Search research articles
Contact Us
Filters
Showing results (1-10 of 30) with videos related to
Page
of 3
Sort By:
Inflammatory Bowel Diseases
|
January 9, 2007
Litaf/Simple protein is increased in intestinal tissues from patients with CD and UC, but is unlikely to function as a transcription factor
Yongzhao Huang, Craig L Bennett
Journal of Genetic Syndromes & Gene Therapy
|
February 25, 2014
Microtubule defects & Neurodegeneration
Fiona J Baird, Craig L Bennett
Advances in Neurobiology
|
June 20, 2018
Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: From Normal Function to Pathological Roles in Motor Neuron Disease and Cerebellar Degeneration
Craig L Bennett, Albert R La Spada
Discovery Medicine
|
March 1, 2015
Unwinding the role of senataxin in neurodegeneration
Craig L Bennett, Albert R La Spada
Molecular Genetics & Genomic Medicine
|
July 15, 2021
SUMOylated Senataxin functions in genome stability, RNA degradation, and stress granule disassembly, and is linked with inherited ataxia and motor neuron disease
Craig L Bennett, Albert R La Spada
Heliyon
|
June 25, 2020
Tight expression regulation of senataxin, linked to motor neuron disease and ataxia, is required to avert cell-cycle block and nucleolus disassembly
Craig L Bennett, Bryce L Sopher, Albert R La Spada
American Journal of Medical Genetics
|
January 25, 2002
Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1
Ian P Blair, Roxanne R Gibson, Craig L Bennett, et al.
Journal of the Peripheral Nervous System : JPNS
|
December 3, 2003
New gene for CMT
Valerie A Street, Craig L Bennett, Thomas D Bird, et al.
Epilepsia
|
January 9, 2009
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients
Craig L Bennett, Yingzhang Chen, Sihoun Hahn, et al.
Journal of Neuroscience Research
|
August 25, 2005
SIMPLE interacts with NEDD4 and TSG101: evidence for a role in lysosomal sorting and implications for Charcot-Marie-Tooth disease
Andrew J Shirk, Susan K Anderson, Sayed H Hashemi, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Inflammatory Bowel Diseases
|
January 9, 2007
Litaf/Simple protein is increased in intestinal tissues from patients with CD and UC, but is unlikely to function as a transcription factor
Yongzhao Huang, Craig L Bennett
Journal of Genetic Syndromes & Gene Therapy
|
February 25, 2014
Microtubule defects & Neurodegeneration
Fiona J Baird, Craig L Bennett
Advances in Neurobiology
|
June 20, 2018
Senataxin, A Novel Helicase at the Interface of RNA Transcriptome Regulation and Neurobiology: From Normal Function to Pathological Roles in Motor Neuron Disease and Cerebellar Degeneration
Craig L Bennett, Albert R La Spada
Discovery Medicine
|
March 1, 2015
Unwinding the role of senataxin in neurodegeneration
Craig L Bennett, Albert R La Spada
Molecular Genetics & Genomic Medicine
|
July 15, 2021
SUMOylated Senataxin functions in genome stability, RNA degradation, and stress granule disassembly, and is linked with inherited ataxia and motor neuron disease
Craig L Bennett, Albert R La Spada
Heliyon
|
June 25, 2020
Tight expression regulation of senataxin, linked to motor neuron disease and ataxia, is required to avert cell-cycle block and nucleolus disassembly
Craig L Bennett, Bryce L Sopher, Albert R La Spada
American Journal of Medical Genetics
|
January 25, 2002
Search for genes involved in Joubert syndrome: evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1
Ian P Blair, Roxanne R Gibson, Craig L Bennett, et al.
Journal of the Peripheral Nervous System : JPNS
|
December 3, 2003
New gene for CMT
Valerie A Street, Craig L Bennett, Thomas D Bird, et al.
Epilepsia
|
January 9, 2009
Prevalence of ALDH7A1 mutations in 18 North American pyridoxine-dependent seizure (PDS) patients
Craig L Bennett, Yingzhang Chen, Sihoun Hahn, et al.
Journal of Neuroscience Research
|
August 25, 2005
SIMPLE interacts with NEDD4 and TSG101: evidence for a role in lysosomal sorting and implications for Charcot-Marie-Tooth disease
Andrew J Shirk, Susan K Anderson, Sayed H Hashemi, et al.
Page
of 3