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Journal of Photochemistry and Photobiology. B, Biology
|
April 15, 1990
Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing mice
A M Richter, S Cerruti-Sola, E D Sternberg, et al.
Cytokines and Molecular Therapy
|
March 1, 1996
Control of stroma-dependent hematopoiesis by basic fibroblast growth factor: stromal phenotypic plasticity and modified myelopoietic functions
D Sternberg, A Peled, E Shezen, et al.
Pediatric Research
|
August 6, 2000
Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes)
A Bakker, C Barthélémy, P Frachon, et al.
Revue Neurologique
|
December 12, 2018
Abundant electrical myotonia and left ventricular noncompaction: Unusual features of Danon disease due to a novel mutation in LAMP2 gene
P Codron, V Pautot, A Tassin, et al.
Journal of Lipid Research
|
November 28, 1997
Analysis of a Chinese hamster ovary cell mutant with defective mobilization of cholesterol from the plasma membrane to the endoplasmic reticulum
N L Jacobs, B Andemariam, K W Underwood, et al.
Photochemistry and Photobiology
|
September 1, 1990
In vitro evaluation of phototoxic properties of four structurally related benzoporphyrin derivatives
A M Richter, E Waterfield, A K Jain, et al.
Journal of Health Communication
|
February 16, 2018
Integrating Models of Diffusion and Behavior to Predict Innovation Adoption, Maintenance, and Social Diffusion
Rachel A Smith, Youllee Kim, Xun Zhu, et al.
Revue Neurologique
|
January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]
P Laforêt, F Ziegler, D Sternberg, et al.
Journal of Neurology
|
October 31, 2012
Pregnancy in congenital myasthenic syndrome
L Servais, H Baudoin, K Zehrouni, et al.
Revue Neurologique
|
February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families
M I Kediha, M Tazir, C Magnouche, et al.
Page
of 10
Search research articles
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Showing results (41-50 of 94) with videos related to
Sort By:
Page
of 10
Journal of Photochemistry and Photobiology. B, Biology
|
April 15, 1990
Biodistribution of tritiated benzoporphyrin derivative (3H-BPD-MA), a new potent photosensitizer, in normal and tumor-bearing mice
A M Richter, S Cerruti-Sola, E D Sternberg, et al.
Cytokines and Molecular Therapy
|
March 1, 1996
Control of stroma-dependent hematopoiesis by basic fibroblast growth factor: stromal phenotypic plasticity and modified myelopoietic functions
D Sternberg, A Peled, E Shezen, et al.
Pediatric Research
|
August 6, 2000
Functional mitochondrial heterogeneity in heteroplasmic cells carrying the mitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes)
A Bakker, C Barthélémy, P Frachon, et al.
Revue Neurologique
|
December 12, 2018
Abundant electrical myotonia and left ventricular noncompaction: Unusual features of Danon disease due to a novel mutation in LAMP2 gene
P Codron, V Pautot, A Tassin, et al.
Journal of Lipid Research
|
November 28, 1997
Analysis of a Chinese hamster ovary cell mutant with defective mobilization of cholesterol from the plasma membrane to the endoplasmic reticulum
N L Jacobs, B Andemariam, K W Underwood, et al.
Photochemistry and Photobiology
|
September 1, 1990
In vitro evaluation of phototoxic properties of four structurally related benzoporphyrin derivatives
A M Richter, E Waterfield, A K Jain, et al.
Journal of Health Communication
|
February 16, 2018
Integrating Models of Diffusion and Behavior to Predict Innovation Adoption, Maintenance, and Social Diffusion
Rachel A Smith, Youllee Kim, Xun Zhu, et al.
Revue Neurologique
|
January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]
P Laforêt, F Ziegler, D Sternberg, et al.
Journal of Neurology
|
October 31, 2012
Pregnancy in congenital myasthenic syndrome
L Servais, H Baudoin, K Zehrouni, et al.
Revue Neurologique
|
February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families
M I Kediha, M Tazir, C Magnouche, et al.
Page
of 10