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- 2021
-
Mark
Comparison of RNA- and DNA-based methods for measurable residual disease analysis in NPM1-mutated acute myeloid leukemia
2021) In International Journal of Laboratory Hematology(
- Contribution to journal › Article
- 2020
-
Mark
Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice
(
- Contribution to journal › Article
- 2017
-
Mark
A Turkish BCS1L mutation causes GRACILE-like disorder
(
- Contribution to journal › Article
- 2016
-
Mark
Effect of high-carbohydrate diet on plasma metabolome in mice with mitochondrial respiratory chain complex III deficiency
(
- Contribution to journal › Article
-
Mark
COX7A2L/SCAFI and pre-complex III modify respiratory chain supercomplex formation in different mouse strains with a Bcs1l mutation
(
- Contribution to journal › Article
- 2014
-
Mark
Complex I Function and Supercomplex Formation Are Preserved in Liver Mitochondria Despite Progressive Complex III Deficiency.
(
- Contribution to journal › Article
-
Mark
A mouse model of mitochondrial complex III dysfunction induced by myxothiazol.
(
- Contribution to journal › Article
- 2013
-
Mark
The radical-binding lipocalin A1M binds to a Complex I subunit and protects mitochondrial structure and function.
(
- Contribution to journal › Article
- 2012
-
Mark
Metabolite Profiles Reveal Energy Failure and Impaired Beta-Oxidation in Liver of Mice with Complex III Deficiency Due to a BCS1L Mutation.
(
- Contribution to journal › Article
- 2011
-
Mark
Complex III staining in blue native polyacrylamide gels
(
- Contribution to journal › Article
-
Mark
Mitochondrial disorders caused by mutations in respiratory chain assembly factors
(
- Contribution to journal › Article
-
Mark
Mitochondrial hepatopathies in the newborn period.
(
- Contribution to journal › Article
-
Mark
The GRACILE mutation introduced into Bcs1l causes postnatal complex III deficiency: A viable mouse model for mitochondrial hepatopathy.
(
- Contribution to journal › Article
- 2010
-
Mark
Bcs1L A232G mutant mice: A new model of complex III deficiency and hepatic cirrhosis
(
- Contribution to journal › Published meeting abstract
-
Mark
Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation.
(
- Contribution to journal › Article
-
Mark
A novel role for constitutively expressed epithelial-derived chemokines as antibacterial peptides in the intestinal mucosa.
(
- Contribution to journal › Article
- 2007
-
Mark
BCS1L is expressed in critical regions for neural development during ontogenesis in mice.
(
- Contribution to journal › Article
- 2003
-
Mark
Mechanisms of phagocytosis resistance in Streptococcus pyogenes
2003)(
- Thesis › Doctoral thesis (compilation)
- 2000
-
Mark
A role for the fibrinogen-binding regions of streptococcal M proteins in phagocytosis resistance
(
- Contribution to journal › Article
- 1998
-
Mark
Kringle 2 mediates high affinity binding of plasminogen to an internal sequence in streptococcal surface protein PAM.
(
- Contribution to journal › Article