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Matthew Guille

Showing results (21-30 of 29) with videos related to

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Journal of Leukocyte Biology|June 24, 2017
Adipose tissue macrophages develop from bone marrow-independent progenitors in <i>Xenopus laevis</i> and mouseSyed F Hassnain Waqas, Anna Noble, Anh C Hoang, et al.
Developmental Biology|December 30, 2021
An efficient miRNA knockout approach using CRISPR-Cas9 in XenopusAlice M Godden, Marco Antonaci, Nicole J Ward, et al.
Frontiers in Physiology|May 11, 2019
<i>Xenopus</i> Resources: Transgenic, Inbred and Mutant Animals, Training Opportunities, and Web-Based SupportMarko Horb, Marcin Wlizla, Anita Abu-Daya, et al.
Cell Death Discovery|December 19, 2025
Novel mutations in the RECQL4 gene affect its helicase functions, interactions with the BLM helicase and chemotherapeutics-induced cell deathAgnieszka Kaczmarczyk, Mikolaj Sokolowski, Kamil Wojnicki, et al.
Genome Medicine|February 26, 2021
Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephalyWilliam L Macken, Annie Godwin, Gabrielle Wheway, et al.
American Journal of Human Genetics|June 8, 2022
Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndromeVardha Ismail, Linda G Zachariassen, Annie Godwin, et al.
American Journal of Human Genetics|February 29, 2020
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental DisordersSónia Barbosa, Stephanie Greville-Heygate, Maxime Bonnet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2026
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological InvolvementValentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
Brain : a Journal of Neurology|November 11, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disordersRauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, et al.
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Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Journal of Leukocyte Biology|June 24, 2017
Adipose tissue macrophages develop from bone marrow-independent progenitors in <i>Xenopus laevis</i> and mouseSyed F Hassnain Waqas, Anna Noble, Anh C Hoang, et al.
Developmental Biology|December 30, 2021
An efficient miRNA knockout approach using CRISPR-Cas9 in XenopusAlice M Godden, Marco Antonaci, Nicole J Ward, et al.
Frontiers in Physiology|May 11, 2019
<i>Xenopus</i> Resources: Transgenic, Inbred and Mutant Animals, Training Opportunities, and Web-Based SupportMarko Horb, Marcin Wlizla, Anita Abu-Daya, et al.
Cell Death Discovery|December 19, 2025
Novel mutations in the RECQL4 gene affect its helicase functions, interactions with the BLM helicase and chemotherapeutics-induced cell deathAgnieszka Kaczmarczyk, Mikolaj Sokolowski, Kamil Wojnicki, et al.
Genome Medicine|February 26, 2021
Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephalyWilliam L Macken, Annie Godwin, Gabrielle Wheway, et al.
American Journal of Human Genetics|June 8, 2022
Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndromeVardha Ismail, Linda G Zachariassen, Annie Godwin, et al.
American Journal of Human Genetics|February 29, 2020
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental DisordersSónia Barbosa, Stephanie Greville-Heygate, Maxime Bonnet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2026
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological InvolvementValentina Galassi Deforie, Reza Maroofian, Irem Karagoz, et al.
Brain : a Journal of Neurology|November 11, 2023
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disordersRauan Kaiyrzhanov, Aboulfazl Rad, Sheng-Jia Lin, et al.
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