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The EMBO Journal|July 17, 1995

vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain proteinF Jiménez, L E Martin-Morris, L Velasco, et al.

Genomics|May 1, 1993

Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeatA A Lev, D R Rosen, C Kos, et al.

Techniques in Coloproctology|January 23, 2025

Margin matters: analyzing the impact of circumferential margin involvement on survival and recurrence after incomplete total mesorectal excision for rectal cancerA Alipouriani, F Almadi, D R Rosen, et al.

Human Molecular Genetics|November 5, 1999

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formationG Sjöberg, C A Saavedra-Matiz, D R Rosen, et al.

Neurology|June 13, 2001

An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegiaJ J Higgins, J M Loveless, S Goswami, et al.

Neuromuscular Disorders : NMD|September 1, 1995

Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosisP C Sapp, D R Rosen, B A Hosler, et al.

Nature|March 4, 1993

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.

American Journal of Medical Genetics|May 15, 1994

Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markersD R Rosen, P Sapp, J O'Regan, et al.

Human Molecular Genetics|June 1, 1994

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosisD R Rosen, A C Bowling, D Patterson, et al.

Human Genetics|November 1, 1994

Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21P Gregor, S M Gaston, X Yang, et al.

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

Sort By:

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You have reached the last page of results.This site can display upto 20 results.

The EMBO Journal|July 17, 1995

vnd, a gene required for early neurogenesis of Drosophila, encodes a homeodomain proteinF Jiménez, L E Martin-Morris, L Velasco, et al.

Genomics|May 1, 1993

Human ciliary neurotrophic factor: localization to the proximal region of the long arm of chromosome 11 and association with CA/GT dinucleotide repeatA A Lev, D R Rosen, C Kos, et al.

Techniques in Coloproctology|January 23, 2025

Margin matters: analyzing the impact of circumferential margin involvement on survival and recurrence after incomplete total mesorectal excision for rectal cancerA Alipouriani, F Almadi, D R Rosen, et al.

Human Molecular Genetics|November 5, 1999

A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formationG Sjöberg, C A Saavedra-Matiz, D R Rosen, et al.

Neurology|June 13, 2001

An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegiaJ J Higgins, J M Loveless, S Goswami, et al.

Neuromuscular Disorders : NMD|September 1, 1995

Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosisP C Sapp, D R Rosen, B A Hosler, et al.

Nature|March 4, 1993

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.

American Journal of Medical Genetics|May 15, 1994

Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markersD R Rosen, P Sapp, J O'Regan, et al.

Human Molecular Genetics|June 1, 1994

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosisD R Rosen, A C Bowling, D Patterson, et al.

Human Genetics|November 1, 1994

Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21P Gregor, S M Gaston, X Yang, et al.

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