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Apoptosis : an International Journal on Programmed Cell Death
|
November 25, 2003
Signalling steps in apoptosis by ether lipids
L A Smets, H Van Rooij, G S Salomons
Neuropediatrics
|
July 13, 2004
D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?
S H Korman, G S Salomons, A Gutman, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[L-2-hydroxyglutaric aciduria: report on two cases]
S Wagner, C Vianey-Saban, G-S Salomons, et al.
The EMBO Journal
|
March 15, 1996
T cells from baxalpha transgenic mice show accelerated apoptosis in response to stimuli but do not show restored DNA damage-induced cell death in the absence of p53
H J Brady, G S Salomons, R C Bobeldijk, et al.
Journal of Inherited Metabolic Disease
|
March 14, 2009
Measurement of D: -2-hydroxyglutarate dehydrogenase activity in cell homogenates derived from D: -2-hydroxyglutaric aciduria patients
W V Wickenhagen, G S Salomons, K M Gibson, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 12, 2004
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency
A Dervent, K M Gibson, P L Pearl, et al.
Biochimica Et Biophysica Acta
|
September 6, 2011
A lymphoblast model for IDH2 gain-of-function activity in d-2-hydroxyglutaric aciduria type II: novel avenues for biochemical and therapeutic studies
M Kranendijk, G S Salomons, K M Gibson, et al.
Molecular Genetics and Metabolism
|
April 3, 2004
The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family
S Bekri, C Fossoud, G Plaza, et al.
Molecular Genetics and Metabolism
|
June 1, 2007
Mutation analysis a prerequisite for prenatal diagnosis of L-2-hydroxyglutaric aciduria?
P Augoustides-Savvopoulou, G S Salomons, J Dotis, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 6, 2016
Therapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism
K R Vogel, G R Ainslie, E E W Jansen, et al.
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of 6
Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Apoptosis : an International Journal on Programmed Cell Death
|
November 25, 2003
Signalling steps in apoptosis by ether lipids
L A Smets, H Van Rooij, G S Salomons
Neuropediatrics
|
July 13, 2004
D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?
S H Korman, G S Salomons, A Gutman, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 11, 2013
[L-2-hydroxyglutaric aciduria: report on two cases]
S Wagner, C Vianey-Saban, G-S Salomons, et al.
The EMBO Journal
|
March 15, 1996
T cells from baxalpha transgenic mice show accelerated apoptosis in response to stimuli but do not show restored DNA damage-induced cell death in the absence of p53
H J Brady, G S Salomons, R C Bobeldijk, et al.
Journal of Inherited Metabolic Disease
|
March 14, 2009
Measurement of D: -2-hydroxyglutarate dehydrogenase activity in cell homogenates derived from D: -2-hydroxyglutaric aciduria patients
W V Wickenhagen, G S Salomons, K M Gibson, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 12, 2004
Photosensitive absence epilepsy with myoclonias and heterozygosity for succinic semialdehyde dehydrogenase (SSADH) deficiency
A Dervent, K M Gibson, P L Pearl, et al.
Biochimica Et Biophysica Acta
|
September 6, 2011
A lymphoblast model for IDH2 gain-of-function activity in d-2-hydroxyglutaric aciduria type II: novel avenues for biochemical and therapeutic studies
M Kranendijk, G S Salomons, K M Gibson, et al.
Molecular Genetics and Metabolism
|
April 3, 2004
The molecular basis of succinic semialdehyde dehydrogenase deficiency in one family
S Bekri, C Fossoud, G Plaza, et al.
Molecular Genetics and Metabolism
|
June 1, 2007
Mutation analysis a prerequisite for prenatal diagnosis of L-2-hydroxyglutaric aciduria?
P Augoustides-Savvopoulou, G S Salomons, J Dotis, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
November 6, 2016
Therapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism
K R Vogel, G R Ainslie, E E W Jansen, et al.
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of 6