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A Gal

Showing results (351-360 of 488) with videos related to

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Heredity|October 16, 2008
Population fragmentation leads to isolation by distance but not genetic impoverishment in the philopatric Lesser Kestrel: a comparison with the widespread and sympatric Eurasian KestrelM Alcaide, D Serrano, J J Negro, et al.
Clinical Genetics|March 1, 1996
Jumping translocation in a phenotypically normal femaleC L von Ballestrem, M G Boavida, C Zuther, et al.
Journal of Veterinary Internal Medicine|April 14, 2017
Biological Variability in Serum Cortisol Concentration Post-adrenocorticotropic Hormone Stimulation in Healthy DogsA Gal, K Weidgraaf, J P Bowden, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
The EMBO Journal|December 20, 1984
Reconstitution of beta-adrenergic receptor with components of adenylate cyclaseM Hekman, D Feder, A K Keenan, et al.
Clinical Genetics|January 1, 1989
Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneityA Gal, B Wirth, H Kääriäinen, et al.
Neurology|May 24, 2000
Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239IU Finckh, A Alberici, M Antoniazzi, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1990
Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysisA A Bergen, C Samanns, D B Van Dorp, et al.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Nature|December 18, 2009
A single sub-kilometre Kuiper belt object from a stellar occultation in archival dataH E Schlichting, E O Ofek, M Wenz, et al.
Pageof 49

Showing results (351-360 of 488) with videos related to

Sort By:
Pageof 49
Heredity|October 16, 2008
Population fragmentation leads to isolation by distance but not genetic impoverishment in the philopatric Lesser Kestrel: a comparison with the widespread and sympatric Eurasian KestrelM Alcaide, D Serrano, J J Negro, et al.
Clinical Genetics|March 1, 1996
Jumping translocation in a phenotypically normal femaleC L von Ballestrem, M G Boavida, C Zuther, et al.
Journal of Veterinary Internal Medicine|April 14, 2017
Biological Variability in Serum Cortisol Concentration Post-adrenocorticotropic Hormone Stimulation in Healthy DogsA Gal, K Weidgraaf, J P Bowden, et al.
Journal of Medical Genetics|February 1, 1996
Five novel mutations in the L1CAM gene in families with X linked hydrocephalusS M Gu, U Orth, A Veske, et al.
The EMBO Journal|December 20, 1984
Reconstitution of beta-adrenergic receptor with components of adenylate cyclaseM Hekman, D Feder, A K Keenan, et al.
Clinical Genetics|January 1, 1989
Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneityA Gal, B Wirth, H Kääriäinen, et al.
Neurology|May 24, 2000
Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239IU Finckh, A Alberici, M Antoniazzi, et al.
Ophthalmic Paediatrics and Genetics|September 1, 1990
Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysisA A Bergen, C Samanns, D B Van Dorp, et al.
Nature Genetics|November 4, 2000
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaA Gal, Y Li, D A Thompson, et al.
Nature|December 18, 2009
A single sub-kilometre Kuiper belt object from a stellar occultation in archival dataH E Schlichting, E O Ofek, M Wenz, et al.
Pageof 49