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Biochemical and Biophysical Research Communications
|
April 1, 2008
An N-ethyl-N-nitrosourea-induced mutation in N-acetyltransferase 1 in mice
Robert P Erickson, Charlene A McQueen, Binh Chau, et al.
Molecular Neuropsychiatry
|
November 4, 2015
Association Study of Genotype by Depressive Response during Tryptophan Depletion in Subjects Recovered from Major Depression
Francisco A Moreno, Robert P Erickson, Holly A Garriock, et al.
European Journal of Pharmacology
|
April 11, 2009
Experimental non-alcoholic fatty liver disease results in decreased hepatic uptake transporter expression and function in rats
Craig D Fisher, Andrew J Lickteig, Lisa M Augustine, et al.
Journal of Applied Genetics
|
November 4, 2004
Tamoxifen and vitamin E treatments delay symptoms in the mouse model of Niemann-Pick C
Eric C Bascuñan-Castillo, Robert P Erickson, Christy M Howison, et al.
Biological Psychology
|
December 23, 2009
Polymorphisms of the HTR1a allele are linked to frontal brain electrical asymmetry
Andrew W Bismark, Francisco A Moreno, Jennifer L Stewart, et al.
Molecular Reproduction and Development
|
December 29, 2007
Confirmation of the role of N-acetyltransferase 2 in teratogen-induced cleft palate using transgenics and knockouts
Robert P Erickson, Wen Cao, Diana K Acuña, et al.
Journal of Neuroscience Research
|
November 8, 2005
Allopregnanolone treatment, both as a single injection or repetitively, delays demyelination and enhances survival of Niemann-Pick C mice
Iram Ahmad, Silvia Lope-Piedrafita, Xiaoning Bi, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2007
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA
Zöe Powis, Sung-Hae L Kang, M Lance Cooper, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Behavioral and Brain Functions : BBF
|
July 11, 2006
Number of risk genotypes is a risk factor for major depressive disorder: a case control study
Holly A Garriock, Pedro Delgado, Mitchel A Kling, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 113) with videos related to
Sort By:
Page
of 12
Biochemical and Biophysical Research Communications
|
April 1, 2008
An N-ethyl-N-nitrosourea-induced mutation in N-acetyltransferase 1 in mice
Robert P Erickson, Charlene A McQueen, Binh Chau, et al.
Molecular Neuropsychiatry
|
November 4, 2015
Association Study of Genotype by Depressive Response during Tryptophan Depletion in Subjects Recovered from Major Depression
Francisco A Moreno, Robert P Erickson, Holly A Garriock, et al.
European Journal of Pharmacology
|
April 11, 2009
Experimental non-alcoholic fatty liver disease results in decreased hepatic uptake transporter expression and function in rats
Craig D Fisher, Andrew J Lickteig, Lisa M Augustine, et al.
Journal of Applied Genetics
|
November 4, 2004
Tamoxifen and vitamin E treatments delay symptoms in the mouse model of Niemann-Pick C
Eric C Bascuñan-Castillo, Robert P Erickson, Christy M Howison, et al.
Biological Psychology
|
December 23, 2009
Polymorphisms of the HTR1a allele are linked to frontal brain electrical asymmetry
Andrew W Bismark, Francisco A Moreno, Jennifer L Stewart, et al.
Molecular Reproduction and Development
|
December 29, 2007
Confirmation of the role of N-acetyltransferase 2 in teratogen-induced cleft palate using transgenics and knockouts
Robert P Erickson, Wen Cao, Diana K Acuña, et al.
Journal of Neuroscience Research
|
November 8, 2005
Allopregnanolone treatment, both as a single injection or repetitively, delays demyelination and enhances survival of Niemann-Pick C mice
Iram Ahmad, Silvia Lope-Piedrafita, Xiaoning Bi, et al.
American Journal of Medical Genetics. Part A
|
November 15, 2007
Mosaic tetrasomy 12p with triplication of 12p detected by array-based comparative genomic hybridization of peripheral blood DNA
Zöe Powis, Sung-Hae L Kang, M Lance Cooper, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Behavioral and Brain Functions : BBF
|
July 11, 2006
Number of risk genotypes is a risk factor for major depressive disorder: a case control study
Holly A Garriock, Pedro Delgado, Mitchel A Kling, et al.
Page
of 12