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The Hippo pathway component Wwc2 is a key regulator of embryonic development and angiogenesis in mice2021 Cell Death and Disease article Biochemistry, Genetics and Molecular Biology Hippo pathway signaling and YAP/TAZ Open access
Anke Hermann, Guangming Wu, Pavel I. Nedvetsky, Viktoria Constanze Brücher, Charlotte Egbring, Jakob Bonse, +8 more
35citations -
Dynamics of Size and Shape Variation During Embryonic Development in the Balkan Crested Newt2026 Journal of Experimental Zoology Part B Molecular and Developmental Evolution article Mathematics Morphological variations and asymmetry Open access
Marko Bugarčić, Ana Ivanović, Milena Cvijanović, Maja Ajduković, Ben Wielstra, Tijana Z. Vučić
0citations -
A staging table of Balkan crested newt embryonic development to serve as a baseline in evolutionary developmental studies2024 Journal of Experimental Zoology Part B Molecular and Developmental Evolution article Biochemistry, Genetics and Molecular Biology Developmental Biology and Gene Regulation Open access
Tijana Z. Vučić, Maja Ajduković, Marko Bugarčić, Ben Wielstra, Ana Ivanović, Milena Cvijanović
7citations -
Epicardial Abnormalities and Mesenchymal/Hematopoietic Cell Expansion in Plakophilin 2-Null Mouse Embryonic Hearts2025 Cells article Biochemistry, Genetics and Molecular Biology Congenital heart defects research Open access
Mistura Dolapo Bolaji, P. E. Hartmann, Eva Miriam Buhl, Robin M. W. Colpaert, Francesca Gasparella, León J. De Windt, +3 more
0citations -
A BRCA1 Coiled-Coil Domain Variant Disrupting PALB2 Interaction Promotes the Development of Mammary Tumors and Confers a Targetable Defect in Homologous Recombination Repair2021 Cancer Research article Biochemistry, Genetics and Molecular Biology BRCA gene mutations in cancer Open access
Emilia M. Pulver, Chirantani Mukherjee, Gerarda van de Kamp, Stefan J. Roobol, Magdalena B. Rother, Hanneke van der Gulden, +18 more
20citations -
Data from A BRCA1 Coiled-Coil Domain Variant Disrupting PALB2 Interaction Promotes the Development of Mammary Tumors and Confers a Targetable Defect in Homologous Recombination Repair
Emilia M. Pulver, Chirantani Mukherjee, Gerarda van de Kamp, Stefan J. Roobol, Magdalena B. Rother, Hanneke van der Gulden, +18 more
0citations -
Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot2021 Genetics in Medicine article Biochemistry, Genetics and Molecular Biology Congenital heart defects research Open access
Doris Škorić‐Milosavljević, Najim Lahrouchi, Fernanda M. Bosada, Gregor Dombrowsky, Simon G. Williams, Robert Lesurf, +48 more
18citations -
The Evolutionary Conserved Transmembrane BAX Inhibitor Motif (TMBIM) Containing Protein Family Members 5 and 6 Are Essential for the Development and Survival of Drosophila melanogaster5citations
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Left–Right Reversal Recurrently Evolved Regardless of Diaphanous-Related Formin Gene Duplication or Loss in Snails2023 Journal of Molecular Evolution article Biochemistry, Genetics and Molecular Biology Developmental Biology and Gene Regulation Open access
Takeshi Noda, Noriyuki Satoh, Edmund Gittenberger, Takahiro Asami
1citations -
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA32024 The American Journal of Human Genetics article Biochemistry, Genetics and Molecular Biology Genetics and Neurodevelopmental Disorders Open access
Maimuna Sali Paul, Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill Anne Rosenfeld, +94 more
16citations -
PAV-spotter: using signal cross-correlations to identify Presence/Absence Variation in target capture data2024 bioRxiv (Cold Spring Harbor Laboratory) preprint Biochemistry, Genetics and Molecular Biology Genomics and Phylogenetic Studies Open access
Manon Chantal de Visser, Chris van der Ploeg, Milena Cvijanović, Tijana Z. Vučić, Anagnostis Theodoropoulos, Ben Wielstra
4citations -
Desmoglein 2 regulates cardiogenesis by restricting hematopoiesis in the developing murine heart2021 Scientific Reports article Biochemistry, Genetics and Molecular Biology Congenital heart defects research Open access
Hoda Moazzen, Kateryna Venger, Sebastian Kant, Rudolf E. Leube, Claudia A. Krusche
9citations -
CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout2022 Stem Cell Research article Biochemistry, Genetics and Molecular Biology Pluripotent Stem Cells Research Open access
Marcelo A. S. Toledo, Xu‐Huang Fu, Frederick Kluge, Katrin Götz, Susanne Schmitz, Paul Wanek, +6 more
2citations -
Mechanisms of Podocyte Injury Due to Loss of the Nucleoporin NUP932025 Journal of the American Society of Nephrology article Medicine Renal Diseases and Glomerulopathies Open access
Hussein Bachir, Vanessa Krausel, Florian Buerger, Mohamed Hamed, Barbara Heitplatz, Veerle Van Marck, +11 more
1citations -
Editorial: Protein post-translational modifications in the nervous system: from development to disease and ageing2024 Frontiers in Molecular Neuroscience editorial Medicine Alzheimer's disease research and treatments Open access
Judit Symmank, Geraldine Zimmer‐Bensch, Miguel Dı́az-Hernández, Patricia Franzka
1citations -
P-802 Unraveling a distinct role for GATA3 in mouse and human trophectoderm development via CRISPR/Cas9 gene editing2025 Human Reproduction conference-abstract Biochemistry, Genetics and Molecular Biology Pluripotent Stem Cells Research Open access
Sofie Declercq, Gwenny Cosemans, Tijs Vanhessche, Dominic Stoop, Susana M. Chuva de Sousa Lopes, Kim De Leeneer, +2 more
0citations
19 results