S. Imreh

发表

Human wig-1, a p53 target gene that encodes a growth inhibitory zinc finger protein

C. Méndez-Vidal, K. Wiman, M. Kost-Alimova, 2001, Oncogene.

Chromosomal breaks during mitotic catastrophe trigger γH2AX–ATM–p53-mediated apoptosis

B. Zhivotovsky, S. Imreh, G. Imreh, 2011, Journal of Cell Science.

Sustained TGFβ exposure suppresses Smad and non-Smad signalling in mammary epithelial cells, leading to EMT and inhibition of growth arrest and apoptosis

T. Sjöblom, A. Moustakas, H. Beug, 2007, Oncogene.

Sustained TGF beta exposure suppresses Smad and non-Smad signalling in mammary epithelial cells, leading to EMT and inhibition of growth arrest and apoptosis.

T. Sjöblom, A. Moustakas, H. Beug, 2008, Oncogene.

Loss of Y in leukocytes, dysregulation of autosomal immune genes and disease risks

Behrooz Torabi Moghadam, A. Ameur, Stefan Enroth, 2019 .

CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.

A. Lindblom, L. Skoog, M. Kost-Alimova, 2005, International journal of molecular medicine.

Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients

G. Klein, M. Kost-Alimova, S. Imreh, 2006, European journal of haematology.

Jumping translocation of 17q11∼qter and 3q25∼q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia

G. Klein, M. Kost-Alimova, S. Imreh, 2006 .

Severe Defect in Thymic Development in an Insertional Mutant Mouse Model1

H. Ljunggren, S. Imreh, A. Grandien, 2007, The Journal of Immunology.

Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations.

G. Klein, M. Kost-Alimova, S. Imreh, 2007, Cancer genetics and cytogenetics.

Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene.

S. Imreh, D. David, G. Valentini, 2015, JIMD reports.

A minimal glycine-alanine repeat prevents the interaction of ubiquitinated I kappaB alpha with the proteasome: a new mechanism for selective inhibition of proteolysis.

M. Masucci, S. Imreh, A. Leonchiks, 1998, Nature medicine.

Mitotic infidelity and centrosome duplication errors in cells overexpressing tripeptidyl-peptidase II.

M. Masucci, M. Henriksson, S. Imreh, 2005, Cancer research.

Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues

U. Thorsteinsdóttir, J. Jónasson, S. Ingvarsson, 2004, Genes, chromosomes & cancer.

The EBV-encoded LMP1 protein inhibits p53-triggered apoptosis but not growth arrest.

Yi-Song Wang, G. Klein, K. Wiman, 1995, Oncogene.

Combined LOH/CGH analysis proves the existence of interstitial 3p deletions in renal cell carcinoma

Stefan Imreh, E. Zabarovsky, G. Klein, 2000, Oncogene.

Segmental duplications and evolutionary plasticity at tumor chromosome break-prone regions.

G. Klein, S. Müller, M. Kost-Alimova, 2008, Genome research.

Modeling non-random deletions in cancer.

M. Kost-Alimova, S. Imreh, M. Kost‐Alimova, 2007, Seminars in cancer biology.

Down regulation of 3p genes, LTF, SLC38A3 and DRR1, upon growth of human chromosome 3–mouse fibrosarcoma hybrids in severe combined immunodeficiency mice

G. Klein, M. Kost-Alimova, S. Imreh, 2006, International journal of cancer.

Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

Behrooz Torabi Moghadam, A. Ameur, Stefan Enroth, 2021, Cellular and Molecular Life Sciences.

Non-random genomic instability in cancer: a fact, not an illusion.

S. Imreh, S. Mai, 2007, Seminars in cancer biology.

Array-CGH and multipoint FISH to decode complex chromosomal rearrangements

G. Klein, T. de Ståhl, J. Dumanski, 2006, BMC Genomics.

Why do we not all die of cancer at an early age?

E. Zabarovsky, G. Klein, S. Imreh, 2007, Advances in cancer research.

Coincidence of synteny breakpoints with malignancy-related deletions on human chromosome 3

G. Klein, J. Dumanski, M. Kost-Alimova, 2003, Proceedings of the National Academy of Sciences of the United States of America.

The microcell hybrid‐based “elimination test” identifies a 1‐Mb putative tumor‐suppressor region at 3p22.2–p22.1 centromeric to the homozygous deletion region detected in lung cancer

G. Klein, M. Kost‐Alimova, S. Imreh, 2002, Genes, chromosomes & cancer.

Immune cells lacking Y chromosome have widespread dysregulation of autosomal genes

Behrooz Torabi Moghadam, J. Perry, A. Ameur, 2019, bioRxiv.

Inhibition of antigen processing by the internal repeat region of the EpsteinBarr virus nuclear antigen-1

Stefan Imreh, Michael Coram, G. Klein, 1995, Nature.

Insertional Mutant Mouse Model Severe Defect in Thymic Development in an

Fedorova Li, Hans-Gustaf Ljunggren, Benedict J. Chambers, 2013 .

A minimal glycine-alanine repeat prevents the interaction of ubiquitinated IκBα with the proteasome: a new mechanism for selective inhibition of proteolysis

Stefan Imreh, M. Masucci, S. Imreh, 1998, Nature Medicine.

B cell phenotype-dependent expression of the Epstein-Barr virus nuclear antigens EBNA-2 to EBNA-6: studies with somatic cell hybrids.

M. Masucci, S. Imreh, M. Anvret, 1991, The Journal of general virology.

E. Blennow, G. Gaidano, L. Andersson, 2002, AIDS research and human retroviruses.

Microcell‐mediated chromosome transfer provides evidence that polysomy promotes structural instability in tumor cell chromosomes through asynchronous replication and breakage within late‐replicating regions

G. Klein, M. Kost-Alimova, S. Imreh, 2004, Genes, chromosomes & cancer.

Culture and expansion of the human embryonic stem cell line HS181, evaluated in a double-color system.

S. Imreh, A. Aints, O. Hovatta, 2004, Stem cells and development.

BMC Cancer BioMed Central Research article Mandatory chromosomal segment balance in aneuploid tumor cells

Yue Cheng, Stefan Imreh, G. Klein, 2007 .

Consistent downregulation of human lactoferrin gene, in the common eliminated region 1 on 3p21.3, following tumor growth in severe combined immunodeficient (SCID) mice.

G. Klein, M. Kost-Alimova, S. Imreh, 2003, Cancer letters.

Jumping translocation of 17q11 approximately qter and 3q25 approximately q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous leukemia.

G. Klein, M. Kost-Alimova, S. Imreh, 2006, Cancer genetics and cytogenetics.

Organization, expression and polymorphism of the human persyn gene.

A. Davies, S. Imreh, V. Buchman, 1998, Human molecular genetics.

Array-CGH and multipoint FISH to decode complex chromosomal rearrangements.

G. Klein, J. Dumanski, M. Kost-Alimova, 2006 .

Chromosomal breaks during mitotic catastrophe trigger γH2AX–ATM–p53-mediated apoptosis

B. Zhivotovsky, S. Imreh, G. Imreh, 2016, Journal of Cell Science.

BMC Cancer BioMed Central Research article Mandatory chromosomal segment balance in aneuploid tumor cells

E. Stanbridge, S. Imreh, L. Fedorova, 2007 .