Lista de obras - David I Wilson - Dominio Público Uruguay

ADAM33 expression in asthmatic airways and human embryonic lungs

artículo científico publicado en 2005

BRCA1 EXON 11, a CERES (composite regulatory element of splicing) element involved in splice regulation

artículo científico publicado en 2014

BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.

artículo científico

Beta cell differentiation during early human pancreas development

artículo científico publicado en 2004

Beta-cell differentiation during human development does not rely on nestin-positive precursors: implications for stem cell-derived replacement therapy

artículo científico publicado en 2002

Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731

artículo científico publicado en 2010

Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration

artículo científico publicado en 2005

Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation

artículo científico publicado en 2004

Differences between human and mouse alpha-fetoprotein expression during early development

scientific article published on 01 May 2001

Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis

artículo científico publicado en 2008

Epigenetic regulation during fetal femur development: DNA methylation matters.

artículo científico publicado en 2013

Evaluating Human Embryonic Germ Cells: Concord and Conflict as Pluripotent Stem Cells

artículo científico publicado en 2006

Evidence for centriolar satellite localization of CDK1 and cyclin B2.

artículo científico publicado en 2013

Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1.

artículo científico publicado en 2013

Expression and localisation of thymosin beta-4 in the developing human early fetal heart

artículo científico publicado en 2018

Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation

artículo científico publicado en 2001

FRA2A is a CGG repeat expansion associated with silencing of AFF3

artículo científico publicado en 2014

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

artículo científico publicado en 2014

Hepatic differentiation of murine embryonic stem cells

artículo científico publicado en 2002

Human embryo and early fetus research

artículo científico publicado en 2006

Human embryonic germ cells for future neuronal replacement therapy

artículo científico publicado en 2005

Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis.

artículo científico publicado en 2016

In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development

artículo científico publicado en 2006

In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

artículo científico publicado en 2010

In vitro fertilization improves childhood growth and metabolism.

artículo científico publicado en 2007

Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy

artículo científico publicado en 2009

Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome

artículo científico publicado en 2015

MicroRNA-146a regulates human foetal femur derived skeletal stem cell differentiation by down-regulating SMAD2 and SMAD3.

artículo científico publicado en 2014

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

artículo científico publicado en 2002

Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis

artículo científico publicado en 2002

Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.

artículo científico publicado en 2012

Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia

artículo científico publicado en 2002

Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment

artículo científico publicado en 2007

Probing the epigenetic regulation of HIF-1α transcription in developing tissue.

artículo científico publicado en 2015

RBFOX2 protein domains and cellular activities.

artículo científico publicado en 2014

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

artículo científico publicado en 2014

Rare variants in NR2F2 cause congenital heart defects in humans

artículo científico publicado en 2014

Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo

artículo científico publicado en 2015

Science, medicine, and the future: Genetics and cardiovascular risk.

artículo científico publicado en 2001

Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.

artículo científico publicado en 2009

Soluble ADAM33 initiates airway remodeling to promote susceptibility for allergic asthma in early life

artículo científico publicado en 2016

Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease

artículo científico publicado en 2010

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

artículo científico publicado en 2005

The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture

artículo científico publicado en 2008

The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma

artículo científico publicado en 2008

Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

artículo científico publicado en 2010

Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.

artículo científico publicado en 2009

Lista de obras de David I Wilson

ADAM33 expression in asthmatic airways and human embryonic lungs

BRCA1 EXON 11, a CERES (composite regulatory element of splicing) element involved in splice regulation

BRCA1 exon 11 alternative splicing, multiple functions and the association with cancer.

Beta cell differentiation during early human pancreas development

Beta-cell differentiation during human development does not rely on nestin-positive precursors: implications for stem cell-derived replacement therapy

Centriolar association of ALMS1 and likely centrosomal functions of the ALMS motif-containing proteins C10orf90 and KIAA1731

Characterization and multipotentiality of human fetal femur-derived cells: implications for skeletal tissue regeneration

Characterization of ciliated bronchial epithelium 1, a ciliated cell-associated gene induced during mucociliary differentiation

Differences between human and mouse alpha-fetoprotein expression during early development

Ectopic SOX9 mediates extracellular matrix deposition characteristic of organ fibrosis

Epigenetic regulation during fetal femur development: DNA methylation matters.

Evaluating Human Embryonic Germ Cells: Concord and Conflict as Pluripotent Stem Cells

Evidence for centriolar satellite localization of CDK1 and cyclin B2.

Evidence for reciliation of RPE1 cells in late G1 phase, and ciliary localisation of cyclin B1.

Expression and localisation of thymosin beta-4 in the developing human early fetal heart

Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: potential interactions in gene regulation

FRA2A is a CGG repeat expansion associated with silencing of AFF3

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

Hepatic differentiation of murine embryonic stem cells

Human embryo and early fetus research

Human embryonic germ cells for future neuronal replacement therapy

Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis.

In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development

In vitro expression of NGN3 identifies RAB3B as the predominant Ras-associated GTP-binding protein 3 family member in human islets

In vitro fertilization improves childhood growth and metabolism.

Induction of a disintegrin and metalloprotease 33 during embryonic lung development and the influence of IL-13 or maternal allergy

Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome

MicroRNA-146a regulates human foetal femur derived skeletal stem cell differentiation by down-regulating SMAD2 and SMAD3.

Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome

Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis

Nek2 localises to the distal portion of the mother centriole/basal body and is required for timely cilium disassembly at the G2/M transition.

Novel SOX9 expression during human pancreas development correlates to abnormalities in Campomelic dysplasia

Phospholamban and sarcolipin are maintained in the endoplasmic reticulum by retrieval from the ER-Golgi intermediate compartment

Probing the epigenetic regulation of HIF-1α transcription in developing tissue.

RBFOX2 protein domains and cellular activities.

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Rare variants in NR2F2 cause congenital heart defects in humans

Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo

Science, medicine, and the future: Genetics and cardiovascular risk.

Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.

Soluble ADAM33 initiates airway remodeling to promote susceptibility for allergic asthma in early life

Stem cell marker TRA-1-60 is expressed in foetal and adult kidney and upregulated in tubulo-interstitial disease

Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes

The early human germ cell lineage does not express SOX2 during in vivo development or upon in vitro culture

The soluble form of a disintegrin and metalloprotease 33 promotes angiogenesis: implications for airway remodeling in asthma

Transcriptional regulation of the Alström syndrome gene ALMS1 by members of the RFX family and Sp1

Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings.