Annette Borchers

发表

The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled

J. Kashef, A. Merks, V. Bryja, 2020, Development.

Programming Pluripotent Precursor Cells Derived from Xenopus Embryos to Generate Specific Tissues and Organs

T. Pieler, A. Borchers, Annette Borchers, 2010, Genes.

Caveolin 1 is required for axonal outgrowth of motor neurons and affects Xenopus neuromuscular development

A. Borchers, Hanna Berger, Marlen Breuer, 2020, Scientific Reports.

The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish

K. Sampath, C. Y. Lim, N. R. Dunn, 2014, Development.

Using Xenopus to analyze neurocristopathies like Kabuki syndrome

A. Borchers, S. Pauli, Janina Schwenty-Lara, 2020, Genesis.

PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates

M. Tessier-Lavigne, J. Baker, H. Rayburn, 2004, Nature.

PTK7 Faces the Wnt in Development and Disease

A. Wodarz, A. Borchers, Hanna Berger, 2017, Front. Cell Dev. Biol..

PlexinA1 interacts with PTK7 and is required for neural crest migration.

G. Wagner, Hanna Peradziryi, A. Borchers, 2010, Biochemical and biophysical research communications.

PTK7 recruits dsh to regulate neural crest migration

I. Shnitsar, A. Borchers, Annette Borchers, 2008, Development.

Semaphorin and neuropilin expression during early morphogenesis of Xenopus laevis

A. Hufton, I. Shnitsar, A. Borchers, 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

The histone methyltransferase KMT2D, mutated in Kabuki syndrome patients, is required for neural crest cell formation and migration

A. Borchers, Janina Schwenty-Lara, D. Nehl, 2019, Human molecular genetics.

CHARGEd with neural crest defects

R. Bajpai, A. Borchers, S. Pauli, 2017, American journal of medical genetics. Part C, Seminars in medical genetics.

The many roles of PTK7: a versatile regulator of cell-cell communication.

N. Tolwinski, Hanna Peradziryi, A. Borchers, 2012, Archives of biochemistry and biophysics.

PTK7/Otk interacts with Wnts and inhibits canonical Wnt signalling

N. Tolwinski, Hanna Peradziryi, A. Borchers, 2011, The EMBO journal.

PTK7 localization and protein stability is affected by canonical Wnt ligands

R. Jacob, Hanna Peradziryi, A. Borchers, 2017, Journal of Cell Science.

The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development.

J. Baker, R. Harland, P. Jackson, 2002, Developmental biology.

An assay system to study migratory behavior of cranial neural crest cells in Xenopus

D. Wedlich, A. Borchers, H. Epperlein, 2000, Development Genes and Evolution.

Controlled levels of canonical Wnt signaling are required for neural crest migration.

T. Aspelmeier, T. Pieler, A. Borchers, 2016, Developmental biology.

A PTK7/Ror2 Co-Receptor Complex Affects Xenopus Neural Crest Migration

A. Borchers, Hanna Berger, M. Podleschny, 2015, PloS one.

The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs

J. Mackay, T. Stiewe, M. Mann, 2023, Nature Communications.

The H2A.Z.1/PWWP2A/NuRD-associated protein HMG20A controls early head and heart developmental transcription programs

J. Mackay, T. Stiewe, J. Leers, 2022, bioRxiv.

Ptk7 Is Dynamically Localized at Neural Crest Cell–Cell Contact Sites and Functions in Contact Inhibition of Locomotion

K. Giehl, A. Borchers, Anita Grund, 2021, International journal of molecular sciences.

Xenopus cadherin-11 restrains cranial neural crest migration and influences neural crest specification.

D. Wedlich, A. Borchers, R. David, 2001, Development.

Xenopus cadherin-11 (Xcadherin-11) expression requires the Wg/Wnt signal

D. Wedlich, A. Borchers, Beate Hadeball, 1998, Mechanisms of Development.

Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis

A. Borchers, Janina Schwenty-Lara, Annika Nürnberger, 2019, Developmental dynamics : an official publication of the American Association of Anatomists.

RACK1 is a novel interaction partner of PTK7 that is required for neural tube closure

H. Urlaub, I. Shnitsar, A. Borchers, 2011, Development.

De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome

M. Sturm, P. Nürnberg, J. Altmüller, 2020, Human Genetics.

CHD7, the gene mutated in CHARGE syndrome, regulates genes involved in neural crest cell guidance

E. Bongers, L. Opitz, J. Schoumans, 2014, Human Genetics.

XNF-ATc3 affects neural convergent extension

J. Baker, D. Frank, A. Borchers, 2006, Development.

The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish

K. Sampath, N. R. Dunn, Peter Wehner, 2014, Development.

The Rho GEF Trio is transported by microtubules and affects microtubule stability in migrating neural crest cells.

Stefanie Gossen, Sarah Gerstner, Annette Borchers, 2023, Cells & development.

Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome

Roser Ufartes, A. Borchers, S. Pauli, 2021, Frontiers in Cell and Developmental Biology.