Lista de obras - Margrit Urbanek - Dominio Público Uruguay

A retrospective, cross-sectional study reveals that women with CRSwNP have more severe disease than men.

artículo científico publicado en 2015

A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes.

artículo científico

Accumulation of cadmium in insulin-producing β cells

artículo científico publicado en 2012

Allelic variants of the follistatin gene in polycystic ovary syndrome

artículo científico publicado en 2000

Association of fibrillin-3 and transcription factor-7-like 2 gene variants with metabolic phenotypes in PCOS.

artículo científico publicado en 2012

Associations of serum sex hormone binding globulin (SHBG) levels with SHBG gene polymorphisms in the CARDIA Male Hormone Study

scientific article published on 04 December 2007

Candidate gene region for polycystic ovary syndrome on chromosome 19p13.2.

artículo científico publicado en 2005

Characterization of a human cDNA encoding a widely expressed and highly conserved cysteine-rich protein with an unusual zinc-finger motif

artículo científico publicado en 1990

Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat

artículo científico publicado en 2011

Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.

artículo científico publicado en 2009

Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry

artículo científico publicado en 2012

Evidence for genetic linkage to alcohol dependence on chromosomes 4 and 11 from an autosome-wide scan in an American Indian population.

artículo científico publicado en 1998

Expression of a human growth hormone (hGH) receptor isoform is predicted by tissue-specific alternative splicing of exon 3 of the hGH receptor gene transcript

artículo científico publicado el 1 de febrero de 1992

FTO and MC4R gene variants are associated with obesity in polycystic ovary syndrome

artículo científico publicado en 2011

Family-Based Analysis of Candidate Genes for Polycystic Ovary Syndrome

artículo científico publicado en 2010

Family-based analysis of candidate genes for polycystic ovary syndrome

artículo científico publicado en 2010

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

artículo científico publicado en 2000

Fine mapping of genetic susceptibility to polycystic ovary syndrome on chromosome 19p13.2 and tests for regulatory activity

artículo científico publicado en 2006

First assessment of menstrual cycle function and reproductive endocrine status in Samoan women

artículo científico publicado en 2011

Gender and neurogenin3 influence the pathogenesis of ketosis-prone diabetes

artículo científico publicado en 2007

Genetic risk score for prediction of newborn adiposity and large-for-gestational-age birth

artículo científico publicado en 2014

Genetics of the polycystic ovary syndrome

artículo científico publicado en 2012

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

artículo científico publicado en 2015

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

artículo científico publicado en 2010

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

artículo científico publicado en 2013

Identification of a polycystic ovary syndrome susceptibility variant in fibrillin-3 and association with a metabolic phenotype

artículo científico publicado en 2007

Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13

artículo científico publicado en 2000

Maternal testosterone levels are associated with C-peptide levels in the Mexican American subset of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study cohort

artículo científico publicado en 2013

Parent-of-origin effects on glucose homeostasis in polycystic ovary syndrome. ⬇️

artículo científico publicado en 2014

Pathogenic Anti-Müllerian Hormone Variants in Polycystic Ovary Syndrome

artículo científico publicado en 2017

Persistence pays off for PCOS gene prospectors

artículo científico publicado en 2012

Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3

article

Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts

artículo científico publicado en 2011

Self-selected women with polycystic ovary syndrome are reproductively and metabolically abnormal and undertreated

artículo científico publicado en 2002

The apportionment of dinucleotide repeat diversity in Native Americans and Europeans: a new approach to measuring gene identity reveals asymmetric patterns of divergence.

artículo científico publicado en 1996

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

artículo científico publicado en 2013

The genetics of the polycystic ovary syndrome

artículo científico publicado en 2007

The inflammatory gene pathway is not a major contributor to polycystic ovary snydrome

artículo científico publicado en 2014

The molecular phenotype of polycystic ovary syndrome (PCOS) theca cells and new candidate PCOS genes defined by microarray analysis

artículo científico publicado en 2003

The role of TGF-β in polycystic ovary syndrome

artículo científico

The role of genetic variation in the lamin a/c gene in the etiology of polycystic ovary syndrome

artículo científico publicado en 2009

The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy

artículo científico publicado en 2012

The role of the polycystic ovary syndrome susceptibility locus D19S884 allele 8 in maternal glycemia and fetal size

artículo científico publicado en 2010

Thirty-seven candidate genes for polycystic ovary syndrome: strongest evidence for linkage is with follistatin

artículo científico publicado en 1999

Type 2 diabetes susceptibility single-nucleotide polymorphisms are not associated with polycystic ovary syndrome

artículo científico publicado en 2011

Variation in resistin gene promoter not associated with polycystic ovary syndrome

artículo científico publicado en 2003

Lista de obras de Margrit Urbanek

A retrospective, cross-sectional study reveals that women with CRSwNP have more severe disease than men.

A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes.

Accumulation of cadmium in insulin-producing β cells

Allelic variants of the follistatin gene in polycystic ovary syndrome

Association of fibrillin-3 and transcription factor-7-like 2 gene variants with metabolic phenotypes in PCOS.

Associations of serum sex hormone binding globulin (SHBG) levels with SHBG gene polymorphisms in the CARDIA Male Hormone Study

Candidate gene region for polycystic ovary syndrome on chromosome 19p13.2.

Characterization of a human cDNA encoding a widely expressed and highly conserved cysteine-rich protein with an unusual zinc-finger motif

Ethnic variation in allele distribution of the androgen receptor (AR) (CAG)n repeat

Evidence for association between polycystic ovary syndrome (PCOS) and TCF7L2 and glucose intolerance in women with PCOS and TCF7L2.

Evidence for chromosome 2p16.3 polycystic ovary syndrome susceptibility locus in affected women of European ancestry

Evidence for genetic linkage to alcohol dependence on chromosomes 4 and 11 from an autosome-wide scan in an American Indian population.

Expression of a human growth hormone (hGH) receptor isoform is predicted by tissue-specific alternative splicing of exon 3 of the hGH receptor gene transcript

FTO and MC4R gene variants are associated with obesity in polycystic ovary syndrome

Family-Based Analysis of Candidate Genes for Polycystic Ovary Syndrome

Family-based analysis of candidate genes for polycystic ovary syndrome

Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

Fine mapping of genetic susceptibility to polycystic ovary syndrome on chromosome 19p13.2 and tests for regulatory activity

First assessment of menstrual cycle function and reproductive endocrine status in Samoan women

Gender and neurogenin3 influence the pathogenesis of ketosis-prone diabetes

Genetic risk score for prediction of newborn adiposity and large-for-gestational-age birth

Genetics of the polycystic ovary syndrome

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies

Identification of a polycystic ovary syndrome susceptibility variant in fibrillin-3 and association with a metabolic phenotype

Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13

Maternal testosterone levels are associated with C-peptide levels in the Mexican American subset of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study cohort

Parent-of-origin effects on glucose homeostasis in polycystic ovary syndrome. ⬇️

Pathogenic Anti-Müllerian Hormone Variants in Polycystic Ovary Syndrome

Persistence pays off for PCOS gene prospectors

Polymorphism and genetic mapping of the human oxytocin receptor gene on chromosome 3

Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts

Self-selected women with polycystic ovary syndrome are reproductively and metabolically abnormal and undertreated

The apportionment of dinucleotide repeat diversity in Native Americans and Europeans: a new approach to measuring gene identity reveals asymmetric patterns of divergence.

The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study

The genetics of the polycystic ovary syndrome

The inflammatory gene pathway is not a major contributor to polycystic ovary snydrome

The molecular phenotype of polycystic ovary syndrome (PCOS) theca cells and new candidate PCOS genes defined by microarray analysis

The role of TGF-β in polycystic ovary syndrome

The role of genetic variation in the lamin a/c gene in the etiology of polycystic ovary syndrome

The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy

The role of the polycystic ovary syndrome susceptibility locus D19S884 allele 8 in maternal glycemia and fetal size

Thirty-seven candidate genes for polycystic ovary syndrome: strongest evidence for linkage is with follistatin

Type 2 diabetes susceptibility single-nucleotide polymorphisms are not associated with polycystic ovary syndrome

Variation in resistin gene promoter not associated with polycystic ovary syndrome