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J Michaud

Showing results (181-190 of 206) with videos related to

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Entropy (Basel, Switzerland)|January 8, 2025
Opening the AI Black Box: Distilling Machine-Learned Algorithms into CodeEric J Michaud, Isaac Liao, Vedang Lad, et al.
Genetics|September 16, 2008
A targeted deleterious allele of the splicing factor SCNM1 in the mouseViive M Howell, Georgius de Haan, Sarah Bergren, et al.
The American Journal of Pathology|June 1, 1997
Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesionB K Yoder, W G Richards, C Sommardahl, et al.
Kidney International|October 1, 1996
Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNAB K Yoder, W G Richards, C Sommardahl, et al.
The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.
Annals of Neurology|October 1, 1988
Encephalitis among Cree children in northern QuebecD N Black, G V Watters, E Andermann, et al.
Neurorehabilitation|February 15, 2014
Rehabilitation of children with brain tumorsL J Michaud, S R Ried, J Radcliffe, et al.
The Journal of Endocrinology|January 1, 1998
Role of the agouti gene in obesityE J Michaud, R L Mynatt, R J Miltenberger, et al.
American Journal of Human Genetics|March 1, 1995
Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226VJ Michaud, G N Thompson, L C Brody, et al.
Annals of Neurology|March 11, 1999
Stroke-like episodes in autosomal recessive cytochrome oxidase deficiencyC Morin, J Dubé, B H Robinson, et al.
Pageof 21

Showing results (181-190 of 206) with videos related to

Sort By:
Pageof 21
Entropy (Basel, Switzerland)|January 8, 2025
Opening the AI Black Box: Distilling Machine-Learned Algorithms into CodeEric J Michaud, Isaac Liao, Vedang Lad, et al.
Genetics|September 16, 2008
A targeted deleterious allele of the splicing factor SCNM1 in the mouseViive M Howell, Georgius de Haan, Sarah Bergren, et al.
The American Journal of Pathology|June 1, 1997
Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant. A new model to study the liver lesionB K Yoder, W G Richards, C Sommardahl, et al.
Kidney International|October 1, 1996
Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNAB K Yoder, W G Richards, C Sommardahl, et al.
The Journal of Biological Chemistry|February 15, 1992
Ornithine delta-aminotransferase mutations in gyrate atrophy. Allelic heterogeneity and functional consequencesL C Brody, G A Mitchell, C Obie, et al.
Annals of Neurology|October 1, 1988
Encephalitis among Cree children in northern QuebecD N Black, G V Watters, E Andermann, et al.
Neurorehabilitation|February 15, 2014
Rehabilitation of children with brain tumorsL J Michaud, S R Ried, J Radcliffe, et al.
The Journal of Endocrinology|January 1, 1998
Role of the agouti gene in obesityE J Michaud, R L Mynatt, R J Miltenberger, et al.
American Journal of Human Genetics|March 1, 1995
Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226VJ Michaud, G N Thompson, L C Brody, et al.
Annals of Neurology|March 11, 1999
Stroke-like episodes in autosomal recessive cytochrome oxidase deficiencyC Morin, J Dubé, B H Robinson, et al.
Pageof 21