B D Lake - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

B D Lake

Showing results (131-140 of 136) with videos related to

Pageof 14

Sort By:

You have reached the last page of results.This site can display upto 136 results.

Advances in Experimental Medicine and Biology|January 1, 1989

Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinosesD N Palmer, I M Fearnley, S M Medd, et al.

American Journal of Human Genetics|September 16, 1999

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathyS Rahman, J W Taanman, J M Cooper, et al.

The British Journal of Dermatology|May 8, 1999

Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1J A McGrath, P H Hoeger, A M Christiano, et al.

Annals of Neurology|July 1, 1996

Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.

Neurobiology of Disease|October 21, 1999

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.

Human Molecular Genetics|March 21, 1998

Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic depositsH M Mitchison, S L Hofmann, C H Becerra, et al.

Pageof 14

Search research articles

Showing results (131-140 of 136) with videos related to

Sort By:

Pageof 14

You have reached the last page of results.This site can display upto 136 results.

Advances in Experimental Medicine and Biology|January 1, 1989

Lysosomal storage of the DCCD reactive proteolipid subunit of mitochondrial ATP synthase in human and ovine ceroid lipofuscinosesD N Palmer, I M Fearnley, S M Medd, et al.

American Journal of Human Genetics|September 16, 1999

A missense mutation of cytochrome oxidase subunit II causes defective assembly and myopathyS Rahman, J W Taanman, J M Cooper, et al.

The British Journal of Dermatology|May 8, 1999

Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1J A McGrath, P H Hoeger, A M Christiano, et al.

Annals of Neurology|July 1, 1996

Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.

Neurobiology of Disease|October 21, 1999

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.

Human Molecular Genetics|March 21, 1998

Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic depositsH M Mitchison, S L Hofmann, C H Becerra, et al.

Pageof 14