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Translational Psychiatry
|
March 2, 2016
The functional serotonin 1a receptor promoter polymorphism, rs6295, is associated with psychiatric illness and differences in transcription
Z R Donaldson, B le Francois, T L Santos, et al.
Integrative and Comparative Biology
|
July 23, 2015
Fishing for Effective Conservation: Context and Biotic Variation are Keys to Understanding the Survival of Pacific Salmon after Catch-and-Release
Graham D Raby, Michael R Donaldson, Scott G Hinch, et al.
The Review of Scientific Instruments
|
March 2, 2020
Inferred UV fluence focal-spot profiles from soft x-ray pinhole-camera measurements on OMEGA
W Theobald, C Sorce, W R Donaldson, et al.
Physiological and Biochemical Zoology : PBZ
|
April 7, 2010
Physiological condition differentially affects the behavior and survival of two populations of sockeye salmon during their freshwater spawning migration
M R Donaldson, S G Hinch, D A Patterson, et al.
Genomics
|
November 10, 2004
Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens
P Taillon-Miller, S F Saccone, N L Saccone, et al.
Neurology
|
June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
M R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Biorxiv : the Preprint Server for Biology
|
March 27, 2026
Single-library chromosome-scale diploid assemblies of vole genomes resolve a species-specific duplication implicated in pair bonding
Mohamed Abuelanin, Gulhan Kaya, Juniper A Lake, et al.
Cell
|
January 16, 2010
Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis
Devon P Ryan, Magnus R Dias da Silva, Tuck Wah Soong, et al.
Translational Psychiatry
|
April 12, 2017
Animal models to improve our understanding and treatment of suicidal behavior
T D Gould, P Georgiou, L A Brenner, et al.
Cell
|
May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
N M Plaster, R Tawil, M Tristani-Firouzi, et al.
Page
of 34
Search research articles
Search
Showing results (321-330 of 335) with videos related to
Sort By:
Page
of 34
Translational Psychiatry
|
March 2, 2016
The functional serotonin 1a receptor promoter polymorphism, rs6295, is associated with psychiatric illness and differences in transcription
Z R Donaldson, B le Francois, T L Santos, et al.
Integrative and Comparative Biology
|
July 23, 2015
Fishing for Effective Conservation: Context and Biotic Variation are Keys to Understanding the Survival of Pacific Salmon after Catch-and-Release
Graham D Raby, Michael R Donaldson, Scott G Hinch, et al.
The Review of Scientific Instruments
|
March 2, 2020
Inferred UV fluence focal-spot profiles from soft x-ray pinhole-camera measurements on OMEGA
W Theobald, C Sorce, W R Donaldson, et al.
Physiological and Biochemical Zoology : PBZ
|
April 7, 2010
Physiological condition differentially affects the behavior and survival of two populations of sockeye salmon during their freshwater spawning migration
M R Donaldson, S G Hinch, D A Patterson, et al.
Genomics
|
November 10, 2004
Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens
P Taillon-Miller, S F Saccone, N L Saccone, et al.
Neurology
|
June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome
M R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Biorxiv : the Preprint Server for Biology
|
March 27, 2026
Single-library chromosome-scale diploid assemblies of vole genomes resolve a species-specific duplication implicated in pair bonding
Mohamed Abuelanin, Gulhan Kaya, Juniper A Lake, et al.
Cell
|
January 16, 2010
Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis
Devon P Ryan, Magnus R Dias da Silva, Tuck Wah Soong, et al.
Translational Psychiatry
|
April 12, 2017
Animal models to improve our understanding and treatment of suicidal behavior
T D Gould, P Georgiou, L A Brenner, et al.
Cell
|
May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
N M Plaster, R Tawil, M Tristani-Firouzi, et al.
Page
of 34