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Nucleic Acids Research
|
February 21, 1998
The Androgen Receptor Gene Mutations Database
B Gottlieb, H Lehvaslaiho, L K Beitel, et al.
Human Mutation
|
November 26, 1999
Analysis of exon 1 mutations in the androgen receptor gene
B Gottlieb, D M Vasiliou, R Lumbroso, et al.
Brain Research Bulletin
|
November 24, 2001
Cytochrome c oxidase subunit Vb interacts with human androgen receptor: a potential mechanism for neurotoxicity in spinobulbar muscular atrophy
A M Beauchemin, B Gottlieb, L K Beitel, et al.
Nucleic Acids Research
|
April 25, 1986
Studies on HSAG, a middle repetitive family of genetic elements which elicit a leukemia-related cellular surface antigen
L K Beitel, J W Chamberlain, S Benchimol, et al.
Neurotoxicity Research
|
April 28, 2004
Characterization of intracellular aggregates using fluorescently-tagged polyglutamine-expanded androgen receptor
V Panet-Raymond, B Gottlieb, L K Beitel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 18, 1999
Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively
D L Shkolny, L K Beitel, J Ginsberg, et al.
Breast Cancer Research and Treatment
|
January 5, 2002
The polymorphic CAG repeat of the androgen receptor gene: a potential role in breast cancer in women over 40
Y A Elhaji, B Gottlieb, R Lumbroso, et al.
Molecular Endocrinology (Baltimore, Md.)
|
January 1, 1993
Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes
P Kazemi-Esfarjani, L K Beitel, M Trifiro, et al.
Prostate Cancer and Prostatic Diseases
|
April 19, 2007
Androgen receptor CAG repeat length contraction in diseased and non-diseased prostatic tissues
K Sircar, B Gottlieb, C Alvarado, et al.
The Journal of Pediatrics
|
September 8, 2009
Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype
C M Girardin, C Deal, E Lemyre, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Nucleic Acids Research
|
February 21, 1998
The Androgen Receptor Gene Mutations Database
B Gottlieb, H Lehvaslaiho, L K Beitel, et al.
Human Mutation
|
November 26, 1999
Analysis of exon 1 mutations in the androgen receptor gene
B Gottlieb, D M Vasiliou, R Lumbroso, et al.
Brain Research Bulletin
|
November 24, 2001
Cytochrome c oxidase subunit Vb interacts with human androgen receptor: a potential mechanism for neurotoxicity in spinobulbar muscular atrophy
A M Beauchemin, B Gottlieb, L K Beitel, et al.
Nucleic Acids Research
|
April 25, 1986
Studies on HSAG, a middle repetitive family of genetic elements which elicit a leukemia-related cellular surface antigen
L K Beitel, J W Chamberlain, S Benchimol, et al.
Neurotoxicity Research
|
April 28, 2004
Characterization of intracellular aggregates using fluorescently-tagged polyglutamine-expanded androgen receptor
V Panet-Raymond, B Gottlieb, L K Beitel, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 18, 1999
Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively
D L Shkolny, L K Beitel, J Ginsberg, et al.
Breast Cancer Research and Treatment
|
January 5, 2002
The polymorphic CAG repeat of the androgen receptor gene: a potential role in breast cancer in women over 40
Y A Elhaji, B Gottlieb, R Lumbroso, et al.
Molecular Endocrinology (Baltimore, Md.)
|
January 1, 1993
Substitution of valine-865 by methionine or leucine in the human androgen receptor causes complete or partial androgen insensitivity, respectively with distinct androgen receptor phenotypes
P Kazemi-Esfarjani, L K Beitel, M Trifiro, et al.
Prostate Cancer and Prostatic Diseases
|
April 19, 2007
Androgen receptor CAG repeat length contraction in diseased and non-diseased prostatic tissues
K Sircar, B Gottlieb, C Alvarado, et al.
The Journal of Pediatrics
|
September 8, 2009
Molecular studies of a patient with complete androgen insensitivity and a 47,XXY karyotype
C M Girardin, C Deal, E Lemyre, et al.
Page
of 3