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Journal of Medicinal Chemistry
|
February 11, 2010
Biological and biophysical properties of the histone deacetylase inhibitor suberoylanilide hydroxamic acid are affected by the presence of short alkyl groups on the phenyl ring
Frédérik Oger, Aurélien Lecorgne, Elisa Sala, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 3, 2024
A Systematic Review Supporting the Endocrine Society Clinical Practice Guidelines on Vitamin D
Vishal Paresh Shah, Tarek Nayfeh, Yahya Alsawaf, et al.
The Journal of Surgical Research
|
November 23, 2018
Loss of Intestinal Alkaline Phosphatase Leads to Distinct Chronic Changes in Bone Phenotype
Florian Kuehn, Fatemeh Adiliaghdam, Sulaiman R Hamarneh, et al.
Revue Neurologique
|
January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]
R Ben Yaou, H-M Bécane, L Demay, et al.
Journal of Neurology
|
October 17, 2018
Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series
Eun-Joo Kim, Jesse A Brown, Jersey Deng, et al.
Leukemia
|
October 1, 2016
Copy-number analysis identified new prognostic marker in acute myeloid leukemia
O Nibourel, S Guihard, C Roumier, et al.
Science Translational Medicine
|
November 25, 2016
Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification
Devaveena Dey, Jana Bagarova, Sarah J Hatsell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 3, 2024
Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline
Marie B Demay, Anastassios G Pittas, Daniel D Bikle, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 17, 2007
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations
Irène Netchine, Sylvie Rossignol, Marie-Noëlle Dufourg, et al.
Elife
|
April 3, 2024
Vitamin D constrains inflammation by modulating the expression of key genes on Chr17q12-21.1
Ayse Kilic, Arda Halu, Margherita De Marzio, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 288) with videos related to
Sort By:
Page
of 29
Journal of Medicinal Chemistry
|
February 11, 2010
Biological and biophysical properties of the histone deacetylase inhibitor suberoylanilide hydroxamic acid are affected by the presence of short alkyl groups on the phenyl ring
Frédérik Oger, Aurélien Lecorgne, Elisa Sala, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 3, 2024
A Systematic Review Supporting the Endocrine Society Clinical Practice Guidelines on Vitamin D
Vishal Paresh Shah, Tarek Nayfeh, Yahya Alsawaf, et al.
The Journal of Surgical Research
|
November 23, 2018
Loss of Intestinal Alkaline Phosphatase Leads to Distinct Chronic Changes in Bone Phenotype
Florian Kuehn, Fatemeh Adiliaghdam, Sulaiman R Hamarneh, et al.
Revue Neurologique
|
January 29, 2005
[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations]
R Ben Yaou, H-M Bécane, L Demay, et al.
Journal of Neurology
|
October 17, 2018
Mixed TDP-43 proteinopathy and tauopathy in frontotemporal lobar degeneration: nine case series
Eun-Joo Kim, Jesse A Brown, Jersey Deng, et al.
Leukemia
|
October 1, 2016
Copy-number analysis identified new prognostic marker in acute myeloid leukemia
O Nibourel, S Guihard, C Roumier, et al.
Science Translational Medicine
|
November 25, 2016
Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification
Devaveena Dey, Jana Bagarova, Sarah J Hatsell, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 3, 2024
Vitamin D for the Prevention of Disease: An Endocrine Society Clinical Practice Guideline
Marie B Demay, Anastassios G Pittas, Daniel D Bikle, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 17, 2007
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations
Irène Netchine, Sylvie Rossignol, Marie-Noëlle Dufourg, et al.
Elife
|
April 3, 2024
Vitamin D constrains inflammation by modulating the expression of key genes on Chr17q12-21.1
Ayse Kilic, Arda Halu, Margherita De Marzio, et al.
Page
of 29