therapies for primary hyperoxalurias.

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All Publications

2011: Eduardo Salido; Marisol Rodriguez-Pena; Alfredo Santana; Stuart G Beattie; Harald Petry; Armando Torres
Phenotypic correction of a mouse model for primary hyperoxaluria with adeno-associated virus gene transfer.
Molecular therapy : the journal of the American Society of Gene Therapy 2011;19(5):870-5.
2006: Eduardo Salido; Xiao M Li; Yang Lu; Xia Wang; Alfredo Santana; Namita Roy-Chowdhury; Armando Torres; Lawrence J Shapiro; Jayanta Roy-Chowdhury
Alanine-glyoxylate aminotransferase-deficient mice, a model for primary hyperoxaluria that responds to adenoviral gene transfer.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(48):18249-54.
2005: Chandan Guha; Kosho Yamanouchi; Jinlan Jiang; Xia Wang; Namita Roy-Chowdhury; Alfredo Santana; Lawrence J Shapiro; Eduardo Salido; Jayanta Roy-Chowdhury
Feasibility of hepatocyte transplantation-based therapies for primary hyperoxalurias.
American journal of nephrology 2005;25(2):161-70.
2003: Alfredo Santana; Eduardo Salido; Armando Torres; Lawrence J Shapiro
Primary hyperoxaluria type 1 in the Canary Islands: a conformational disease due to I244T mutation in the P11L-containing alanine:glyoxylate aminotransferase.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(12):7277-82.
2003: Alfredo Santana; Armando Torres; Eduardo Salido
[Molecular pathology of primary hyperoxaluria].
Nefrología : publicación oficial de la Sociedad Española Nefrologia 2003;23 Suppl 1():90-7.

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Copyright © 2011 Elsevier Inc. All rights reserved.