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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Robert A White

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Blood Cells, Molecules & Diseases|May 5, 2009

Hematologic characterization and chromosomal localization of the novel dominantly inherited mouse hemolytic anemia, neonatal anemia (Nan)Robert A White, Inna V Sokolovsky, Margaret I Britt, et al.

Neuromuscular Disorders : NMD|February 21, 2006

Improvement in survival and muscle function in an mdx/utrn(-/-) double mutant mouse using a human retinal dystrophin transgeneRoger Gaedigk, Douglas J Law, Kathleen M Fitzgerald-Gustafson, et al.

Genomics|August 10, 2010

Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse modelDaniel P Heruth, Troy Hawkins, Derek P Logsdon, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Blood Cells, Molecules & Diseases|May 5, 2009

Hematologic characterization and chromosomal localization of the novel dominantly inherited mouse hemolytic anemia, neonatal anemia (Nan)Robert A White, Inna V Sokolovsky, Margaret I Britt, et al.

Neuromuscular Disorders : NMD|February 21, 2006

Improvement in survival and muscle function in an mdx/utrn(-/-) double mutant mouse using a human retinal dystrophin transgeneRoger Gaedigk, Douglas J Law, Kathleen M Fitzgerald-Gustafson, et al.

Genomics|August 10, 2010

Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse modelDaniel P Heruth, Troy Hawkins, Derek P Logsdon, et al.

Pageof 2