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International Journal of Molecular Sciences
|
December 10, 2021
Drug Repurposing in Rare Diseases: An Integrative Study of Drug Screening and Transcriptomic Analysis in Nephropathic Cystinosis
Francesco Bellomo, Ester De Leo, Anna Taranta, et al.
The Journal of Biological Chemistry
|
October 1, 2005
Nitrosylation of human glutathione transferase P1-1 with dinitrosyl diglutathionyl iron complex in vitro and in vivo
Eleonora Cesareo, Lorien J Parker, Jens Z Pedersen, et al.
Amino Acids
|
October 11, 2011
Erythrocyte glutathione transferase: a potential new biomarker in chronic kidney diseases which correlates with plasma homocysteine
Mariarita Dessì, Annalisa Noce, Kutayba F Dawood, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 30, 2011
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children
Alessandra Terracciano, Florence Renaldo, Ginevra Zanni, et al.
Kidney International
|
March 21, 2016
Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cells
Laura R Rega, Elena Polishchuk, Sandro Montefusco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2019
Detection of iron deficiency in children with Down syndrome
Sarah J Hart, Kanecia Zimmerman, Corinne M Linardic, et al.
Journal of the American Society of Nephrology : JASN
|
September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement
Francesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Molecular Genetics and Metabolism
|
September 27, 2012
EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome
Diego Martinelli, Michela Catteruccia, Fiorella Piemonte, et al.
Obesity Surgery
|
September 21, 2021
Changes in Total Homocysteine and Glutathione Levels After Laparoscopic Sleeve Gastrectomy in Children with Metabolic-Associated Fatty Liver Disease
Anna Pastore, Nadia Panera, Antonella Mosca, et al.
Scientific Reports
|
February 16, 2017
Cystinosis (ctns) zebrafish mutant shows pronephric glomerular and tubular dysfunction
Mohamed A Elmonem, Ramzi Khalil, Ladan Khodaparast, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 87) with videos related to
Sort By:
Page
of 9
International Journal of Molecular Sciences
|
December 10, 2021
Drug Repurposing in Rare Diseases: An Integrative Study of Drug Screening and Transcriptomic Analysis in Nephropathic Cystinosis
Francesco Bellomo, Ester De Leo, Anna Taranta, et al.
The Journal of Biological Chemistry
|
October 1, 2005
Nitrosylation of human glutathione transferase P1-1 with dinitrosyl diglutathionyl iron complex in vitro and in vivo
Eleonora Cesareo, Lorien J Parker, Jens Z Pedersen, et al.
Amino Acids
|
October 11, 2011
Erythrocyte glutathione transferase: a potential new biomarker in chronic kidney diseases which correlates with plasma homocysteine
Mariarita Dessì, Annalisa Noce, Kutayba F Dawood, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
August 30, 2011
The use of muscle biopsy in the diagnosis of undefined ataxia with cerebellar atrophy in children
Alessandra Terracciano, Florence Renaldo, Ginevra Zanni, et al.
Kidney International
|
March 21, 2016
Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cells
Laura R Rega, Elena Polishchuk, Sandro Montefusco, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 17, 2019
Detection of iron deficiency in children with Down syndrome
Sarah J Hart, Kanecia Zimmerman, Corinne M Linardic, et al.
Journal of the American Society of Nephrology : JASN
|
September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement
Francesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Molecular Genetics and Metabolism
|
September 27, 2012
EPI-743 reverses the progression of the pediatric mitochondrial disease--genetically defined Leigh Syndrome
Diego Martinelli, Michela Catteruccia, Fiorella Piemonte, et al.
Obesity Surgery
|
September 21, 2021
Changes in Total Homocysteine and Glutathione Levels After Laparoscopic Sleeve Gastrectomy in Children with Metabolic-Associated Fatty Liver Disease
Anna Pastore, Nadia Panera, Antonella Mosca, et al.
Scientific Reports
|
February 16, 2017
Cystinosis (ctns) zebrafish mutant shows pronephric glomerular and tubular dysfunction
Mohamed A Elmonem, Ramzi Khalil, Ladan Khodaparast, et al.
Page
of 9