Verbinnen Iris - From the Laboratory of Biosignaling & Therapeutics, University of Leuven

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论文共 23 篇作者统计合作学者相似作者

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PPP2R5E: New Gene Potentially Involved in Specific Learning Disorders and Myopathy

Antonino Musumeci,Mirella Vinci,Iris Verbinnen,Simone Treccarichi, Eleonora Nigliato,Valeria Chiavetta,Donatella Greco,Girolamo Aurelio Vitello,Concetta Federico,Veerle Janssens, Salvatore Saccone, Francesco Cali

GENE (2025)

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Embryonic NIPP1 Depletion in Keratinocytes Triggers a Cell Cycle Arrest and Premature Senescence in Adult Mice

Marloes C. M. Jonkhout, Tijs Vanhessche,Monica Ferreira,Iris Verbinnen, Fabienne Withof,Gerd van der Hoeven,Kathelijne Szeker, Zahra Azhir,Wen-Hui Lien,Aleyde Van Eynde,Mathieu Bollen

JOURNAL OF INVESTIGATIVE DERMATOLOGY（2024）

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Elevating the Standard of Care for Patients with Psoriatic Arthritis: 'calls to Action' from a Multistakeholder Pan-European Initiative

Iris Verbinnen,Emilio Monte-Boquet, Detlev Parow, Fabienne Lacombe, Andrew Pothecary,Arno W. R. van Kuijk, Laura Harrington, Edita Müllerová,Andreas Pinter,Ulrike Erstling, Andrea Tomasini,Philip S. Helliwell

RHEUMATOLOGY AND THERAPYno. 3 (2024): 795-815

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The role of liprin-α1 phosphorylation in its liquid-liquid phase separation: regulation by PPP2R5D/PP2A holoenzyme

Abigail Mayer,Rita Derua, Elijah Spahn,Iris Verbinnen, Yang Zhang,Brian Wadzinski,Mark R Swingle,Richard Honkanen,Veerle Janssens,Houhui Xia

bioRxiv : the preprint server for biology (2024)

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A Novel Mouse Model of Combined Hepatocellular-Cholangiocarcinoma Induced by Diethylnitrosamine and Loss of Ppp2r5d

Judit Domenech Omella,Emanuela E. Cortesi,Iris Verbinnen,Michiel Remmerie,Hanghang Wu,Francisco J. Cubero,Tania Roskams,Veerle Janssens

CANCERS（2023）

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Characterization of de novo variants in PPP2R5C expands the spectrum of PP2A-related neurodevelopmental disorders

Iris Verbinnen,Elise Brimble,Lisa Lenaerts,David Genevieve,Laurence Faivre,Julien Thevenon,Jessica X. Chong,Mike Bamshad,Karynne Patterson,Elysa Marco,Dmitriy Niyazov,Aida Telegrafi,Sumit Punj,Kimberly Foss,William Dobyns, Ghaydda Mirzaa,Chin-To Fong,Sue White,Lynn Pais,Emily O'Heir,Celia van der Merwe,Raphaela Itzikowitz,Kirsty Donald,Tony Roscioli, Kerith-Rae Dias,Carey-Anne Evans,Alessandro Mussa, Raffaela Cervini,Elisa Giorgio,Anna Ruiz, Juan Pablo Trujillo Quintero,Rachel Rabin,John Pappas,Xiaodong Wang, J. Wang, Hua Yuan,Maura R. Z. Ruzhnikov,Veerle Janssens

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 451-452

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Clinical and Molecular Characteristics of a Novel Rare De Novo Variant in PPP2CA in a Patient with a Developmental Disorder, Autism, and Epilepsy

Iris Verbinnen,Sara S. S. Procknow,Lisa Lenaerts,Sara Reynhout,Aujan Mehregan,Chris Ulens,Veerle Janssens,Katherine A. A. King

Frontiers in Cell and Developmental Biology（2022）

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The Role of Serine/threonine Phosphatases in Human Development: Evidence from Congenital Disorders

Pieter Vaneynde,Iris Verbinnen,Veerle Janssens

Frontiers in Cell and Developmental Biology（2022）

引用5浏览0引用

Protein Phosphatase 2A (PP2A) Mutations in Brain Function, Development, and Neurologic Disease

Iris Verbinnen,Pieter Vaneynde,Sara Reynhout,Lisa Lenaerts,Rita Derua,Gunnar Houge,Veerle Janssens

Biochemical Society Transactions（2021）

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The Broad Phenotypic Spectrum of PPP2R1A -Related Neurodevelopmental Disorders Correlates with the Degree of Biochemical Dysfunction

Genetics in medicine（2021）

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