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Annette Borchers

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

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Disease Models & Mechanisms|November 24, 2025
Fbrsl1 is required for cranial neural crest development and reflects a conserved function of the human disease-associated proteinSarah Gerstner, Hanna Berger-Santangelo, Gina Kastens, et al.
Human Genetics|July 14, 2025
FBRSL1 regulates the expression of chromatin regulators BRPF1 and KAT6AGina Kastens, Hanna Berger-Santangelo, Sarah Gerstner, et al.
The EMBO Journal|July 21, 2011
PTK7/Otk interacts with Wnts and inhibits canonical Wnt signallingHanna Peradziryi, Nicole A Kaplan, Martina Podleschny, et al.
Developmental Biology|June 26, 2016
Controlled levels of canonical Wnt signaling are required for neural crest migrationEwa Maj, Lutz Künneke, Elisabeth Loresch, et al.
Development (Cambridge, England)|May 6, 2020
The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with DishevelledMarie-Claire Kratzer, Sarah F S Becker, Anita Grund, et al.
Human Genetics|May 20, 2020
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndromeRoser Ufartes, Hanna Berger, Katharina Till, et al.
Human Genetics|April 15, 2014
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidanceYvonne Schulz, Peter Wehner, Lennart Opitz, et al.
Human Molecular Genetics|February 13, 2018
Sema3a plays a role in the pathogenesis of CHARGE syndromeRoser Ufartes, Janina Schwenty-Lara, Luisa Freese, et al.
Development (Cambridge, England)|September 4, 2014
The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafishTeddy Young, Yogavalli Poobalan, Ee Kim Tan, et al.
Nature Communications|January 28, 2023
The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programsAndreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
Pageof 3

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

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Disease Models & Mechanisms|November 24, 2025
Fbrsl1 is required for cranial neural crest development and reflects a conserved function of the human disease-associated proteinSarah Gerstner, Hanna Berger-Santangelo, Gina Kastens, et al.
Human Genetics|July 14, 2025
FBRSL1 regulates the expression of chromatin regulators BRPF1 and KAT6AGina Kastens, Hanna Berger-Santangelo, Sarah Gerstner, et al.
The EMBO Journal|July 21, 2011
PTK7/Otk interacts with Wnts and inhibits canonical Wnt signallingHanna Peradziryi, Nicole A Kaplan, Martina Podleschny, et al.
Developmental Biology|June 26, 2016
Controlled levels of canonical Wnt signaling are required for neural crest migrationEwa Maj, Lutz Künneke, Elisabeth Loresch, et al.
Development (Cambridge, England)|May 6, 2020
The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with DishevelledMarie-Claire Kratzer, Sarah F S Becker, Anita Grund, et al.
Human Genetics|May 20, 2020
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndromeRoser Ufartes, Hanna Berger, Katharina Till, et al.
Human Genetics|April 15, 2014
CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidanceYvonne Schulz, Peter Wehner, Lennart Opitz, et al.
Human Molecular Genetics|February 13, 2018
Sema3a plays a role in the pathogenesis of CHARGE syndromeRoser Ufartes, Janina Schwenty-Lara, Luisa Freese, et al.
Development (Cambridge, England)|September 4, 2014
The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafishTeddy Young, Yogavalli Poobalan, Ee Kim Tan, et al.
Nature Communications|January 28, 2023
The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programsAndreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
Pageof 3