S. Selig

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The Gag Cleavage Product, p12, is a Functional Constituent of the Murine Leukemia Virus Pre-Integration Complex

M. Ehrlich, Adi Prizan-Ravid, Efrat Elis, 2010, PLoS pathogens.

HLA B*5701 is highly associated with restriction of virus replication in a subgroup of HIV-infected long term nonprogressors.

F. Marincola, C. Hallahan, S. Migueles, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Y chromosomes of Jewish priests

M. Hammer, N. Bradman, K. Skorecki, 1997, Nature.

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

S. Rosset, N. Bradman, E. Bekele, 2010, Human Genetics.

News you can use

H. Cedar, I. Keshet, S. Selig, 1993, Nature.

Replication structure of the human & beta;-globin gene domain

H. Cedar, I. Keshet, I. Keshet, 1993, Nature.

Persistent epigenetic memory impedes rescue of the telomeric phenotype in human ICF iPSCs following DNMT3B correction

M. Gagliardi, M. R. Matarazzo, M. Tzukerman, 2019, eLife.

DNA:RNA hybrids at telomeres – when it is better to be out of the (R) loop

S. Selig, Shir Toubiana, 2018, The FEBS journal.

HIV envelope induces a cascade of cell signals in non-proliferating target cells that favor virus replication

Richard A Lempicki, Douglas A. Hosack, Anthony S Fauci, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Induced pluripotent stem cells as a model for telomeric abnormalities in ICF type I syndrome.

D. Geiger, M. Tzukerman, S. Selig, 2014, Human molecular genetics.

Hypomethylation of subtelomeric regions in ICF syndrome is associated with abnormally short telomeres and enhanced transcription from telomeric regions.

Y. Segev, K. Skorecki, S. Selig, 2008, Human molecular genetics.

Dp140: a novel 140 kDa CNS transcript from the dystrophin locus.

L. Kunkel, H. Lidov, S. Selig, 1995, Human molecular genetics.

The rescue of epigenomic abnormalities in ICF1 patient iPSCs following DNMT3B correction is incomplete at a residual fraction of H3K4me3-enriched regions

C. Angelini, M. Strazzullo, M. R. Matarazzo, 2022, bioRxiv.

Epigenetic Characteristics of Human Subtelomeres Vary in Cells Utilizing the Alternative Lengthening of Telomeres (ALT) Pathway

S. Selig, Shir Toubiana, Aya Tzur-Gilat, 2021, Life.

Regulation of telomeric function by DNA methylation differs between humans and mice.

S. Selig, L. Godley, C. Francastel, 2020, Human molecular genetics.

Human subtelomeric DNA methylation: regulation and roles in telomere function.

S. Selig, Shir Toubiana, 2020, Current opinion in genetics & development.

Allelic inactivation of rDNA loci.

H. Cedar, Y. Bergman, S. Selig, 2009, Genes & development.

HIV-1 envelope induces activation of caspase-3 and cleavage of focal adhesion kinase in primary human CD4(+) T cells.

C. Cicala, J. Arthos, S. Selig, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

G. Penchaszadeh, T. Carter, E. Vitale, 1995, American journal of human genetics.

Quantitative digital in situ senescence-associated β-galactosidase assay

S. Itzkovitz, A. Cohen, K. Skorecki, 2011, BMC Cell Biology.

Biochemical and Biological Characterization of a Dodecameric CD4-Ig Fusion Protein

T. Chun, A. Fauci, C. Cicala, 2002, The Journal of Biological Chemistry.

Early Response to Highly Active Antiretroviral Therapy in HIV-1-Infected Kenyan Children

J. Overbaugh, B. Richardson, S. Selig, 2007, Journal of acquired immune deficiency syndromes.

Delineation of DNA replication time zones by fluorescence in situ hybridization.

D. Ward, H. Cedar, S. Selig, 1992, The EMBO journal.

Synchronous and Asynchronous Replication

S. Selig, 2006 .

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects

I. Barshack, E. Eyal, N. Amariglio, 2016, The Journal of experimental medicine.

Digital image analysis of cells stained with the senescence-associated β-galactosidase assay.

S. Selig, L. Shlush, 2013, Methods in molecular biology.

A case for diagnosis

O. Sarig, E. Sprecher, S. Selig, 2015, Clinical and experimental dermatology.

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.

L. Kunkel, T. Gilliam, J. Scharf, 1995, Proceedings of the National Academy of Sciences of the United States of America.

MBTPS1 regulates proliferation of colorectal cancer primarily through its action on sterol regulatory element-binding proteins

S. Selig, Maya Lalzar, Shir Toubiana, 2022, Frontiers in Oncology.

Allele-specific replication timing of imprinted gene regions

D. J. Driscoll, I. Simon, H. Cedar, 1993, Nature.

Non-random length distribution of individual telomeres in immunodeficiency, centromeric instability and facial anomalies syndrome, type I

I. Bar-Am, S. Selig, T. Kozlovski, 2017, Human molecular genetics.

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

D. Magen, K. Skorecki, S. Selig, 2010, The New England journal of medicine.

Immune Responses to Measles and Tetanus Vaccines Among Kenyan Human Immunodeficiency Virus Type 1 (HIV-1)-Infected Children Pre- and Post-Highly Active Antiretroviral Therapy and Revaccination

N. Haigwood, S. Selig, G. John-Stewart, 2009, The Pediatric infectious disease journal.

Characterization and rescue of telomeric abnormalities in ICF syndrome type I fibroblasts

Y. Segev, S. Selig, Hofit Shachar-Bener, 2013, Front. Oncol..

Molecular characterization of Br-cadherin, a developmentally regulated, brain-specific cadherin.

L. Kunkel, M. Segal, H. Lidov, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Telomere elongation followed by telomere length reduction, in leukocytes from divers exposed to intense oxidative stress – Implications for tissue and organismal aging

S. Itzkovitz, P. Lansdorp, Y. Segev, 2011, Mechanisms of Ageing and Development.

Position effect of human telomeric repeats on replication timing.

K. Skorecki, H. McDermid, A. Wong, 1999, Proceedings of the National Academy of Sciences of the United States of America.

The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males

J. Beckmann, D. Hamer, D. Lancet, 2006, Human Genetics.

Reprogramming of telomeric regions during the generation of human induced pluripotent stem cells and subsequent differentiation into fibroblast-like derivatives

Y. Segev, K. Skorecki, L. Gepstein, 2011, Epigenetics.

African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic Americans

S. Rosset, D. Behar, C. Winkler, 2010, Human molecular genetics.

Regulation of Murine Telomere Length by Rtel An Essential Gene Encoding a Helicase-like Protein

P. Lansdorp, S. Poon, P. Tam, 2004, Cell.

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome

S. Selig, A. Kaindl, C. Francastel, 2018, Human molecular genetics.

Replication and/or separation of some human telomeres is delayed beyond S-phase in pre-senescent cells

Y. Segev, K. Skorecki, S. Selig, 2002, Chromosoma.

Sister chromatid separation at human telomeric regions

Y. Segev, K. Skorecki, M. Yalon, 2004, Journal of Cell Science.

Telomeres and Telomerase in Human Health and Disease

K. Skorecki, M. Tzukerman, S. Selig, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Chromosome structure and eukaryotic gene organization.

H. Cedar, S. Selig, D. Kitsberg, 1991, Current opinion in genetics & development.

Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation

Y. Zhang, Harinder Singh, S. Selig, 2010, PloS one.

Medication diaries do not improve outcomes with highly active antiretroviral therapy in Kenyan children: a randomized clinical trial

J. Overbaugh, B. Richardson, S. Selig, 2009, Journal of the International AIDS Society.

Regulation of mouse satellite DNA replication time.

H. Cedar, S. Selig, M. Marcus, 1988, The EMBO journal.

RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function

K. Weiss, A. Mory, S. Selig, 2021, Journal of Human Genetics.

Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids

F. Chédin, S. Selig, C. Francastel, 2017, Nature Communications.

Biochemical and Biological Characterization of a Dodecameric CD 4-Ig Fusion Protein IMPLICATIONS FOR THERAPEUTIC AND VACCINE

T. Chun, A. Fauci, C. Cicala, 2002 .

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.

L. Kunkel, S. Selig, M. Anderson, 1994, Proceedings of the National Academy of Sciences of the United States of America.

(CA) repeat polymorphism in the chromosome 18 encoded dystrophin-like protein.

L. Kunkel, G. Bruns, E. Engle, 1994, Human molecular genetics.

Comparative Analysis of the APOL1 Variants in the Genetic Landscape of Renal Carcinoma Cells

K. Skorecki, E. Gottlieb, M. Tzukerman, 2022, Cancers.

The role of the CD4 receptor versus HIV coreceptors in envelope-mediated apoptosis in peripheral blood mononuclear cells.

Andrew A. White, A. Fauci, R. Rabin, 2002, Virology.

R5 and X4 HIV envelopes induce distinct gene expression profiles in primary peripheral blood mononuclear cells.

R. Lempicki, Jun Yang, T. Chun, 2006, Proceedings of the National Academy of Sciences of the United States of America.