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The Journal of Investigative Dermatology
|
September 18, 1998
Induction of interleukin-6 production by ultraviolet radiation in normal human epidermal keratinocytes and in a human keratinocyte cell line is mediated by DNA damage
C Petit-Frère, P H Clingen, M Grewe, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
November 1, 2006
Emergence of Clostridium difficile toxinotype III, PCR-ribotype 027-associated disease, France, 2006
B Coignard, F Barbut, K Blanckaert, et al.
Scientific Reports
|
June 28, 2017
Magnetic particles with perpendicular anisotropy for mechanical cancer cell destruction
Rhodri Mansell, Tarun Vemulkar, Dorothée C M C Petit, et al.
European Journal of Pharmacology
|
August 6, 1991
Brain kinetics and specific binding of [11C]PK 11195 to omega 3 sites in baboons: positron emission tomography study
M C Petit-Taboué, J C Baron, L Barré, et al.
The British Journal of Dermatology
|
July 17, 2001
Contrasting effects of an ultraviolet B and an ultraviolet A tanning lamp on interleukin-6, tumour necrosis factor-alpha and intercellular adhesion molecule-1 expression
P H Clingen, M Berneburg, C Petit-Frère, et al.
FEBS Letters
|
December 31, 2002
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness
R Bruzzone, V Veronesi, D Gomès, et al.
Journal of Clinical Microbiology
|
July 6, 2000
Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile
P Bidet, V Lalande, B Salauze, et al.
Neuropsychologia
|
July 1, 1995
Healthy aging, memory subsystems and regional cerebral oxygen consumption
F Eustache, P Rioux, B Desgranges, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndrome
J P Hardelin, J Levilliers, J Young, et al.
Human Molecular Genetics
|
July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22
H Chaib, C Place, N Salem, et al.
Page
of 57
Search research articles
Search
Showing results (411-420 of 563) with videos related to
Sort By:
Page
of 57
The Journal of Investigative Dermatology
|
September 18, 1998
Induction of interleukin-6 production by ultraviolet radiation in normal human epidermal keratinocytes and in a human keratinocyte cell line is mediated by DNA damage
C Petit-Frère, P H Clingen, M Grewe, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin
|
November 1, 2006
Emergence of Clostridium difficile toxinotype III, PCR-ribotype 027-associated disease, France, 2006
B Coignard, F Barbut, K Blanckaert, et al.
Scientific Reports
|
June 28, 2017
Magnetic particles with perpendicular anisotropy for mechanical cancer cell destruction
Rhodri Mansell, Tarun Vemulkar, Dorothée C M C Petit, et al.
European Journal of Pharmacology
|
August 6, 1991
Brain kinetics and specific binding of [11C]PK 11195 to omega 3 sites in baboons: positron emission tomography study
M C Petit-Taboué, J C Baron, L Barré, et al.
The British Journal of Dermatology
|
July 17, 2001
Contrasting effects of an ultraviolet B and an ultraviolet A tanning lamp on interleukin-6, tumour necrosis factor-alpha and intercellular adhesion molecule-1 expression
P H Clingen, M Berneburg, C Petit-Frère, et al.
FEBS Letters
|
December 31, 2002
Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness
R Bruzzone, V Veronesi, D Gomès, et al.
Journal of Clinical Microbiology
|
July 6, 2000
Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile
P Bidet, V Lalande, B Salauze, et al.
Neuropsychologia
|
July 1, 1995
Healthy aging, memory subsystems and regional cerebral oxygen consumption
F Eustache, P Rioux, B Desgranges, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1993
Xp22.3 deletions in isolated familial Kallmann's syndrome
J P Hardelin, J Levilliers, J Young, et al.
Human Molecular Genetics
|
July 1, 1996
Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22
H Chaib, C Place, N Salem, et al.
Page
of 57