Lista de obras - Lindsay S - Dominio Público Uruguay

3 dimensional modelling of early human brain development using optical projection tomography

artículo científico publicado en 2004

3D modelling, gene expression mapping and post-mapping image analysis in the developing human brain.

artículo científico publicado en 2005

A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid.

artículo científico publicado en 2007

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

artículo científico publicado en 2004

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

artículo científico publicado en 1998

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

artículo científico publicado en 2002

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain

artículo científico publicado en 1998

A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28

artículo científico publicado en 1994

Abnormal retinal development associated with FRMD7 mutations.

artículo científico publicado en 2014

An integrated transcriptional analysis of the developing human retina

artículo científico publicado en 2019

Anatomical and gene expression mapping of the ventral pallium in a three-dimensional model of developing human brain.

artículo científico publicado en 2005

Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.

artículo científico publicado en 2001

Charting the protomap of the human telencephalon

artículo científico publicado en 2017

Corrigendum: Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex

artículo científico publicado en 2019

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

artículo científico publicado en 2002

Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22.

artículo científico publicado en 1995

Decoding human fetal liver haematopoiesis

scientific article published on 09 October 2019

Differences in methylation on the active and inactive human X chromosomes

artículo científico publicado en 1985

Dinucleotide repeat polymorphism at the DXS559 locus

artículo científico publicado el 1 de diciembre de 1992

Dinucleotide repeat polymorphism at the DXS573 locus.

artículo científico publicado en 1993

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa ⬇️

artículo científico publicado en 2018

Distinct cortical and sub-cortical neurogenic domains for GABAergic interneuron precursor transcription factors NKX2.1, OLIG2 and COUP-TFII in early fetal human telencephalon.

artículo científico publicado en 2016

Enabling research with human embryonic and fetal tissue resources.

artículo científico publicado en 2015

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy ⬇️

artículo científico publicado el 9 de septiembre de 2010

Extracellular matrix component expression in human pluripotent stem cell-derived retinal organoids recapitulates retinogenesis in vivo and reveals an important role for IMPG1 and CD44 in the development of photoreceptors and interphotoreceptor matri

artículo científico publicado en 2018

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp

scientific article published on 01 January 1995

From spatial-data to 3D models of the developing human brain.

artículo científico publicado en 2009

Gene expression across mammalian organ development

scientific article published on 26 June 2019

Genetic and physical mapping around the properdin P gene

artículo científico publicado en 1991

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22

artículo científico publicado en 1995

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

artículo científico publicado en 1993

Glypican 3 and glypican 4 are juxtaposed in Xq26.1

artículo científico publicado en 1998

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

artículo científico publicado en 2016

Hepatic differentiation of murine embryonic stem cells

artículo científico publicado en 2002

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome

artículo científico publicado en 2008

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

artículo científico publicado en 2000

Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome

artículo científico publicado en 2012

Investigating gradients of gene expression involved in early human cortical development.

artículo científico publicado en 2010

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

artículo científico publicado en 1996

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome

scientific article published on 01 July 1993

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung

artículo científico publicado en 1998

JAtlasView: a Java atlas-viewer for browsing biomedical 3D images and atlases

artículo científico publicado en 2005

Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation.

artículo científico publicado en 2018

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

artículo científico publicado en 1997

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp

scientific article published on 01 January 1992

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

artículo científico publicado en 1990

MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression.

artículo científico publicado en 2005

Mapping human development at single-cell resolution.

artículo científico publicado en 2018

Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex.

artículo científico publicado en 2016

Neurodevelopmental protein Musashi 1 interacts with the Zika genome and promotes viral replication ⬇️

artículo científico publicado en 2017

Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization

artículo científico publicado en 1999

SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

artículo científico publicado en 2000

Spatiotemporal immune zonation of the human kidney

artículo científico publicado en 2019

Subplate in the developing cortex of mouse and human

scientific article published on 18 August 2010

The HUDSEN Atlas: a three-dimensional (3D) spatial framework for studying gene expression in the developing human brain.

artículo científico publicado en 2010

The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon

artículo científico publicado en 2017

The corticofugal neuron-associated genes ROBO1, SRGAP1, and CTIP2 exhibit an anterior to posterior gradient of expression in early fetal human neocortex development.

artículo científico publicado en 2010

The early fetal development of human neocortical GABAergic interneurons

artículo científico publicado en 2013

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

artículo científico publicado en 1992

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development

scientific journal article

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

artículo científico publicado en 2000

The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain

artículo científico publicado en 2013

Til 1--a human lymphoblastoid cell line with minimal DNA methylation

artículo científico publicado en 1989

Two dinucleotide repeat polymorphisms at the DXS571 locus

artículo científico publicado el 1 de diciembre de 1992

Ultrahigh thermal conductivity confirmed in boron arsenide

artículo científico publicado en 2018

X chromosome linkage studies in familial Rett syndrome

scientific article published on 01 January 1993

Lista de obras de Lindsay S

3 dimensional modelling of early human brain development using optical projection tomography

3D modelling, gene expression mapping and post-mapping image analysis in the developing human brain.

A comparative proteomic analysis of human and rat embryonic cerebrospinal fluid.

A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain

A study of X chromosome activity in two incontinentia pigmenti families with probable linkage to Xq28

Abnormal retinal development associated with FRMD7 mutations.

An integrated transcriptional analysis of the developing human retina

Anatomical and gene expression mapping of the ventral pallium in a three-dimensional model of developing human brain.

Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: role of Wnt3 in enhancing haematopoietic differentiation.

Charting the protomap of the human telencephalon

Corrigendum: Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex

Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPX patients.

Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22.

Decoding human fetal liver haematopoiesis

Differences in methylation on the active and inactive human X chromosomes

Dinucleotide repeat polymorphism at the DXS559 locus

Dinucleotide repeat polymorphism at the DXS573 locus.

Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa ⬇️

Distinct cortical and sub-cortical neurogenic domains for GABAergic interneuron precursor transcription factors NKX2.1, OLIG2 and COUP-TFII in early fetal human telencephalon.

Enabling research with human embryonic and fetal tissue resources.

Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy ⬇️

Extracellular matrix component expression in human pluripotent stem cell-derived retinal organoids recapitulates retinogenesis in vivo and reveals an important role for IMPG1 and CD44 in the development of photoreceptors and interphotoreceptor matri

FISH mapping of 22 novel X chromosome cosmids and the isolation of a novel microsatellite on proximal Xp

From spatial-data to 3D models of the developing human brain.

Gene expression across mammalian organ development

Genetic and physical mapping around the properdin P gene

Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22

Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.

Glypican 3 and glypican 4 are juxtaposed in Xq26.1

HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development

Hepatic differentiation of murine embryonic stem cells

Human CHN1 mutations hyperactivate alpha2-chimaerin and cause Duane's retraction syndrome

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome

Investigating gradients of gene expression involved in early human cortical development.

Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24.

Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome

Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung

JAtlasView: a Java atlas-viewer for browsing biomedical 3D images and atlases

Laminin γ3 plays an important role in retinal lamination, photoreceptor organisation and ganglion cell differentiation.

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp

Localization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosa

MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression.

Mapping human development at single-cell resolution.

Neurexins 1-3 Each Have a Distinct Pattern of Expression in the Early Developing Human Cerebral Cortex.

Neurodevelopmental protein Musashi 1 interacts with the Zika genome and promotes viral replication ⬇️

Partial cloning and assignment of WNT6 to human chromosome band 2q35 by in situ hybridization

SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development

Spatiotemporal immune zonation of the human kidney

Subplate in the developing cortex of mouse and human

The HUDSEN Atlas: a three-dimensional (3D) spatial framework for studying gene expression in the developing human brain.

The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon

The corticofugal neuron-associated genes ROBO1, SRGAP1, and CTIP2 exhibit an anterior to posterior gradient of expression in early fetal human neocortex development.

The early fetal development of human neocortical GABAergic interneurons

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

The tissue-specific RNA binding protein T-STAR controls regional splicing patterns of neurexin pre-mRNAs in the brain

Til 1--a human lymphoblastoid cell line with minimal DNA methylation

Two dinucleotide repeat polymorphisms at the DXS571 locus

Ultrahigh thermal conductivity confirmed in boron arsenide

X chromosome linkage studies in familial Rett syndrome