Lista de obras - Anna K Naumova - Dominio Público Uruguay

A cloned unique gene of Drosophila melanogaster contains a repetitive 3' exon whose sequence is present at the 3' ends of many different mRNAs

artículo científico publicado en 1982

A longitudinal study of X-inactivation ratio in human females

scientific article published on 28 August 2004

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation ⬇️

artículo científico publicado el 1 de noviembre de 1997

A survey of genetic and epigenetic variation affecting human gene expression

artículo científico publicado en 2004

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

artículo científico publicado en 2009

Alternative splicing and imprinting control of the Meg3/Gtl2-Dlk1 locus in mouse embryos.

artículo científico publicado en 2003

Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines

artículo científico publicado en 2010

Chromosomal localization of mouse and human genes encoding the splicing factors ASF/SF2 (SFRS1) and SC-35 (SFRS2)

artículo científico publicado en 1995

Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma

artículo científico publicado en 1994

Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked

artículo científico publicado en 1997

Coordinated diurnal regulation of genes from the Dlk1-Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes

artículo científico publicado en 2007

DNA methyltransferase 1 (Dnmt1) mutation affects Snrpn imprinting in the mouse male germ line

artículo científico publicado en 2012

Dynamics of response to asynapsis and meiotic silencing in spermatocytes from Robertsonian translocation carriers

artículo científico publicado en 2013

Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

artículo científico publicado en 1998

Genomic imprinting variations in the mouse type 3 deiodinase gene between tissues and brain regions.

artículo científico publicado en 2014

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

artículo científico publicado en 2009

Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?

artículo científico publicado en 2001

Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development

scientific article published on 01 January 2002

Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines

artículo científico publicado en 2012

Long-QT syndrome

artículo científico publicado en 2007

Loss of the zona pellucida-binding protein 2 (Zpbp2) gene in mice impacts airway hypersensitivity and lung lipid metabolism in a sex-dependent fashion

artículo científico publicado en 2018

Novel imprinted transcripts from the Dlk1-Gtl2 intergenic region, Mico1 and Mico1os, show circadian oscillations

artículo científico publicado en 2008

Oocyte heterogeneity with respect to the meiotic silencing of unsynapsed X chromosomes in the XY female mouse.

artículo científico publicado en 2013

Parental effect of DNA (Cytosine-5) methyltransferase 1 on grandparental-origin-dependent transmission ratio distortion in mouse crosses and human families

artículo científico publicado en 2008

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

artículo científico publicado en 1998

Physical and meiotic mapping of the region of human chromosome 4q11-q13 encompassing the vitamin D binding protein DBP/Gc-globulin and albumin multigene cluster

artículo científico publicado en 1999

Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp.

artículo científico publicado en 1998

Preferential amplification of the paternal allele in neuroblastomas with N-myc amplification

scientific article published on 01 January 1994

Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas

artículo científico publicado en 1993

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus

artículo científico publicado en 2000

Robertsonian translocations modify genomic distribution of γH2AFX and H3.3 in mouse germ cells

artículo científico publicado en 2016

Role of DNA methylation in expression control of the IKZF3-GSDMA region in human epithelial cells

artículo científico publicado en 2017

Screening for pain phenotypes: analysis of three congenic mouse strains on a battery of nine nociceptive assays

artículo científico publicado en 2006

Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma

artículo científico publicado en 2013

The Yin and Yang of pain: variability in formalin test nociception and morphine analgesia produced by the Yin Yang 1 transcription factor gene.

artículo científico publicado en 2013

The genetics of retinoblastoma, revisited

artículo científico publicado en 1994

Transmission ratio distortion in the myotonic dystrophy locus in human preimplantation embryos

artículo científico publicado en 2006

Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation

artículo científico publicado en 1995

Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome

artículo científico publicado en 1996

Twin study of genetic and aging effects on X chromosome inactivation

artículo científico publicado en 2005

When Does the Epigenome Become "Sexy"?

scientific article published on 15 July 2018

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells.

artículo científico publicado en 2018

[DNA of the hepatitis B virus in human generative cells]

artículo científico publicado en 1986

[Detection of nucleotide sequences homologous to the DNA of the hepatitis B virus in human placental DNA]

artículo científico publicado en 1983

[Hepatitis B virus and the development of human embryonal tumors]

scientific article published on 01 January 1988

[Integration of hepatitis B virus DNA into the human neuroblastoma cell genome]

scientific article published on 01 July 1993

Interacción regulatoria entre la región ZPBP2-ORMDL3/Zpbp2-Ormdl3 y el reloj circadiano

artículo científico publicado el 27 de septiembre de 2019

Lista de obras de Anna K Naumova

A cloned unique gene of Drosophila melanogaster contains a repetitive 3' exon whose sequence is present at the 3' ends of many different mRNAs

A longitudinal study of X-inactivation ratio in human females

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation ⬇️

A survey of genetic and epigenetic variation affecting human gene expression

Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

Alternative splicing and imprinting control of the Meg3/Gtl2-Dlk1 locus in mouse embryos.

Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell lines

Chromosomal localization of mouse and human genes encoding the splicing factors ASF/SF2 (SFRS1) and SC-35 (SFRS2)

Concordance between parental origin of chromosome 13q loss and chromosome 6p duplication in sporadic retinoblastoma

Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked

Coordinated diurnal regulation of genes from the Dlk1-Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes

DNA methyltransferase 1 (Dnmt1) mutation affects Snrpn imprinting in the mouse male germ line

Dynamics of response to asynapsis and meiotic silencing in spermatocytes from Robertsonian translocation carriers

Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

Genomic imprinting variations in the mouse type 3 deiodinase gene between tissues and brain regions.

Global patterns of cis variation in human cells revealed by high-density allelic expression analysis

Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?

Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development

Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines

Long-QT syndrome

Loss of the zona pellucida-binding protein 2 (Zpbp2) gene in mice impacts airway hypersensitivity and lung lipid metabolism in a sex-dependent fashion

Novel imprinted transcripts from the Dlk1-Gtl2 intergenic region, Mico1 and Mico1os, show circadian oscillations

Oocyte heterogeneity with respect to the meiotic silencing of unsynapsed X chromosomes in the XY female mouse.

Parental effect of DNA (Cytosine-5) methyltransferase 1 on grandparental-origin-dependent transmission ratio distortion in mouse crosses and human families

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

Physical and meiotic mapping of the region of human chromosome 4q11-q13 encompassing the vitamin D binding protein DBP/Gc-globulin and albumin multigene cluster

Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of Xp.

Preferential amplification of the paternal allele in neuroblastomas with N-myc amplification

Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas

Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus

Robertsonian translocations modify genomic distribution of γH2AFX and H3.3 in mouse germ cells

Role of DNA methylation in expression control of the IKZF3-GSDMA region in human epithelial cells

Screening for pain phenotypes: analysis of three congenic mouse strains on a battery of nine nociceptive assays

Sex- and age-dependent DNA methylation at the 17q12-q21 locus associated with childhood asthma

The Yin and Yang of pain: variability in formalin test nociception and morphine analgesia produced by the Yin Yang 1 transcription factor gene.

The genetics of retinoblastoma, revisited

Transmission ratio distortion in the myotonic dystrophy locus in human preimplantation embryos

Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation

Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome

Twin study of genetic and aging effects on X chromosome inactivation

When Does the Epigenome Become "Sexy"?

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells.

[DNA of the hepatitis B virus in human generative cells]

[Detection of nucleotide sequences homologous to the DNA of the hepatitis B virus in human placental DNA]

[Hepatitis B virus and the development of human embryonal tumors]

[Integration of hepatitis B virus DNA into the human neuroblastoma cell genome]

Interacción regulatoria entre la región ZPBP2-ORMDL3/Zpbp2-Ormdl3 y el reloj circadiano