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K Mistry

Showing results (191-200 of 237) with videos related to

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American Journal of Physiology. Gastrointestinal and Liver Physiology|May 27, 2010
Protease activation during in vivo pancreatitis is dependent on calcineurin activationAhsan U Shah, Amna Sarwar, Abrahim I Orabi, et al.
Journal of Molecular and Cellular Cardiology|December 3, 2014
Redox regulation of cardiomyocyte cell cycling via an ERK1/2 and c-Myc-dependent activation of cyclin D2 transcriptionThomas V A Murray, Ioannis Smyrnias, Moritz Schnelle, et al.
Shock (Augusta, Ga.)|March 10, 2001
Alterations in arginine metabolic enzymes in traumaA C Bernard, S K Mistry, S M Morris, et al.
Orphanet Journal of Rare Diseases|April 4, 2022
Transformative effect of a Humanitarian Program for individuals affected by rare diseases: building support systems and creating local expertiseI C Verma, A El-Beshlawy, A Tylki-Szymańska, et al.
American Journal of Hematology|March 6, 2012
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variationClarence K Zhang, Philip B Stein, Jun Liu, et al.
Nucleic Acids Research|November 30, 2017
Oxygen gradients can determine epigenetic asymmetry and cellular differentiation via differential regulation of Tet activity in embryonic stem cellsSimon Burr, Anna Caldwell, Mei Chong, et al.
Biochemistry|March 22, 2001
Probing erectile function: S-(2-boronoethyl)-L-cysteine binds to arginase as a transition state analogue and enhances smooth muscle relaxation in human penile corpus cavernosumN N Kim, J D Cox, R F Baggio, et al.
Molecular Genetics and Metabolism Reports|November 25, 2021
Long-read single molecule real-time (SMRT) sequencing of GBA1 locus in Gaucher disease national cohort from Argentina reveals high frequency of complex allele underlying severe skeletal phenotypes: Collaborative study from the Argentine Group for Diagnosis and Treatment of Gaucher DiseaseGuillermo I Drelichman, Nicolas Fernández Escobar, Barbara C Soberon, et al.
Stem Cells (Dayton, Ohio)|October 21, 2006
Cells isolated from umbilical cord tissue rescue photoreceptors and visual functions in a rodent model of retinal diseaseRaymond D Lund, Shaomei Wang, Bin Lu, et al.
Hepatology Communications|January 8, 2025
Acid sphingomyelinase deficiency and Gaucher disease: Underdiagnosed and often treatable causes of hepatomegaly, splenomegaly, and low HDL cholesterol in lean individualsPramod K Mistry, David Cassiman, Simon A Jones, et al.
Pageof 24

Showing results (191-200 of 237) with videos related to

Sort By:
Pageof 24
American Journal of Physiology. Gastrointestinal and Liver Physiology|May 27, 2010
Protease activation during in vivo pancreatitis is dependent on calcineurin activationAhsan U Shah, Amna Sarwar, Abrahim I Orabi, et al.
Journal of Molecular and Cellular Cardiology|December 3, 2014
Redox regulation of cardiomyocyte cell cycling via an ERK1/2 and c-Myc-dependent activation of cyclin D2 transcriptionThomas V A Murray, Ioannis Smyrnias, Moritz Schnelle, et al.
Shock (Augusta, Ga.)|March 10, 2001
Alterations in arginine metabolic enzymes in traumaA C Bernard, S K Mistry, S M Morris, et al.
Orphanet Journal of Rare Diseases|April 4, 2022
Transformative effect of a Humanitarian Program for individuals affected by rare diseases: building support systems and creating local expertiseI C Verma, A El-Beshlawy, A Tylki-Szymańska, et al.
American Journal of Hematology|March 6, 2012
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variationClarence K Zhang, Philip B Stein, Jun Liu, et al.
Nucleic Acids Research|November 30, 2017
Oxygen gradients can determine epigenetic asymmetry and cellular differentiation via differential regulation of Tet activity in embryonic stem cellsSimon Burr, Anna Caldwell, Mei Chong, et al.
Biochemistry|March 22, 2001
Probing erectile function: S-(2-boronoethyl)-L-cysteine binds to arginase as a transition state analogue and enhances smooth muscle relaxation in human penile corpus cavernosumN N Kim, J D Cox, R F Baggio, et al.
Molecular Genetics and Metabolism Reports|November 25, 2021
Long-read single molecule real-time (SMRT) sequencing of GBA1 locus in Gaucher disease national cohort from Argentina reveals high frequency of complex allele underlying severe skeletal phenotypes: Collaborative study from the Argentine Group for Diagnosis and Treatment of Gaucher DiseaseGuillermo I Drelichman, Nicolas Fernández Escobar, Barbara C Soberon, et al.
Stem Cells (Dayton, Ohio)|October 21, 2006
Cells isolated from umbilical cord tissue rescue photoreceptors and visual functions in a rodent model of retinal diseaseRaymond D Lund, Shaomei Wang, Bin Lu, et al.
Hepatology Communications|January 8, 2025
Acid sphingomyelinase deficiency and Gaucher disease: Underdiagnosed and often treatable causes of hepatomegaly, splenomegaly, and low HDL cholesterol in lean individualsPramod K Mistry, David Cassiman, Simon A Jones, et al.
Pageof 24