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Annals of the New York Academy of Sciences
|
August 21, 2015
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance
Ahmed Khattab, Tony Yuen, Sultan Al-Malki, et al.
Pituitary
|
August 3, 2024
Neuroendocrinology of bone
Se-Min Kim, Farhath Sultana, Funda Korkmaz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Maria I New, Moolamannil Abraham, Brian Gonzalez, et al.
The Journal of Clinical Investigation
|
September 22, 2012
Hyperthyroid-associated osteoporosis is exacerbated by the loss of TSH signaling
Ramkumarie Baliram, Li Sun, Jay Cao, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 3, 2003
Transcriptome fingerprints distinguish hallucinogenic and nonhallucinogenic 5-hydroxytryptamine 2A receptor agonist effects in mouse somatosensory cortex
Javier González-Maeso, Tony Yuen, Barbara J Ebersole, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 28, 2021
Thyrotropin, Hyperthyroidism, and Bone Mass
Se-Min Kim, Vitaly Ryu, Sari Miyashita, et al.
Journal of Virology
|
June 16, 2006
Influenza virus evades innate and adaptive immunity via the NS1 protein
Ana Fernandez-Sesma, Svetlana Marukian, Barbara J Ebersole, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 8, 2019
Cytochrome c oxidase dysfunction enhances phagocytic function and osteoclast formation in macrophages
Rajesh Angireddy, Hasan Raza Kazmi, Satish Srinivasan, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 5, 2016
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia
Katja K Dumic, Zorana Grubic, Tony Yuen, et al.
Frontiers in Endocrinology
|
April 4, 2019
FSH Beyond Fertility
Daria Lizneva, Alina Rahimova, Se-Min Kim, et al.
Page
of 12
Search research articles
Search
Showing results (41-50 of 113) with videos related to
Sort By:
Page
of 12
Annals of the New York Academy of Sciences
|
August 21, 2015
A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance
Ahmed Khattab, Tony Yuen, Sultan Al-Malki, et al.
Pituitary
|
August 3, 2024
Neuroendocrinology of bone
Se-Min Kim, Farhath Sultana, Funda Korkmaz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Maria I New, Moolamannil Abraham, Brian Gonzalez, et al.
The Journal of Clinical Investigation
|
September 22, 2012
Hyperthyroid-associated osteoporosis is exacerbated by the loss of TSH signaling
Ramkumarie Baliram, Li Sun, Jay Cao, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 3, 2003
Transcriptome fingerprints distinguish hallucinogenic and nonhallucinogenic 5-hydroxytryptamine 2A receptor agonist effects in mouse somatosensory cortex
Javier González-Maeso, Tony Yuen, Barbara J Ebersole, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 28, 2021
Thyrotropin, Hyperthyroidism, and Bone Mass
Se-Min Kim, Vitaly Ryu, Sari Miyashita, et al.
Journal of Virology
|
June 16, 2006
Influenza virus evades innate and adaptive immunity via the NS1 protein
Ana Fernandez-Sesma, Svetlana Marukian, Barbara J Ebersole, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
May 8, 2019
Cytochrome c oxidase dysfunction enhances phagocytic function and osteoclast formation in macrophages
Rajesh Angireddy, Hasan Raza Kazmi, Satish Srinivasan, et al.
The Journal of Steroid Biochemistry and Molecular Biology
|
April 5, 2016
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia
Katja K Dumic, Zorana Grubic, Tony Yuen, et al.
Frontiers in Endocrinology
|
April 4, 2019
FSH Beyond Fertility
Daria Lizneva, Alina Rahimova, Se-Min Kim, et al.
Page
of 12