M. Fisher

发表

Visualization of Gene Expression and Expression as a Phenotype with the XPO, XAO and DO using a Combination of Experimental Data Sources

Ying Wang, Troy J. Pells, Malcolm E. Fisher, 2018, ICBO.

Navigating Xenbase: An Integrated Xenopus Genomics and Gene Expression Database.

Troy J. Pells, Kevin A. Burns, K. Karimi, 2018, Methods in molecular biology.

Transcribed enhancers lead waves of coordinated transcription in transitioning mammalian cells

Thomas J. Ha, Kelly J. Morris, Louise N. Winteringham, 2015, Science.

Edinburgh Research Explorer Endogenous Retrotransposition Activates Oncogenic Pathways in Hepatocellular Carcinoma Endogenous Retrotransposition Activates Oncogenic Pathways in Hepatocellular Carcinoma

Piero Carninci, G. Natoli, G. Faulkner, 2022 .

FANTOM5 CAGE profiles of human and mouse samples

Jay W. Shin, Thomas J. Ha, Kelly J. Morris, 2017, Scientific Data.

Comparative Analysis of 3D Expression Patterns of Transcription Factor Genes and Digit Fate Maps in the Developing Chick Wing

C. Tickle, M. Fisher, A. Sherman, 2011, PloS one.

Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla

R. Evans, W. Alaynick, M. Fisher, 2010, Human molecular genetics.

UvA-DARE ( Digital Academic Repository ) Loss of the BMP Antagonist , SMOC-1 , Causes Ophthalmo-Acromelic ( Waardenburg Anophthalmia ) Syndrome in Humans and Mice

Wieczorek, Dagmar, Rosanna, 2011 .

3D expression patterns of cell cycle genes in the developing chick wing and comparison with expression patterns of genes implicated digit

M. Fisher, Gordana Pavlovska, F. Bangs, 2011 .

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Fitzpatrick, 2013, PLoS genetics.

Xenbase: Facilitating the Use of Xenopus to Model Human Disease

Troy J. Pells, Kevin A. Burns, K. Karimi, 2019, Front. Physiol..

Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

I. Jackson, R. Hennekam, H. Brunner, 2011, PLoS genetics.

Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence

A. Munnich, H. R. Crollius, D. McBride, 2009, Nature Genetics.

A promoter-level mammalian expression atlas

Cesare Furlanello, Finn Drabløs, Carsten O. Daub, 2015 .

3D expression patterns of cell cycle genes in the developing chick wing and comparison with expression patterns of genes implicated in digit specification

C. Tickle, M. Fisher, M. Welten, 2011, Developmental dynamics : an official publication of the American Association of Anatomists.

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

W. Reardon, M. Simpson, R. Trembath, 2011, American journal of human genetics.

eFGF is required for activation of XmyoD expression in the myogenic cell lineage of Xenopus laevis.

M. Fisher, M. Pownall, H. Isaacs, 2002, Development.

Xenbase: a genomic, epigenomic and transcriptomic model organism database

Ying Wang, Troy J. Pells, Malcolm E. Fisher, 2017, Nucleic Acids Res..

Cloning and characterisation of Myf5 and MyoD orthologues in Xenopus tropicalis

M. Fisher, M. Pownall, P. Branney, 2003, Biology of the cell.

EMAGE mouse embryo spatial gene expression database: 2010 update

Nicholas Burton, Richard A. Baldock, Yiya Yang, 2009, Nucleic Acids Res..

Xenbase: deep integration of GEO & SRA RNA-seq and ChIP-seq data in a model organism database

Troy J. Pells, Kevin A. Burns, K. Karimi, 2019, Nucleic Acids Res..

Identification of genes downstream of the Shh signalling in the developing chick wing and syn-expressed with Hoxd13 using microarray and 3D computational analysis

C. Tickle, R. Baldock, D. Burt, 2010, Mechanisms of Development.

Explorer Integrating technologies for comparing 3 D gene expression domains in the developing chick limb

C. Tickle, R. Baldock, D. Davidson, 2017 .

Integrating technologies for comparing 3D gene expression domains in the developing chick limb

Paula Murphy, Malcolm E. Fisher, Cheryll Tickle, 2008, Developmental biology.

The Xenopus phenotype ontology: bridging model organism phenotype data to human health and development

Troy J. Pells, Bradley I. Arshinoff, K. Karimi, 2021, bioRxiv.

Disruption of ST5 is associated with mental retardation and multiple congenital anomalies

M. Vikkula, A. Winterpacht, M. Fisher, 2009, Journal of Medical Genetics.

Disruption of ST 5 is associated with mental retardation and multiple congenital anomalies

M. Vikkula, A. Winterpacht, M. Fisher, 2010 .

The Gene Ontology knowledgebase in 2023

Silvio C. E. Tosatto, Steven J. Marygold, Suzi A Aleksander, 2023, Genetics.

Xenbase: key features and resources of the Xenopus model organism knowledgebase

Troy J. Pells, Bradley I. Arshinoff, K. Karimi, 2023, Genetics.

FANTOM5 CAGE profiles of human and mouse samples.

Jay W. Shin, Thomas J. Ha, Kelly J. Morris, 2017, Scientific data.

Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice

I. Jackson, R. Hennekam, H. Brunner, 2018, PLoS Genetics.

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Keene, 2013, PLoS genetics.

A promoter-level mammalian expression atlas

Martin S. Taylor, Jay W. Shin, Thomas J. Ha, 2014, Nature.

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

W. Reardon, M. Simpson, R. Trembath, 2011, American Journal of Human Genetics.

Integrating technologies for comparing 3D gene expression domains in the developing chick limb

C. Tickle, R. Baldock, D. Davidson, 2008, Developmental biology.