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Dilek Colak

Showing results (121-130 of 145) with videos related to

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Dose-Response : a Publication of International Hormesis Society|June 28, 2021
Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in OncogenesisMohammed S Aldughaim, Mashael R Al-Anazi, Marie Fe F Bohol, et al.
American Journal of Human Genetics|March 29, 2016
Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and MiceRanad Shaheen, Shams Anazi, Tawfeg Ben-Omran, et al.
Genomics|October 12, 2010
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathwaysDilek Colak, Hesham Al-Dhalaan, Michael Nester, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIIINamik Kaya, Hesham Aldhalaan, Banan Al-Younes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2008
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan diseaseNamik Kaya, Faiqa Imtiaz, Dilek Colak, et al.
American Journal of Human Genetics|October 1, 2013
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delayMoeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, et al.
The Journal of Biological Chemistry|May 8, 2022
Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndromeGhada I Aboheimed, Maha M AlRasheed, Sultan Almudimeegh, et al.
JIMD Reports|July 14, 2021
SLC25A42-associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletionMazhor Aldosary, Shahad Baselm, Maha Abdulrahim, et al.
Journal of Inherited Metabolic Disease|September 20, 2012
Clinical and biochemical features associated with BCS1L mutationMohammed Al-Owain, Dilek Colak, Albandary Albakheet, et al.
Cell Stem Cell|April 9, 2013
Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected]Swetlana Sirko, Gwendolyn Behrendt, Pia Annette Johansson, et al.
Pageof 15

Showing results (121-130 of 145) with videos related to

Sort By:
Pageof 15
Dose-Response : a Publication of International Hormesis Society|June 28, 2021
Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in OncogenesisMohammed S Aldughaim, Mashael R Al-Anazi, Marie Fe F Bohol, et al.
American Journal of Human Genetics|March 29, 2016
Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and MiceRanad Shaheen, Shams Anazi, Tawfeg Ben-Omran, et al.
Genomics|October 12, 2010
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathwaysDilek Colak, Hesham Al-Dhalaan, Michael Nester, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIIINamik Kaya, Hesham Aldhalaan, Banan Al-Younes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2008
Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan diseaseNamik Kaya, Faiqa Imtiaz, Dilek Colak, et al.
American Journal of Human Genetics|October 1, 2013
Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delayMoeenaldeen D Al-Sayed, Hamad Al-Zaidan, Albandary Albakheet, et al.
The Journal of Biological Chemistry|May 8, 2022
Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndromeGhada I Aboheimed, Maha M AlRasheed, Sultan Almudimeegh, et al.
JIMD Reports|July 14, 2021
SLC25A42-associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletionMazhor Aldosary, Shahad Baselm, Maha Abdulrahim, et al.
Journal of Inherited Metabolic Disease|September 20, 2012
Clinical and biochemical features associated with BCS1L mutationMohammed Al-Owain, Dilek Colak, Albandary Albakheet, et al.
Cell Stem Cell|April 9, 2013
Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected]Swetlana Sirko, Gwendolyn Behrendt, Pia Annette Johansson, et al.
Pageof 15