User profiles for Stephen J. Tapscott

Stephen J Tapscott

Fred Hutchinson Cancer Research Center
Verified email at fhcrc.org
Cited by 35591

Activation of muscle-specific genes in pigment, nerve, fat, liver, and fibroblast cell lines by forced expression of MyoD.

H Weintraub, SJ Tapscott, RL Davis… - Proceedings of the …, 1989 - National Acad Sciences
MyoD is a master regulatory gene for myogenesis. Under the control of a retroviral long
terminal repeat, MyoD was expressed in a variety of differentiated cell types by using either a …

MyoD1: a nuclear phosphoprotein requiring a Myc homology region to convert fibroblasts to myoblasts

SJ Tapscott, RL Davis, MJ Thayer, PF Cheng… - Science, 1988 - science.org
Expression of a complementary DNA (cDNA) encoding the mouse MyoD1 protein in a variety
of fibroblast and adipoblast cell lines converts them to myogenic cells. Polyclonal antisera …

MyoD and the transcriptional control of myogenesis

CA Berkes, SJ Tapscott - Seminars in cell & developmental biology, 2005 - Elsevier
The basic helix-loop-helix myogenic regulatory factors MyoD, Myf5, myogenin and MRF4
have critical roles in skeletal muscle development. Together with the Mef2 proteins and E …

Decreased expression of striatal signaling genes in a mouse model of Huntington's disease

…, CA Ross, DR Borchelt, SJ Tapscott… - Human molecular …, 2000 - academic.oup.com
To understand gene expression changes mediated by a polyglutamine repeat expansion in
the human huntingtin protein, we used oligonucleotide DNA arrays to profile ~6000 striatal …

The circuitry of a master switch: Myod and the regulation of skeletal muscle gene transcription

SJ Tapscott - 2005 - journals.biologists.com
The expression of Myod is sufficient to convert a fibroblast to a skeletal muscle cell, and, as
such, is a model system in developmental biology for studying how a single initiating event …

A unifying genetic model for facioscapulohumeral muscular dystrophy

…, GW Padberg, DG Miller, SJ Tapscott… - Science, 2010 - science.org
Facioscapulohumeral muscular dystrophy (FSHD) is a common form of muscular dystrophy
in adults that is foremost characterized by progressive wasting of muscles in the upper body. …

Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

…, GN Filippova, B Bakker, MJ Bamshad, SJ Tapscott… - Nature …, 2012 - nature.com
Facioscapulohumeral dystrophy (FSHD) is characterized by chromatin relaxation of the D4Z4
macrosatellite array on chromosome 4 and expression of the D4Z4-encoded DUX4 gene …

Conserved roles of mouse DUX and human DUX4 in activating cleavage-stage genes and MERVL/HERVL retrotransposons

…, AL Wilcox, DA Nix, CM Peterson, SJ Tapscott… - Nature …, 2017 - nature.com
To better understand transcriptional regulation during human oogenesis and preimplantation
development, we defined stage-specific transcription, which highlighted the cleavage …

Generation of neurons by transient expression of neural bHLH proteins in mammalian cells

…, JM Olson, HB Sucic, RI Hume, SJ Tapscott… - …, 2000 - journals.biologists.com
Basic helix-loop-helix (bHLH) transcription factors are known to function during mammalian
neurogenesis. Here we show that transient transfection of vectors expressing neuroD2, …

[PDF][PDF] Genome-wide MyoD binding in skeletal muscle cells: a potential for broad cellular reprogramming

…, MT Morgan, WL Ruzzo, RC Gentleman, SJ Tapscott - Developmental cell, 2010 - cell.com
Recent studies have demonstrated that MyoD initiates a feed-forward regulation of skeletal
muscle gene expression, predicting that MyoD binds directly to many genes expressed …