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Imen Chakchouk

Showing results (1-10 of 25) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 1, 2026
Whole-Genome Amplification on Single Circulating Trophoblast CellImen Chakchouk, Ignatia B Van den Veyver
Prenatal Diagnosis|May 11, 2021
Overview and recent developments in cell-based noninvasive prenatal testingLiesbeth Vossaert, Imen Chakchouk, Roni Zemet, et al.
Genes|August 27, 2021
DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic ImprintingZahra Anvar, Imen Chakchouk, Hannah Demond, et al.
European Journal of Human Genetics : EJHG|May 5, 2019
Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestryImen Chakchouk, Di Zhang, Zhihui Zhang, et al.
BMC Medical Genetics|July 22, 2018
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Anushree Acharya, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|September 1, 2023
Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 SignalingZahra Anvar, Imen Chakchouk, Momal Sharif, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|March 28, 2023
Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1BZahra Anvar, Imen Chakchouk, Momal Sharif, et al.
The Journal of Molecular Diagnostics : JMD|January 7, 2015
NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countriesImen Chakchouk, Mariem Ben Said, Fida Jbeli, et al.
Journal of Biomolecular Structure & Dynamics|August 23, 2021
Molecular insights into <i>MYO3A</i> kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairmentAmal Souissi, Dorra Abdelmalek Driss, Imen Chakchouk, et al.
Human Genetics|July 5, 2018
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Khurram Liaqat, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

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Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|January 1, 2026
Whole-Genome Amplification on Single Circulating Trophoblast CellImen Chakchouk, Ignatia B Van den Veyver
Prenatal Diagnosis|May 11, 2021
Overview and recent developments in cell-based noninvasive prenatal testingLiesbeth Vossaert, Imen Chakchouk, Roni Zemet, et al.
Genes|August 27, 2021
DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic ImprintingZahra Anvar, Imen Chakchouk, Hannah Demond, et al.
European Journal of Human Genetics : EJHG|May 5, 2019
Disparities in discovery of pathogenic variants for autosomal recessive non-syndromic hearing impairment by ancestryImen Chakchouk, Di Zhang, Zhihui Zhang, et al.
BMC Medical Genetics|July 22, 2018
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Anushree Acharya, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|September 1, 2023
Comparison of Four Protocols for In Vitro Differentiation of Human Embryonic Stem Cells into Trophoblast Lineages by BMP4 and Dual Inhibition of Activin/Nodal and FGF2 SignalingZahra Anvar, Imen Chakchouk, Momal Sharif, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|March 28, 2023
Loss of the Maternal Effect Gene Nlrp2 Alters the Transcriptome of Ovulated Mouse Oocytes and Impacts Expression of Histone Demethylase KDM1BZahra Anvar, Imen Chakchouk, Momal Sharif, et al.
The Journal of Molecular Diagnostics : JMD|January 7, 2015
NADf chip, a two-color microarray for simultaneous screening of multigene mutations associated with hearing impairment in North African Mediterranean countriesImen Chakchouk, Mariem Ben Said, Fida Jbeli, et al.
Journal of Biomolecular Structure & Dynamics|August 23, 2021
Molecular insights into <i>MYO3A</i> kinase domain variants explain variability in both severity and progression of DFNB30 hearing impairmentAmal Souissi, Dorra Abdelmalek Driss, Imen Chakchouk, et al.
Human Genetics|July 5, 2018
A variant in LMX1A causes autosomal recessive severe-to-profound hearing impairmentIsabelle Schrauwen, Imen Chakchouk, Khurram Liaqat, et al.
Pageof 3