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Dilek Colak

Showing results (111-120 of 145) with videos related to

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Genes|January 21, 2022
A Novel <i>GEMIN4</i> Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and CataractsHesham Aldhalaan, Albandary AlBakheet, Sarah AlRuways, et al.
Cell|February 17, 2022
Mucosal fungi promote gut barrier function and social behavior via Type 17 immunityIrina Leonardi, Iris H Gao, Woan-Yu Lin, et al.
American Journal of Human Genetics|August 13, 2011
Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysmsLeen Abu-Safieh, Emad B Abboud, Hisham Alkuraya, et al.
Cell Stem Cell|July 13, 2010
Signaling through BMPR-IA regulates quiescence and long-term activity of neural stem cells in the adult hippocampusHelena Mira, Zoraida Andreu, Hoonkyo Suh, et al.
Cardiology|April 26, 2017
The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 MutationZarghuna M A Shinwari, Abdulrahman Almesned, Ali Alakhfash, et al.
Annals of Human Genetics|September 28, 2021
Genetics of ataxia telangiectasia in a highly consanguineous populationMohammed A Al-Muhaizea, Hanouf Aldeeb, Rawan Almass, et al.
Plos One|May 25, 2013
Age-specific gene expression signatures for breast tumors and cross-species conserved potential cancer progression markers in young womenDilek Colak, Asmaa Nofal, Albandary Albakheet, et al.
Genetic Testing and Molecular Biomarkers|December 17, 2021
Exome Sequencing Reveals Novel <i>TTN</i> Variants in Saudi Patients with Congenital TitinopathiesMustafa A Salih, Muddathir H Hamad, Marco Savarese, et al.
American Journal of Human Genetics|May 6, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen SyndromeNisha Patel, Hanan E Shamseldin, Nadia Sakati, et al.
Molecular Psychiatry|April 2, 2022
Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca<sup>2+</sup> signalingMegan Allen, Ben S Huang, Michael J Notaras, et al.
Pageof 15

Showing results (111-120 of 145) with videos related to

Sort By:
Pageof 15
Genes|January 21, 2022
A Novel <i>GEMIN4</i> Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and CataractsHesham Aldhalaan, Albandary AlBakheet, Sarah AlRuways, et al.
Cell|February 17, 2022
Mucosal fungi promote gut barrier function and social behavior via Type 17 immunityIrina Leonardi, Iris H Gao, Woan-Yu Lin, et al.
American Journal of Human Genetics|August 13, 2011
Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysmsLeen Abu-Safieh, Emad B Abboud, Hisham Alkuraya, et al.
Cell Stem Cell|July 13, 2010
Signaling through BMPR-IA regulates quiescence and long-term activity of neural stem cells in the adult hippocampusHelena Mira, Zoraida Andreu, Hoonkyo Suh, et al.
Cardiology|April 26, 2017
The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 MutationZarghuna M A Shinwari, Abdulrahman Almesned, Ali Alakhfash, et al.
Annals of Human Genetics|September 28, 2021
Genetics of ataxia telangiectasia in a highly consanguineous populationMohammed A Al-Muhaizea, Hanouf Aldeeb, Rawan Almass, et al.
Plos One|May 25, 2013
Age-specific gene expression signatures for breast tumors and cross-species conserved potential cancer progression markers in young womenDilek Colak, Asmaa Nofal, Albandary Albakheet, et al.
Genetic Testing and Molecular Biomarkers|December 17, 2021
Exome Sequencing Reveals Novel <i>TTN</i> Variants in Saudi Patients with Congenital TitinopathiesMustafa A Salih, Muddathir H Hamad, Marco Savarese, et al.
American Journal of Human Genetics|May 6, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen SyndromeNisha Patel, Hanan E Shamseldin, Nadia Sakati, et al.
Molecular Psychiatry|April 2, 2022
Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca<sup>2+</sup> signalingMegan Allen, Ben S Huang, Michael J Notaras, et al.
Pageof 15