Genetic strategies for dissecting mammalian and Drosophila voltage-dependent anion channel functions

Por Craigen, William J., Graham, Brett H.
Publicado no J Bioenerg Biomembr (2008)

Nek1 regulates cell death and mitochondrial membrane permeability through phosphorylation of VDAC1

Por Chen, Yumay, Craigen, William J., Riley, Daniel J.
Publicado em 2009

Isoform-Specific Imprinting of the Human PEG1/MEST Gene

Por Kosaki, Kenjiro, Kosaki, Rika, Craigen, William J., Matsuo, Nobutake
Publicado em 2000

New Insights into the Mechanism of Permeation through Large Channels

Por Komarov, Alexander G., Deng, Defeng, Craigen, William J., Colombini, Marco
Publicado em 2005

Reduced VDAC1 Protects Against Alzheimer’s Disease, Mitochondria and Synaptic Deficiencies

Por Manczak, Maria, Sheiko, Tatiana, Craigen, William J., Reddy, P. Hemachandra
Publicado em 2013

Voltage-dependant anion channels: Novel insights into isoform function through genetic models()

Por Raghavan, Adithya, Sheiko, Tatiana, Graham, Brett H., Craigen, William J.
Publicado no Biochim Biophys Acta (2011)

The Physiological Properties of a Novel Family of VDAC-Like Proteins from Drosophila melanogaster

Por Komarov, Alexander G., Graham, Brett H., Craigen, William J., Colombini, Marco
Publicado em 2004

VDAC2 is required for truncated BID-induced mitochondrial apoptosis by recruiting BAK to the mitochondria

Por Roy, Soumya Sinha, Ehrlich, Amy M, Craigen, William J, Hajnóczky, György
Publicado em 2009

VDAC3 has differing mitochondrial functions in two types of striated muscles

Por Anflous-Pharayra, Keltoum, Lee, Nha, Armstrong, Dawna L., Craigen, William J.
Publicado em 2010

Arrhythmia as a cardiac manifestation in MELAS syndrome()

Por Thomas, Tamara, Craigen, William J., Moore, Ryan, Czosek, Richard, Jefferies, John L.
Publicado no Mol Genet Metab Rep (2015)

Voltage-Dependent Anion Channels are Dispensable for Mitochondrial-Dependent Cell Death

Por Baines, Christopher P., Kaiser, Robert A., Sheiko, Tatiana, Craigen, William J., Molkentin, Jeffery D.
Publicado em 2007

The effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndrome()

Por El-Hattab, Ayman W., Emrick, Lisa T., Williamson, Kaitlin C., Craigen, William J., Scaglia, Fernando
Publicado em 2013

Expanding the phenotypic spectrum of Succinyl-CoA Ligase Deficiency through functional validation of a new SUCLG1 variant

Por Donti, Taraka R., Masand, Ruchi, Scott, Daryl A., Craigen, William J., Graham, Brett H
Publicado no Mol Genet Metab (2016)

Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletion

Por Donti, Taraka R., Stromberger, Carmen, Ge, Ming, Eldin, Karen W., Craigen, William J., Graham, Brett H.
Publicado em 2014

Neurologic Dysfunction and Male Infertility in Drosophila porin Mutants: A NEW MODEL FOR MITOCHONDRIAL DYSFUNCTION AND DISEASE

Por Graham, Brett H., Li, Zhihong, Alesii, Erminio P., Versteken, Patrik, Lee, Cynthia, Wang, Jennifer, Craigen, William J.
Publicado em 2010

Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology

Por Craigen, William J, Graham, Brett H, Wong, Lee-Jun, Scaglia, Fernando, Lewis, Richard Alan, Bonnen, Penelope E
Publicado em 2013

Novel cardiovascular findings in association with a POMT2 mutation: three siblings with α-dystroglycanopathy

Por Martinez, Hugo R, Craigen, William J, Ummat, Monika, Adesina, Adekunle M, Lotze, Timothy E, Jefferies, John L
Publicado em 2014

Mitochondrial Dysfunction Mediated by Poly(ADP-Ribose) Polymerase-1 Activation Contributes to Hippocampal Neuronal Damage Following Status Epilepticus

Por Lai, Yi-Chen, Baker, J. Scott, Donti, Taraka, Graham, Brett H., Craigen, William J., Anderson, Anne E.
Publicado no Int J Mol Sci (2017)

Generation of a novel mouse model that recapitulates early and adult onset glycogenosis type IV

Por Akman, H. Orhan, Sheiko, Tatiana, Tay, Stacey K.H., Finegold, Milton J., DiMauro, Salvatore, Craigen, William J.
Publicado em 2011

Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation

Por El-Hattab, Ayman W., Emrick, Lisa T., Hsu, Jean W., Chanprasert, Sirisak, Jahoor, Farook, Scaglia, Fernando, Craigen, William J.
Publicado no Mitochondrion (2014)