S. Lindsay

发表

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

R. Baldock, D. Davidson, J. Sharpe, 2005, Brain Research Bulletin.

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

G. Clowry, A. Copp, D. Gerrelli, 2016, Front. Neuroanat..

Gene expression across mammalian organ development

J. Baker, P. Khaitovich, W. Huber, 2019, Nature.

Mapping human development at single-cell resolution

S. Teichmann, S. Behjati, M. Haniffa, 2018, Development.

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

Richard Baldock, Duncan Davidson, James Sharpe, 2004, BMC Neuroscience.

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

I. Glass, T. Strachan, R. Zeller, 2000, Human molecular genetics.

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

Colin A. Johnson, J. Al-Aama, S. Mehrotra, 2018, Nature Communications.

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

Richard Baldock, Xunxian Wang, Yiya Yang, 2010, Journal of anatomy.

The Early Fetal Development of Human Neocortical GABAergic Interneurons

Gavin J. Clowry, Susan Lindsay, G. Clowry, 2013, Cerebral cortex.

Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum

P. Hof, I. Glass, D. Gerrelli, 2019, Science.

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

S. Scherer, P. Scambler, W. Reardon, 1998, Nature Genetics.

Deposited in DRO : 25 October 2018 Version of attached le : Published Version Peer-review status of attached

Colin A. Johnson, J. Al-Aama, S. Mehrotra, 2018 .

An improved method for the simultaneous demonstration of mRNA and esterase activity at the human neuromuscular junction

R. Vater, S. Lindsay, C. Young, 2004, The Histochemical Journal.

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

D. Schlessinger, J. Clayton-Smith, J. Hurst, 1997, Journal of Medical Genetics.

Abnormal retinal development associated with FRMD7 mutations

Mervyn G. Thomas, I. Gottlob, M. Crosier, 2014, Human molecular genetics.

Isolation of a full-length human WNT7A gene implicated in limb development and cell transformation, and mapping to chromosome 3p25.

M. Lako, T. Strachan, S. Lindsay, 1997, Gene.

Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination

David I. Wilson, H. Ostrer, T. Strachan, 1999, Mechanisms of Development.

A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas

A. Harris, T. Strachan, S. Ruben, 1997, Oncogene.

A novel family of cathepsin L-like (CTSLL) sequences on human chromosome 10q and related transcripts.

S. Lindsay, J. Lunec, N. Spurr, 1994, Genomics.

Truncation of NHEJ1 in a patient with polymicrogyria

N. Philip, D. Figarella-Branger, S. Lindsay, 2007, Human mutation.

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.

M. Lako, T. Strachan, S. Lindsay, 1998, Gene.

Utrophin mRNA Expression in Muscle Is Not Restricted to the Neuromuscular Junction

K. Davies, R. Vater, S. Lindsay, 1998, Molecular and Cellular Neuroscience.

Partial cloning and assignment1 of WNT6 to human chromosome band 2q35 by in situ hybridization

M. Lako, T. Strachan, S. Lindsay, 1999, Cytogenetic and Genome Research.

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

A. Collins, S. Lindsay, C. Oley, 1995, American journal of medical genetics.

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 matrix.

J. Al-Aama, N. Krasnogor, M. Lako, 2018, Acta biomaterialia.

Hepatic differentiation of murine embryonic stem cells.

David I. Wilson, S. Lindsay, D. Tosh, 2001, Experimental cell research.

The embryological basis of subclinical hypertrophic cardiomyopathy

Perry M. Elliott, Kevin Mills, Paul Bassett, 2016, Scientific Reports.

DEV122820 3073..3076

A. Copp, D. Gerrelli, S. Lindsay, 2015 .

Differences in methylation on the active and inactive human X chromosomes

A. Riggs, S. Lindsay, R. Holliday, 1985, Annals of human genetics.

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

I. Krantz, T. Strachan, S. Lindsay, 2004, Human Genetics.

Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.

T. Strachan, S. Lindsay, I. Cross, 1995, Journal of medical genetics.

An integrated transcriptional analysis of the developing human retina

Jannetta S. Steyn, Osagie G. Izuogu, S. Grellscheid, 2019, Development.

Sequence of the promoter region of the gene for human X-linked 3-phosphoglycerate kinase.

A. Riggs, D. Keith, R. Simmer, 1984, Gene.

The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development.

I. Gottlob, M. Crosier, S. Lindsay, 2010, Human molecular genetics.

Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors

Sarah A. Teichmann, Dyanne Rampling, Imran Mushtaq, 2018, Science.

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

K. Davies, I. Glass, A. Fielder, 1993, Journal of medical genetics.

WDR62 is associated with the spindle pole and is mutated in human microcephaly

C. Woods, F. Gergely, S. Lindsay, 2010, Nature Genetics.

Autosomal dominant sacral agenesis: Currarino syndrome

T. Strachan, S. Lindsay, J. Burn, 2000, Journal of medical genetics.

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

David I. Wilson, H. Ostrer, T. Strachan, 2000, Mechanisms of Development.

Gene expression across mammalian organ development

P. Khaitovich, W. Huber, I. Xenarios, 2019, Nature.

Decoding human fetal liver haematopoiesis

David McDonald, Kerstin B. Meyer, Jaume Bacardit, 2019, Nature.

Genetic and physical mapping around the properdin P gene.

H. Willard, K. Davies, A. Wright, 1991, Genomics.

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

K. Davies, I. Glass, A. Fielder, 2022 .

PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28.

T. Berney, K. Davies, S. Knight, 1996, American journal of human genetics.

Glypican 3 and glypican 4 are juxtaposed in Xq26.1.

R. Mazzarella, E. Chen, S. Lindsay, 1998, Gene.

X chromosome linkage studies in familial Rett syndrome

S. Bhattacharya, A. Clarke, S. Lindsay, 2004, Human Genetics.

Use of restriction enzymes to detect potential gene sequences in mammalian DNA

A. Bird, S. Lindsay, 1987, Nature.

Spatiotemporal immune zonation of the human kidney

Sarah A. Teichmann, Dyanne Rampling, Imran Mushtaq, 2019, Science.

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

C. Woods, F. Gergely, A. Firth, 2017, Science.

HSF access to heat shock elements in vivo de~ends criticallv on Promoter architeiture defined b; GAGA factor,

S. Lindsay, T. John, 1995 .

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

G. Clowry, S. Lindsay, Yaobo Xu, 2016, Cerebral cortex.

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

D. Schlessinger, J. Clayton-Smith, J. Hurst, 1997, Journal of medical genetics.

Decoding the development of the blood and immune systems during human fetal liver haematopoiesis

Jaume Bacardit, Sarah A. Teichmann, Berthold Göttgens, 2019, bioRxiv.

CAC--the neglected repeat.

S. Lindsay, A. Sertedaki, 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

T. Meitinger, Mohan L Gupta, D. Hunter, 2010, Cell.

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

M. Patton, T. Strachan, S. Lindsay, 2002, Human molecular genetics.

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

Susan Lindsay, A. Copp, S. Lindsay, 2005, Trends in genetics : TIG.

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

J. Beckmann, T. Strachan, S. Lindsay, 2000, Human molecular genetics.

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

C. Walsh, S. Gygi, S. Lindsay, 2007, Journal of proteome research.

The Tissue-Specific RNA Binding Protein T-STAR Controls Regional Splicing Patterns of Neurexin Pre-mRNAs in the Brain

G. Clowry, M. Crosier, S. Lindsay, 2013, PLoS genetics.

A Molecular Neuroanatomical Study of the Developing Human Neocortex from 8 to 17 Postconceptional Weeks Revealing the Early Differentiation of the Subplate and Subventricular Zone

G. Clowry, S. Lindsay, N. Bayatti, 2007, Cerebral cortex.

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

S. Lindsay, M. Monk, R. Adams, 1989, Human Genetics.

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

M. Lako, T. Strachan, S. Lindsay, 1998, Human molecular genetics.

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

M. Lako, S. Lindsay, P. Cairns, 2001, Mechanisms of Development.

Molecular Genetics of Early Human Development

David I. Wilson, T. Strachan, S. Lindsay, 1997 .

Enabling research with human embryonic and fetal tissue resources

Andrew J. Copp, Dianne Gerrelli, Susan Lindsay, 2015, Development.

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

G. Clowry, J. Kerwin, S. Lindsay, 2016, Brain Structure and Function.

Charting the protomap of the human telencephalon.

G. Clowry, Subrot Sarma, J. Kerwin, 2017, Seminars in cell & developmental biology.

Human CHN1 Mutations Hyperactivate α2-Chimaerin and Cause Duane's Retraction Syndrome

Alfonso Baldi, Michelle Cheung, Mustafa Sahin, 2008, Science.

Subplate in the developing cortex of mouse and human

Latha Srinivasan, Wei Zhi Wang, Susan Lindsay, 2010, Journal of anatomy.

A Study of X Chromosome Activity in Two Incontinentia pigmenti Families with Probable Linkage to Xq28

S. Bhattacharya, A. Clarke, S. Lindsay, 1994, European journal of human genetics : EJHG.

Investigating gradients of gene expression involved in early human cortical development

Susan Lindsay, G. Clowry, S. Lindsay, 2010, Journal of anatomy.

Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development

G. Clowry, J. Eyre, Subrot Sarma, 2008, The European journal of neuroscience.

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

G. Clowry, S. Lindsay, S. Lisgo, 2017, Cerebral cortex.

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

S. Klauck, A. Poustka, S. Lindsay, 2002, American journal of human genetics.

The Corticofugal Neuron-Associated Genes ROBO1, SRGAP1, and CTIP2 Exhibit an Anterior to Posterior Gradient of Expression in Early Fetal Human Neocortex Development

G. Clowry, S. Lindsay, N. Bayatti, 2010, Cerebral cortex.

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.

C. Woods, M. Crosier, Tanyeri Barak, 2011, American journal of human genetics.

Investigating Embryonic Expression Patterns and Evolution of AHI1 and CEP290 Genes, Implicated in Joubert Syndrome

S. Lindsay, J. Sayer, R. Simms, 2012, PloS one.

In Vitro Modelling of Cortical Neurogenesis by Sequential Induction of Human Umbilical Cord Blood Stem Cells

G. Clowry, A. Trevelyan, S. Lindsay, 2012, Stem Cell Reviews and Reports.

Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly

F. Alkuraya, S. Lindsay, S. Lisgo, 2021, Journal of Medical Genetics.

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

M. Lako, S. Lindsay, D. Steel, 2018, Cell Death & Disease.

Volume contents

Singapore., France, E. Wilder, 2001, Mechanisms of Development.

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.

Directed differentiation of umbilical cord blood stem cells into cortical GABAergic neurons.

A. Dashti, S. Lindsay, F. Al-Mulla, 2013, Acta neurobiologiae experimentalis.

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene.

P. Scambler, W. Reardon, R. Winter, 2000, American journal of human genetics.

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.

C. Woods, M. Crosier, Tanyeri Barak, 2011, American journal of human genetics.

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

D. Goudie, S. Lindsay, M. Porteous, 1992, Genomics.

J. Al-Aama, N. Krasnogor, M. Lako, 2018, Acta biomaterialia.

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

Nick Burton, Bill Hill, Richard A. Baldock, 2005, BMC Bioinformatics.

This Work Is Licensed under a Creative Commons Attribution 3.0 Unported License Date Deposited: the Early Fetal Development of Human Neocortical Gabaergic Interneurons

G. Clowry, Subrot Sarma, S. Lindsay, 2022 .

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

M. Crosier, S. Lindsay, S. Hayflick, 2010, Brain Research Bulletin.

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

F. Gergely, S. Lindsay, R. Bayliss, 2017, Science.

The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus.

Mervyn G. Thomas, R. Hertle, P. Tarpey, 2011, Brain : a journal of neurology.