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Helen Stewart
Helen Stewart
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Dirección de correo verificada de bsms.ac.uk
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Large-scale discovery of novel genetic causes of developmental disorders
TW Fitzgerald, SS Gerety, WD Jones, M Van Kogelenberg, DA King, ...
Nature 519 (7542), 223, 2015
5382015
A transgenic rat model of Charcot-Marie-Tooth disease
M Sereda, I Griffiths, A Pühlhofer, H Stewart, MJ Rossner, F Zimmermann, ...
Neuron 16 (5), 1049-1060, 1996
3981996
Three markers of adult non-myelin-forming Schwann cells, 217c (Ran-1), A5E3 and GFAP: development and regulation by neuron-Schwann cell interactions
KR Jessen, L Morgan, HJ Stewart, R Mirsky
Development 109 (1), 91-103, 1990
3321990
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss
MA Simpson, MD Irving, E Asilmaz, MJ Gray, D Dafou, FV Elmslie, ...
Nature genetics 43 (4), 303-305, 2011
3162011
GAP-43 is expressed by nonmyelin-forming Schwann cells of the peripheral nervous system.
R Curtis, HJ Stewart, SM Hall, GP Wilkin, R Mirsky, KR Jessen
The Journal of cell biology 116 (6), 1455-1464, 1992
2391992
GTF2IRD1 in craniofacial development of humans and mice
M Tassabehji, P Hammond, A Karmiloff-Smith, P Thompson, ...
Science 310 (5751), 1184-1187, 2005
2352005
Galectin‐1 induces skeletal muscle differentiation in human fetal mesenchymal stem cells and increases muscle regeneration
J Chan, K O'Donoghue, M Gavina, Y Torrente, N Kennea, H Mehmet, ...
Stem cells 24 (8), 1879-1891, 2006
1712006
C offin–S iris Syndrome and the BAF Complex: Genotype–Phenotype Study in 63 Patients
GWE Santen, E Aten, AT Vulto‐van Silfhout, C Pottinger, BWM van Bon, ...
Human mutation 34 (11), 1519-1528, 2013
1662013
Identification of circulating microRNAs as diagnostic biomarkers for use in multiple myeloma
CI Jones, MV Zabolotskaya, AJ King, HJS Stewart, GA Horne, ...
British journal of cancer 107 (12), 1987-1996, 2012
1532012
Interaction between cAMP elevation, identified growth factors, and serum components in regulating Schwann cell growth
HJS Stewart, PA Eccleston, KR Jessen, R Mirsky
Journal of neuroscience research 30 (2), 346-352, 1991
1121991
Regulation of Rat Schwann Cell Po Expression and DNA Synthesis by Insulin‐like Growth Factors In Vitro
HJS Stewart, F Bradke, A Tabernero, D Morrell, KR Jessen, R Mirsky
European Journal of Neuroscience 8 (3), 553-564, 1996
1111996
Changes in DNA Synthesis Rate in the Schwann Cell Lineage In Vivo Are Correlated With the Precursor – Schwann Cell Transition and Myelination
HJS Stewart, L Morgan, KR Jessen, R Mirsky
European Journal of Neuroscience 5 (9), 1136-1144, 1993
1081993
GAP-43 immunoreactivity is widespread in the autonomic neurons and sensory neurons of the rat
HJS Stewart, T Cowen, R Curtis, GP Wilkin, R Mirsky, KR Jessen
Neuroscience 47 (3), 673-684, 1992
1001992
BRD 4 associates with p53 in DNMT 3A‐mutated leukemia cells and is implicated in apoptosis by the bromodomain inhibitor JQ 1
HJS Stewart, GA Horne, S Bastow, TJT Chevassut
Cancer medicine 2 (6), 826-835, 2013
902013
Lack of galectin‐1 results in defects in myoblast fusion and muscle regeneration
V Georgiadis, HJS Stewart, HJ Pollard, Y Tavsanoglu, R Prasad, ...
Developmental dynamics: an official publication of the American Association …, 2007
902007
TGF‐βs upregulate NCAM and L1 expression in cultured Schwann cells, suppress cyclic AMP–induced expression of O4 and galactocerebroside, and are widely expressed in cells of …
HJS Stewart, G Rougon, Z Dong, C Dean, KR Jessen, R Mirsky
Glia 15 (4), 419-436, 1995
861995
Expression of c‐Jun, Jun B, Jun D and cAMP Response Element Binding Protein by Schwann Cells and their Precursors In Vivo and In Vitro
HJS Stewart
European Journal of Neuroscience 7 (6), 1366-1375, 1995
731995
Expression and regulation of α1β1 integrin in Schwann cells
HJS Stewart, D Turner, KR Jessen, R Mirsky
Journal of neurobiology 33 (7), 914-928, 1997
721997
Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene
J Uusimaa, J Evans, C Smith, A Butterworth, K Craig, N Ashley, C Liao, ...
European Journal of Human Genetics 22 (2), 184-191, 2014
702014
A large-scale mutation search reveals genetic heterogeneity in 3M syndrome
C Huber, AL Delezoide, F Guimiot, C Baumann, V Malan, M Le Merrer, ...
European journal of human genetics 17 (3), 395-400, 2009
652009
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