11 – 20 of 20
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- « previous
- 1
- 2
- next »
- 2011
-
Mark
Mitochondrial disorders caused by mutations in respiratory chain assembly factors
(
- 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
-
Mark
Mitochondrial hepatopathies in the newborn period.
(
- 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
- « previous
- 1
- 2
- next »