Search research articles
Contact Us
Filters
Showing results (51-60 of 55) with videos related to
Page
of 6
Sort By:
You have reached the last page of results.
This site can display upto 55 results.
Molecular Vision
|
December 15, 2006
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Veronique Vieira, Gabriel David, Olivier Roche, et al.
Diabetes
|
November 25, 2005
Resistance to diet-induced obesity in mu-opioid receptor-deficient mice: evidence for a "thrifty gene"
Antoine Tabarin, Y Diz-Chaves, Yolanda Diz Chaves, et al.
The Journal of Biological Chemistry
|
September 11, 2002
High level of uncoupling protein 1 expression in muscle of transgenic mice selectively affects muscles at rest and decreases their IIb fiber content
Elodie Couplan, Chantal Gelly, Marc Goubern, et al.
Molecular Vision
|
April 10, 2007
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities
Anouk Dansault, Gabriel David, Claire Schwartz, et al.
Human Mutation
|
May 12, 2011
Clinical and biochemical heterogeneity associated with fumarase deficiency
Chris Ottolenghi, Laurence Hubert, Yannick Allanore, et al.
Page
of 6
Search research articles
Search
Showing results (51-60 of 55) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 55 results.
Molecular Vision
|
December 15, 2006
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
Veronique Vieira, Gabriel David, Olivier Roche, et al.
Diabetes
|
November 25, 2005
Resistance to diet-induced obesity in mu-opioid receptor-deficient mice: evidence for a "thrifty gene"
Antoine Tabarin, Y Diz-Chaves, Yolanda Diz Chaves, et al.
The Journal of Biological Chemistry
|
September 11, 2002
High level of uncoupling protein 1 expression in muscle of transgenic mice selectively affects muscles at rest and decreases their IIb fiber content
Elodie Couplan, Chantal Gelly, Marc Goubern, et al.
Molecular Vision
|
April 10, 2007
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities
Anouk Dansault, Gabriel David, Claire Schwartz, et al.
Human Mutation
|
May 12, 2011
Clinical and biochemical heterogeneity associated with fumarase deficiency
Chris Ottolenghi, Laurence Hubert, Yannick Allanore, et al.
Page
of 6