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The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2009
A molecular basis for variation in clinical severity of isolated growth hormone deficiency type II
Rizwan Hamid, John A Phillips, Cindy Holladay, et al.
American Journal of Respiratory Cell and Molecular Biology
|
January 1, 2021
TBX4 Transcription Factor Is a Positive Feedback Regulator of Itself and Phospho-SMAD1/5
Ying Cai, Ling Yan, Matthew J Kielt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2000
Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene
F Pernasetti, S P Toledo, V V Vasilyev, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study
J D Cogan, B Ramel, M Lehto, et al.
BMJ Open Sport & Exercise Medicine
|
October 10, 2025
Update on sport mental health assessment tool-1 false negative rates from the 2024 Paris Olympic and Paralympic Games
Travis Anderson, Jessica Bartley, Angel Brutus, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2018
Phenotypic heterogeneity of ZMPSTE24 deficiency
Thomas A Cassini, Amy K Robertson, Anna G Bican, et al.
Irish Medical Journal
|
March 13, 2022
Achalasia in a Young Woman Thought to Have Had an Eating Disorder
C McAteer, M Imran, K Van Der Merwe, et al.
American Journal of Medical Genetics. Part A
|
August 25, 2023
A medical odyssey of a 72-year-old man with Charcot-Marie-Tooth disease type 2 newly diagnosed with biallelic variants in SORD gene causing sorbitol dehydrogenase deficiency
Yutaka Furuta, Erica T Nelson, Serena M Neumann, et al.
Pulmonary Circulation
|
February 21, 2025
RNA-Seq and ChIP-Seq Identification of Unique and Overlapping Target Genes and Pathways Regulated by TBX4 in Human Pulmonary Fibroblasts and Pericytes
Ying Cai, Ling Yan, Joy D Cogan, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
August 12, 1998
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions
I J Arnhold, M G Osorio, S B Oliveira, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 103) with videos related to
Sort By:
Page
of 11
The Journal of Clinical Endocrinology and Metabolism
|
October 20, 2009
A molecular basis for variation in clinical severity of isolated growth hormone deficiency type II
Rizwan Hamid, John A Phillips, Cindy Holladay, et al.
American Journal of Respiratory Cell and Molecular Biology
|
January 1, 2021
TBX4 Transcription Factor Is a Positive Feedback Regulator of Itself and Phospho-SMAD1/5
Ying Cai, Ling Yan, Matthew J Kielt, et al.
The Journal of Clinical Endocrinology and Metabolism
|
January 14, 2000
Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene
F Pernasetti, S P Toledo, V V Vasilyev, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 1, 1995
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study
J D Cogan, B Ramel, M Lehto, et al.
BMJ Open Sport & Exercise Medicine
|
October 10, 2025
Update on sport mental health assessment tool-1 false negative rates from the 2024 Paris Olympic and Paralympic Games
Travis Anderson, Jessica Bartley, Angel Brutus, et al.
American Journal of Medical Genetics. Part A
|
January 18, 2018
Phenotypic heterogeneity of ZMPSTE24 deficiency
Thomas A Cassini, Amy K Robertson, Anna G Bican, et al.
Irish Medical Journal
|
March 13, 2022
Achalasia in a Young Woman Thought to Have Had an Eating Disorder
C McAteer, M Imran, K Van Der Merwe, et al.
American Journal of Medical Genetics. Part A
|
August 25, 2023
A medical odyssey of a 72-year-old man with Charcot-Marie-Tooth disease type 2 newly diagnosed with biallelic variants in SORD gene causing sorbitol dehydrogenase deficiency
Yutaka Furuta, Erica T Nelson, Serena M Neumann, et al.
Pulmonary Circulation
|
February 21, 2025
RNA-Seq and ChIP-Seq Identification of Unique and Overlapping Target Genes and Pathways Regulated by TBX4 in Human Pulmonary Fibroblasts and Pericytes
Ying Cai, Ling Yan, Joy D Cogan, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
August 12, 1998
Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions
I J Arnhold, M G Osorio, S B Oliveira, et al.
Page
of 11