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Molecular Biology

D-Index
68
Citations
20887
World Ranking
1500
National Ranking
761

Overview

Stephen Dalton is affiliated with the University of Georgia in the United States. Their research predominantly lies within the field of Biochemistry, Genetics and Molecular Biology, with a strong focus on subfields such as Molecular Biology, Physiology, Plant Science, Surgery, and Cancer Research.

The scientist's work spans several key research topics, including:

  • Genomics and Chromatin Dynamics
  • Epigenetics and DNA Methylation
  • Pluripotent Stem Cells Research
  • Adipose Tissue and Metabolism
  • Glycosylation and Glycoproteins Research
  • RNA modifications and cancer
  • RNA and protein synthesis mechanisms

Stephen Dalton has published in a variety of notable scientific journals. Frequent publication venues include:

  • Nature
  • Nature Communications
  • Science
  • Cell Stem Cell
  • Seminars in Cell and Developmental Biology

Some of the recent papers authored or co-authored by Dalton are:

  • Expanded encyclopaedias of DNA elements in the human and mouse genomes, 2020, Nature
  • Landscape of cohesin-mediated chromatin loops in the human genome, 2020, Nature
  • Perspectives on ENCODE, 2020, Nature
  • Replication timing maintains the global epigenetic state in human cells, 2021, Science
  • Human beige adipocytes for drug discovery and cell therapy in metabolic diseases, 2020, Nature Communications

Throughout their career, Stephen Dalton has collaborated frequently with several researchers, including:

  • Michael Kulik
  • Reyes Acosta
  • Nicholas J. Addleman
  • Veena Afzal
  • Bronwen Aken

Best Publications

  • Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells.

    Karim Si‐Tayeb;Fallon K. Noto;Masato Nagaoka;Jixuan Li

  • Architectural Protein Subclasses Shape 3D Organization of Genomes during Lineage Commitment

    Jennifer E. Phillips-Cremins;Michael E G Sauria;Amartya Sanyal;Tatiana I. Gerasimova

  • Transforming growth factor alpha: mutation of aspartic acid 47 and leucine 48 results in different biological activities.

    E Lazar;S Watanabe;S Dalton;M B Sporn

  • LIF/STAT3 controls ES cell self-renewal and pluripotency by a Myc-dependent mechanism.

    Peter Cartwright;Cameron McLean;Allan Sheppard;Duane Rivett

  • Characterization of SAP-1, a Protein Recruited by Serum Response Factor to the C-Fos Serum Response Element

    Stephen Dalton;Richard Treisman

  • Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types

    Tyrone Ryba;Ichiro Hiratani;Junjie Lu;Mari Itoh

  • Transcriptional activation by the human c-Myc oncoprotein in yeast requires interaction with Max.

    Bruno Amati;Stephen Dalton;Mary W. Brooks;Trevor D. Littlewood

  • Activin A Efficiently Specifies Definitive Endoderm from Human Embryonic Stem Cells Only When Phosphatidylinositol 3‐Kinase Signaling Is Suppressed

    Amanda B McLean;Kevin A D'Amour;Karen Louise Jones;Malini Krishnamoorthy

  • Preserving the genetic integrity of human embryonic stem cells.

    Maisam M Mitalipova;Raja R Rao;Deborah M Hoyer;Julie A Johnson

  • Cell cycle regulation of the human cdc2 gene.

    Dalton S

  • Functional analysis of a growth factor-responsive transcription factor complex

    Caroline S. Hill;Richard Marais;Susan John;Judy Wynne

  • Pluripotent cell division cycles are driven by ectopic Cdk2, cyclin A/E and E2F activities.

    Elaine Stead;Josephine White;Renate Faast;Simon Conn

  • Signaling Network Crosstalk in Human Pluripotent Cells: A Smad2/3-Regulated Switch that Controls the Balance between Self-Renewal and Differentiation

    Amar M. Singh;David Reynolds;Timothy Cliff;Satoshi Ohtsuka

  • Cell cycle control of embryonic stem cells

    Josephine White;Stephen Dalton

  • Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis

    Ichiro Hiratani;Tyrone Ryba;Mari Itoh;Joy Rathjen

  • Linking the Cell Cycle to Cell Fate Decisions

    Stephen Dalton

  • The cell cycle and Myc intersect with mechanisms that regulate pluripotency and reprogramming.

    Amar M. Singh;Stephen Dalton

  • Wnt signaling and a Smad pathway blockade direct the differentiation of human pluripotent stem cells to multipotent neural crest cells

    Laura Menendez;Tatiana A. Yatskievych;Parker B. Antin;Stephen Dalton

  • Metabolic Reprogramming of Stem Cell Epigenetics

    James G. Ryall;Tim Cliff;Stephen Dalton;Vittorio Sartorelli

  • Forkhead transcription factors, Fkh1p and Fkh2p, collaborate with Mcm1p to control transcription required for M-phase

    Raman Kumar;David M Reynolds;Andrej Shevchenko;Anna Shevchenko

Frequent Co-Authors

Kelley W. Moremen
Kelley W. Moremen University of Georgia
David M. Gilbert
David M. Gilbert Florida State University
Lance Wells
Lance Wells University of Georgia
Ron Orlando
Ron Orlando University of Georgia
Jeanne F. Loring
Jeanne F. Loring Scripps Research Institute
Richard Treisman
Richard Treisman The Francis Crick Institute
Hang Yin
Hang Yin Tsinghua University
Robert J. Linhardt
Robert J. Linhardt Rensselaer Polytechnic Institute
Victor G. Corces
Victor G. Corces Emory University
Job Dekker
Job Dekker University of Massachusetts Chan Medical School

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