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ASPP2 maintains the integrity of mechanically stressed pseudostratified epithelia during morphogenesis

Journal article

Royer C. et al, (2022), Nature Communications, 13

Defect in Ser312 phosphorylation of Tp53 dysregulates lipid metabolism for fatty accumulation and fatty liver susceptibility: Revealed by lipidomics.

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He M. et al, (2022), Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1211

Mutant Ras and inflammation-driven skin tumorigenesis is suppressed via a JNK-iASPP-AP1 axis.

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Al Moussawi K. et al, (2022), Cell reports, 41

Multiscale Methods for Signal Selection in Single-Cell Data.

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Hoekzema RS. et al, (2022), Entropy (Basel, Switzerland), 24

Centriole distal-end proteins CP110 and Cep97 influence centriole cartwheel growth at the proximal-end

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Aydogan MG. et al, (2022), Journal of Cell Science

Factor inhibiting HIF can catalyze two asparaginyl hydroxylations in VNVN motifs of ankyrin fold proteins.

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Leissing TM. et al, (2022), The Journal of biological chemistry, 298

Deep Neural Network Based Inertial Odometry Using Low-Cost Inertial Measurement Units

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Chen C. et al, (2021), IEEE Transactions on Mobile Computing, 20, 1351 - 1364

A deep learning framework for quality assessment and restoration in video endoscopy

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Ali S. et al, (2021), Medical Image Analysis, 68, 101900 - 101900

Arsenic Trioxide Rescues Structural p53 Mutations through a Cryptic Allosteric Site

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Chen S. et al, (2021), Cancer Cell, 39, 225 - 239.e8

Tuning Transcription Factor Availability through Acetylation-Mediated Genomic Redistribution

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Louphrasitthiphol P. et al, (2020), Molecular Cell, 79, 472 - 487.e10

CagA–ASPP2 complex mediates loss of cell polarity and favors H. pylori colonization of human gastric organoids

Journal article

Buti L. et al, (2020), Proceedings of the National Academy of Sciences, 117, 2645 - 2655

iASPP mediates p53 selectivity through a modular mechanism fine-tuning DNA recognition

Journal article

Chen S. et al, (2019), Proceedings of the National Academy of Sciences, 116, 17470 - 17479

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.

Journal article

O'Donnell-Luria AH. et al, (2019), American journal of human genetics, 104, 1210 - 1222

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