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B D Lake

Showing results (121-130 of 136) with videos related to

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Brain : a Journal of Neurology|February 25, 2000
Cytochrome oxidase immunohistochemistry: clues for genetic mechanismsS Rahman, B D Lake, J W Taanman, et al.
Molecular Genetics and Metabolism|April 7, 1999
A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7R B Wheeler, J D Sharp, W A Mitchell, et al.
Human Molecular Genetics|April 1, 1997
Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23J D Sharp, R B Wheeler, B D Lake, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
American Journal of Medical Genetics|February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)D N Palmer, I M Fearnley, J E Walker, et al.
The British Journal of Dermatology|April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus samplingJ A McGrath, M G Dunnill, A M Christiano, et al.
Journal of Hepatology|May 5, 1998
Liver failure associated with mitochondrial DNA depletionA A Morris, J W Taanman, J Blake, et al.
The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidationP T Clayton, B D Lake, M Hjelm, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Pageof 14

Showing results (121-130 of 136) with videos related to

Sort By:
Pageof 14
Brain : a Journal of Neurology|February 25, 2000
Cytochrome oxidase immunohistochemistry: clues for genetic mechanismsS Rahman, B D Lake, J W Taanman, et al.
Molecular Genetics and Metabolism|April 7, 1999
A new locus for variant late infantile neuronal ceroid lipofuscinosis-CLN7R B Wheeler, J D Sharp, W A Mitchell, et al.
Human Molecular Genetics|April 1, 1997
Loci for classical and a variant late infantile neuronal ceroid lipofuscinosis map to chromosomes 11p15 and 15q21-23J D Sharp, R B Wheeler, B D Lake, et al.
Journal of Medical Genetics|September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosaM G Dunnill, C H Rodeck, A J Richards, et al.
American Journal of Medical Genetics|February 15, 1992
Mitochondrial ATP synthase subunit c storage in the ceroid-lipofuscinoses (Batten disease)D N Palmer, I M Fearnley, J E Walker, et al.
The British Journal of Dermatology|April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus samplingJ A McGrath, M G Dunnill, A M Christiano, et al.
Journal of Hepatology|May 5, 1998
Liver failure associated with mitochondrial DNA depletionA A Morris, J W Taanman, J Blake, et al.
The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidationP T Clayton, B D Lake, M Hjelm, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Pageof 14