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Journal of Hepatology
|
December 2, 1998
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
M Sánchez, M Bruguera, J Bosch, et al.
Molecular Reproduction and Development
|
June 11, 1998
Protein and DNA contents in sperm from an infertile human male possessing protamine defects that vary over time
G Bench, M H Corzett, L De Yebra, et al.
Neuroscience Letters
|
April 21, 1995
Apolipoprotein E4 allele frequency in Spanish Alzheimer and control cases
R Adroer, P Santacruz, R Blesa, et al.
American Journal of Medical Genetics
|
December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite
E Margarit, M D Coll, R Oliva, et al.
Oncotarget
|
April 30, 2017
Repositioning chlorpromazine for treating chemoresistant glioma through the inhibition of cytochrome c oxidase bearing the COX4-1 regulatory subunit
Claudia R Oliva, Wei Zhang, Cathy Langford, et al.
Diabetes, Obesity & Metabolism
|
September 30, 2011
Effects of combining simvastatin with rosiglitazone on inflammation, oxidant stress and ambulatory blood pressure in patients with the metabolic syndrome: the SIROCO study
I Lazich, P Sarafidis, E de Guzman, et al.
Neurology
|
February 20, 1999
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
M Ezquerra, C Carnero, R Blesa, et al.
The Journal of Biological Chemistry
|
May 15, 1993
Complete selective absence of protamine P2 in humans
L de Yebra, J L Ballescà, J A Vanrell, et al.
Experimental Brain Research
|
September 26, 2003
Expression of c-fos in auditory and non-auditory brain regions of the gerbil after manipulations that induce tinnitus
E Wallhäusser-Franke, C Mahlke, R Oliva, et al.
Medicina Clinica
|
June 20, 2001
[Sporadic and familial Parkinson's disease: comparative study]
E Muñoz, P Pastor, M José Martí, et al.
Page
of 21
Search research articles
Search
Showing results (71-80 of 203) with videos related to
Sort By:
Page
of 21
Journal of Hepatology
|
December 2, 1998
Prevalence of the Cys282Tyr and His63Asp HFE gene mutations in Spanish patients with hereditary hemochromatosis and in controls
M Sánchez, M Bruguera, J Bosch, et al.
Molecular Reproduction and Development
|
June 11, 1998
Protein and DNA contents in sperm from an infertile human male possessing protamine defects that vary over time
G Bench, M H Corzett, L De Yebra, et al.
Neuroscience Letters
|
April 21, 1995
Apolipoprotein E4 allele frequency in Spanish Alzheimer and control cases
R Adroer, P Santacruz, R Blesa, et al.
American Journal of Medical Genetics
|
December 22, 1999
SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite
E Margarit, M D Coll, R Oliva, et al.
Oncotarget
|
April 30, 2017
Repositioning chlorpromazine for treating chemoresistant glioma through the inhibition of cytochrome c oxidase bearing the COX4-1 regulatory subunit
Claudia R Oliva, Wei Zhang, Cathy Langford, et al.
Diabetes, Obesity & Metabolism
|
September 30, 2011
Effects of combining simvastatin with rosiglitazone on inflammation, oxidant stress and ambulatory blood pressure in patients with the metabolic syndrome: the SIROCO study
I Lazich, P Sarafidis, E de Guzman, et al.
Neurology
|
February 20, 1999
A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures
M Ezquerra, C Carnero, R Blesa, et al.
The Journal of Biological Chemistry
|
May 15, 1993
Complete selective absence of protamine P2 in humans
L de Yebra, J L Ballescà, J A Vanrell, et al.
Experimental Brain Research
|
September 26, 2003
Expression of c-fos in auditory and non-auditory brain regions of the gerbil after manipulations that induce tinnitus
E Wallhäusser-Franke, C Mahlke, R Oliva, et al.
Medicina Clinica
|
June 20, 2001
[Sporadic and familial Parkinson's disease: comparative study]
E Muñoz, P Pastor, M José Martí, et al.
Page
of 21