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The International Journal of Biochemistry & Cell Biology|April 15, 2014
Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse modelChadi Homedan, Jihane Laafi, Caroline Schmitt, et al.
Human Molecular Genetics|June 14, 2015
Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyriaChadi Homedan, Caroline Schmitt, Jihane Laafi, et al.
American Journal of Human Genetics|December 31, 2005
Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyriaLaurent Gouya, Caroline Martin-Schmitt, Anne-Marie Robreau, et al.
European Journal of Gastroenterology & Hepatology|July 12, 2008
The V249I polymorphism of the CX3CR1 gene is associated with fibrostenotic disease behavior in patients with Crohn's diseaseJean-Marc Sabate, Nejma Ameziane, Jérôme Lamoril, et al.
Human Molecular Genetics|September 15, 2005
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyriaCaroline Schmitt, Laurent Gouya, Eva Malonova, et al.
Blood|June 10, 2011
ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyriaJordi To-Figueras, Sarah Ducamp, Jerome Clayton, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 15, 2013
Epistasis in iron metabolism: complex interactions between Cp, Mon1a, and Slc40a1 loci and tissue iron in miceConstance Delaby, Vincent Oustric, Caroline Schmitt, et al.
European Radiology|October 25, 2021
Autofluorescence imaging within the liver: a promising tool for the detection and characterization of primary liver tumorsCharlotte Benoit, Aurélie Rodrigues, Julien Calderaro, et al.
Haematologica|February 2, 2017
Hemolytic anemia repressed hepcidin level without hepatocyte iron overload: lesson from Günther disease modelSarah Millot, Constance Delaby, Boualem Moulouel, et al.
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