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Arzu Celik

Showing results (11-20 of 20) with videos related to

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Nature|June 21, 2013
Temporal patterning of Drosophila medulla neuroblasts controls neural fatesXin Li, Ted Erclik, Claire Bertet, et al.
Omics : a Journal of Integrative Biology|April 16, 2019
Identification of Novel Components of Target-of-Rapamycin Signaling Pathway by Network-Based Multi-Omics Integrative AnalysisElif Dereli Eke, Kazim Yalcin Arga, Duygu Dikicioglu, et al.
Plos Biology|April 25, 2008
Iroquois complex genes induce co-expression of rhodopsins in DrosophilaEsteban O Mazzoni, Arzu Celik, Mathias F Wernet, et al.
Nature|October 11, 2011
Feedback from rhodopsin controls rhodopsin exclusion in Drosophila photoreceptorsDaniel Vasiliauskas, Esteban O Mazzoni, Simon G Sprecher, et al.
Cell Reports|December 24, 2014
Mapping gene regulatory networks in Drosophila eye development by large-scale transcriptome perturbations and motif inferenceDelphine Potier, Kristofer Davie, Gert Hulselmans, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 20, 2018
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disabilitySomayeh Kazeminasab, Ibrahim Ihsan Taskiran, Zohreh Fattahi, et al.
Archives of Iranian Medicine|July 1, 2021
<i>CEP104</i> and <i>CEP290</i>; Genes with Ciliary Functions Cause Intellectual Disability in Multiple FamiliesShahrouz Khoshbakht, Maryam Beheshtian, Zohreh Fattahi, et al.
The European Journal of Neuroscience|January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapsesRobert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Molecular Biology of the Cell|December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleusHeike Laser, Laura Conforti, Giacomo Morreale, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Nature|June 21, 2013
Temporal patterning of Drosophila medulla neuroblasts controls neural fatesXin Li, Ted Erclik, Claire Bertet, et al.
Omics : a Journal of Integrative Biology|April 16, 2019
Identification of Novel Components of Target-of-Rapamycin Signaling Pathway by Network-Based Multi-Omics Integrative AnalysisElif Dereli Eke, Kazim Yalcin Arga, Duygu Dikicioglu, et al.
Plos Biology|April 25, 2008
Iroquois complex genes induce co-expression of rhodopsins in DrosophilaEsteban O Mazzoni, Arzu Celik, Mathias F Wernet, et al.
Nature|October 11, 2011
Feedback from rhodopsin controls rhodopsin exclusion in Drosophila photoreceptorsDaniel Vasiliauskas, Esteban O Mazzoni, Simon G Sprecher, et al.
Cell Reports|December 24, 2014
Mapping gene regulatory networks in Drosophila eye development by large-scale transcriptome perturbations and motif inferenceDelphine Potier, Kristofer Davie, Gert Hulselmans, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 20, 2018
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disabilitySomayeh Kazeminasab, Ibrahim Ihsan Taskiran, Zohreh Fattahi, et al.
Archives of Iranian Medicine|July 1, 2021
<i>CEP104</i> and <i>CEP290</i>; Genes with Ciliary Functions Cause Intellectual Disability in Multiple FamiliesShahrouz Khoshbakht, Maryam Beheshtian, Zohreh Fattahi, et al.
The European Journal of Neuroscience|January 19, 2005
A rat model of slow Wallerian degeneration (WldS) with improved preservation of neuromuscular synapsesRobert Adalbert, Thomas H Gillingwater, Jane E Haley, et al.
Molecular Biology of the Cell|December 24, 2005
The slow Wallerian degeneration protein, WldS, binds directly to VCP/p97 and partially redistributes it within the nucleusHeike Laser, Laura Conforti, Giacomo Morreale, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
Pageof 2