Idan Cohen

发表

A Deletion Mutation in TMEM38B Associated with Autosomal Recessive Osteogenesis Imperfecta

D. Landau, O. Birk, B. Markus, 2013, Human mutation.

Association analysis identifies ZNF750 regulatory variants in psoriasis

P. Kwok, O. Birk, W. Liao, 2011, BMC Medical Genetics.

Polycomb complexes redundantly maintain epidermal stem cell identity during development

D. Zheng, Jose M. Silva, Dejian Zhao, 2021, Genes & development.

Polycomb-Mediated Repression and Sonic Hedgehog Signaling Interact to Regulate Merkel Cell Specification during Skin Development

D. Zheng, Francis J. Santoriello, Dejian Zhao, 2016, PLoS genetics.

RSRC1 mutation affects intellect and behaviour through aberrant splicing and transcription, downregulating IGFBP3

Esti Yeger-Lotem, R. Ofir, O. Birk, 2018, Brain : a journal of neurology.

Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.

O. Birk, B. Markus, I. Shelef, 2010, American journal of human genetics.

Polycomb Repressive Complex 1 Controls Maintenance of Fungiform Papillae by Repressing Sonic Hedgehog Expression

D. Zheng, V. Pothula, Dejian Zhao, 2019, Cell reports.

PRC1 Fine-tunes Gene Repression and Activation to Safeguard Skin Development and Stem Cell Specification.

D. Zheng, W. Bickmore, Dejian Zhao, 2018, Cell stem cell.

Polycomb Repressive Complex(es) and Their Role in Adult Stem Cells

E. Ezhkova, Idan Cohen, P. Flora, 2021, Genes.

Activity of PRC1 and Histone H2AK119 Monoubiquitination: Revising Popular Misconceptions

E. Ezhkova, Idan Cohen, Carmit Bar, 2020, BioEssays : news and reviews in molecular, cellular and developmental biology.

Polycomb Proteins and their Roles in Skin Development and Regeneration

E. Ezhkova, Idan Cohen, Katherine L. Dauber-Decker, 2018 .

ALFY-Controlled DVL3 Autophagy Regulates Wnt Signaling, Determining Human Brain Size

O. Birk, B. Markus, T. Harel, 2016, PLoS genetics.

MEK1/2 inhibition transiently alters the tumor immune microenvironment to enhance immunotherapy efficacy against head and neck cancer

Y. Carmi, A. Mock, J. Hess, 2021, Journal for ImmunoTherapy of Cancer.

Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase

G. Narkis, D. Landau, K. Elbedour, 2013, European Journal of Human Genetics.

Epigenetic regulation and signalling pathways in Merkel cell development

Idan Cohen, L. Oss-Ronen, Idan Cohen, 2021, Experimental dermatology.

PRC1 preserves epidermal tissue integrity independently of PRC2

D. Zheng, Dejian Zhao, H. Koseki, 2018, Genes & development.

FGF signalling controls the specification of hair placode-derived SOX9 positive progenitors to Merkel cells

O. Klein, M. Mikkola, Y. Hsu, 2018, Nature Communications.

Dissecting the Roles of Polycomb Repressive Complex 2 Subunits in the Control of Skin Development.

Francis J. Santoriello, E. Ezhkova, Idan Cohen, 2016, The Journal of investigative dermatology.

Cbx4: A new guardian of p63’s domain of epidermal control

E. Ezhkova, Idan Cohen, Idan Cohen, 2016, The Journal of cell biology.

UV-induced reduction in Polycomb repression promotes epidermal pigmentation.

D. Zheng, Jose M. Silva, J. D'Orazio, 2021, Developmental cell.

Epigenetic gene regulation, chromatin structure, and force-induced chromatin remodelling in epidermal development and homeostasis.

S. Wickström, E. Ezhkova, Idan Cohen, 2019, Current opinion in genetics & development.

Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1

G. Narkis, D. Landau, O. Birk, 2012, Human mutation.

Controlled assembly of perovskite nanoparticles by photoswitchable functional ligands

L. Etgar, Tal Binyamin, Orit Cohen, 2023, Journal of Physics: Energy.

X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome

O. Birk, A. Nahum, R. Schreiber, 2023, European Journal of Human Genetics.

Histone Mono-Ubiquitination in Transcriptional Regulation and Its Mark on Life: Emerging Roles in Tissue Development and Disease

Idan Cohen, L. Oss-Ronen, Tzlil Sarusi, 2022, Cells.

Meconium ileus caused by mutations in GUCY2C, encoding the CFTR-activating guanylate cyclase 2C.

Rivka Ofir, Idan Cohen, D. Landau, 2012, American journal of human genetics.

A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansion

O. Birk, Ann Saada, Y. Perez, 2017, American journal of medical genetics. Part A.

ZNF750 Is Expressed in Differentiated Keratinocytes and Regulates Epidermal Late Differentiation Genes

O. Birk, R. Taube, R. Birnbaum, 2012, PloS one.

VPS53 mutations cause progressive cerebello-cerebral atrophy type 2 (PCCA2)

E. Leshinsky‐Silver, D. Lev, O. Birk, 2014, Journal of Medical Genetics.

Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation

O. Birk, B. Markus, Y. Perez, 2013, European Journal of Human Genetics.

Functional Blood Progenitor Markers in Developing Human Liver Progenitors

V. Gouon-Evans, Orit Goldman, Idan Cohen, 2016, Stem cell reports.

Dissection of Merkel cell formation in hairy and glabrous skin reveals a common requirement for FGFR2‐mediated signalling

D. Zheng, V. Pothula, Dejian Zhao, 2019, Experimental dermatology.