Search research articles
Contact Us
Filters
Showing results (1111-1120 of 1,983) with videos related to
Page
of 199
Sort By:
FEBS Letters
|
December 14, 2001
Depolarisation induces rapid and transient formation of intracellular sphingosine-1-phosphate
R Alemany, B Kleuser, L Ruwisch, et al.
European Journal of Pediatrics
|
March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome
E Lopriore, R J Gemke, N M Verhoeven, et al.
Journal of Child Neurology
|
March 1, 1995
D-2-hydroxyglutaric aciduria
W L Nyhan, G D Shelton, C Jakobs, et al.
Neural Regeneration Research
|
February 5, 2026
Mesenchymal stem cell-derived extracellular vesicle treatment of induced pluripotent stem cell-derived motor neurons with different amyotrophic lateral sclerosis genetic backgrounds
Suzy Varderidou-Minasian, Channa E Jakobs, Svetlana Pasteuning-Vuhman, et al.
Journal of Structural Biology
|
December 1, 2025
Dual-colour super-resolution cryoCLEM in mammalian cells using the fluorescent proteins rsTagRFP and rsEGFP2
Mart G F Last, Maartje van Klaveren, Lennert Janssen, et al.
Nature Genetics
|
November 1, 1995
Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p
M Whitney, M Thayer, C Reifsteck, et al.
Environmental Health : a Global Access Science Source
|
June 20, 2015
Long-term exposure to fine particulate matter and incidence of type 2 diabetes mellitus in a cohort study: effects of total and traffic-specific air pollution
Gudrun Weinmayr, Frauke Hennig, Kateryna Fuks, et al.
British Journal of Haematology
|
February 1, 2006
Cellular folate vitamer distribution during and after correction of vitamin B12 deficiency: a case for the methylfolate trap
Y M Smulders, D E C Smith, R M Kok, et al.
American Journal of Human Genetics
|
December 21, 2004
Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria
Eduard A Struys, Gajja S Salomons, Younes Achouri, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect
R J Wanders, C W van Roermund, W Lageweg, et al.
Page
of 199
Search research articles
Search
Showing results (1111-1120 of 1,983) with videos related to
Sort By:
Page
of 199
FEBS Letters
|
December 14, 2001
Depolarisation induces rapid and transient formation of intracellular sphingosine-1-phosphate
R Alemany, B Kleuser, L Ruwisch, et al.
European Journal of Pediatrics
|
March 29, 2001
Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome
E Lopriore, R J Gemke, N M Verhoeven, et al.
Journal of Child Neurology
|
March 1, 1995
D-2-hydroxyglutaric aciduria
W L Nyhan, G D Shelton, C Jakobs, et al.
Neural Regeneration Research
|
February 5, 2026
Mesenchymal stem cell-derived extracellular vesicle treatment of induced pluripotent stem cell-derived motor neurons with different amyotrophic lateral sclerosis genetic backgrounds
Suzy Varderidou-Minasian, Channa E Jakobs, Svetlana Pasteuning-Vuhman, et al.
Journal of Structural Biology
|
December 1, 2025
Dual-colour super-resolution cryoCLEM in mammalian cells using the fluorescent proteins rsTagRFP and rsEGFP2
Mart G F Last, Maartje van Klaveren, Lennert Janssen, et al.
Nature Genetics
|
November 1, 1995
Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p
M Whitney, M Thayer, C Reifsteck, et al.
Environmental Health : a Global Access Science Source
|
June 20, 2015
Long-term exposure to fine particulate matter and incidence of type 2 diabetes mellitus in a cohort study: effects of total and traffic-specific air pollution
Gudrun Weinmayr, Frauke Hennig, Kateryna Fuks, et al.
British Journal of Haematology
|
February 1, 2006
Cellular folate vitamer distribution during and after correction of vitamin B12 deficiency: a case for the methylfolate trap
Y M Smulders, D E C Smith, R M Kok, et al.
American Journal of Human Genetics
|
December 21, 2004
Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria
Eduard A Struys, Gajja S Salomons, Younes Achouri, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
X-linked adrenoleukodystrophy: biochemical diagnosis and enzyme defect
R J Wanders, C W van Roermund, W Lageweg, et al.
Page
of 199