Search research articles
Contact Us
Filters
Showing results (11-20 of 22) with videos related to
Page
of 3
Sort By:
The Journal of Steroid Biochemistry and Molecular Biology
|
March 24, 2017
Attenuation of UVR-induced vitamin D<sub>3</sub> synthesis in a mouse model deleted for keratinocyte lathosterol 5-desaturase
Anastasia M Makarova, Saloni Pasta, Gordon Watson, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
May 2, 2009
Steroid production and excretion by the pregnant mouse, particularly in relation to pregnancies with fetuses deficient in Delta7-sterol reductase (Dhcr7), the enzyme associated with Smith-Lemli-Opitz syndrome
Xavier Matabosch, Mahbuba Rahman, Beverly Hughes, et al.
Steroids
|
January 13, 2004
The implications of 7-dehydrosterol-7-reductase deficiency (Smith-Lemli-Opitz syndrome) to neurosteroid production
Josep Marcos, Li-Wei Guo, William K Wilson, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 13, 2002
Identification of 7(8) and 8(9) unsaturated adrenal steroid metabolites produced by patients with 7-dehydrosterol-delta7-reductase deficiency (Smith-Lemli-Opitz syndrome)
Cedric Shackleton, Esther Roitman, Li Wei Guo, et al.
The Journal of Investigative Dermatology
|
February 14, 2002
Gas chromatography/mass spectrometry characterization of corticosteroid metabolism in human immortalized keratinocytes
Andrzej Slominski, Jacobo Wortsman, Mark F Foecking, et al.
Clinical Chemistry
|
June 17, 2008
Potential of sterol analysis by liquid chromatography-tandem mass spectrometry for the prenatal diagnosis of Smith-Lemli-Opitz syndrome
William J Griffiths, Yuqin Wang, Kersti Karu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 29, 2008
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism
David S Geller, Junhui Zhang, Max V Wisgerhof, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
August 31, 2010
Increasing cholesterol synthesis in 7-dehydrosterol reductase (DHCR7) deficient mouse models through gene transfer
Xavier Matabosch, Lee Ying, Montserrat Serra, et al.
Journal of Molecular Endocrinology
|
February 21, 2018
SULFATION PATHWAYS: Alternate steroid sulfation pathways targeted by LC-MS/MS analysis of disulfates: application to prenatal diagnosis of steroid synthesis disorders
Oscar J Pozo, Josep Marcos, Olha Khymenets, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Mutations in CYP11B1 gene: phenotype-genotype correlations
Yuan-Shan Zhu, Juan J Cordero, Selcuk Can, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
The Journal of Steroid Biochemistry and Molecular Biology
|
March 24, 2017
Attenuation of UVR-induced vitamin D<sub>3</sub> synthesis in a mouse model deleted for keratinocyte lathosterol 5-desaturase
Anastasia M Makarova, Saloni Pasta, Gordon Watson, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
May 2, 2009
Steroid production and excretion by the pregnant mouse, particularly in relation to pregnancies with fetuses deficient in Delta7-sterol reductase (Dhcr7), the enzyme associated with Smith-Lemli-Opitz syndrome
Xavier Matabosch, Mahbuba Rahman, Beverly Hughes, et al.
Steroids
|
January 13, 2004
The implications of 7-dehydrosterol-7-reductase deficiency (Smith-Lemli-Opitz syndrome) to neurosteroid production
Josep Marcos, Li-Wei Guo, William K Wilson, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
December 13, 2002
Identification of 7(8) and 8(9) unsaturated adrenal steroid metabolites produced by patients with 7-dehydrosterol-delta7-reductase deficiency (Smith-Lemli-Opitz syndrome)
Cedric Shackleton, Esther Roitman, Li Wei Guo, et al.
The Journal of Investigative Dermatology
|
February 14, 2002
Gas chromatography/mass spectrometry characterization of corticosteroid metabolism in human immortalized keratinocytes
Andrzej Slominski, Jacobo Wortsman, Mark F Foecking, et al.
Clinical Chemistry
|
June 17, 2008
Potential of sterol analysis by liquid chromatography-tandem mass spectrometry for the prenatal diagnosis of Smith-Lemli-Opitz syndrome
William J Griffiths, Yuqin Wang, Kersti Karu, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 29, 2008
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism
David S Geller, Junhui Zhang, Max V Wisgerhof, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
August 31, 2010
Increasing cholesterol synthesis in 7-dehydrosterol reductase (DHCR7) deficient mouse models through gene transfer
Xavier Matabosch, Lee Ying, Montserrat Serra, et al.
Journal of Molecular Endocrinology
|
February 21, 2018
SULFATION PATHWAYS: Alternate steroid sulfation pathways targeted by LC-MS/MS analysis of disulfates: application to prenatal diagnosis of steroid synthesis disorders
Oscar J Pozo, Josep Marcos, Olha Khymenets, et al.
American Journal of Medical Genetics. Part A
|
September 11, 2003
Mutations in CYP11B1 gene: phenotype-genotype correlations
Yuan-Shan Zhu, Juan J Cordero, Selcuk Can, et al.
Page
of 3