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David E Barton
David E Barton
Adjunct Associate Professor of Molecular Genetics, University College Dublin
Email verificata su ucd.ie - Home page
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Anno
Identification of a cDNA encoding a parathyroid hormone-like peptide from a human tumor associated with humoral hypercalcemia of malignancy.
M Mangin, AC Webb, BE Dreyer, JT Posillico, K Ikeda, EC Weir, ...
Proceedings of the National Academy of Sciences 85 (2), 597-601, 1988
5071988
Molecular characterization and chromosomal mapping of melanoma growth stimulatory activity, a growth factor structurally related to beta‐thromboglobulin.
A Richmond, E Balentien, HG Thomas, G Flaggs, DE Barton, J Spiess, ...
The EMBO journal 7 (7), 2025-2033, 1988
4261988
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
FJ Couch, X Wang, L McGuffog, A Lee, C Olswold, KB Kuchenbaecker, ...
PLoS genetics 9 (3), e1003212, 2013
3282013
Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility
AT Rovio, DR Marchington, S Donat, HC Schuppe, J Abel, E Fritsche, ...
Nature genetics 29 (3), 261-262, 2001
2232001
A melanocyte-specific gene, Pmel 17, maps near the silver coat color locus on mouse chromosome 10 and is in a syntenic region on human chromosome 12.
BS Kwon, C Chintamaneni, CA Kozak, NG Copeland, DJ Gilbert, ...
Proceedings of the National Academy of Sciences 88 (20), 9228-9232, 1991
2111991
Human tyrosinase gene, mapped to chromosome 11 (q14→ q21), defines second region of homology with mouse chromosome 7
DE Barton, BS Kwon, U Francke
Genomics 3 (1), 17-24, 1988
2061988
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
M Verbitsky, R Westland, A Perez, K Kiryluk, Q Liu, P Krithivasan, ...
Nature genetics 51 (1), 117-127, 2019
1902019
Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence
DC Rubinsztein, W Amos, J Leggo, S Goodburn, RS Ramesar, J Old, ...
Nature Genetics 7 (4), 525-530, 1994
1851994
A novel protein tyrosine kinase gene whose expression is modulated during endothelial-cell differentiation
M Ruta, R Howk, G Ricca, W Drohan, M Zabelshansky, G Laureys, ...
Oncogene 3 (1), 9-15, 1988
1811988
The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-binding
RA Spritz, K Strunk, CS Surowy, SO Hoch, DE Barton, U Francke
Nucleic acids research 15 (24), 10373-10391, 1987
1721987
Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased …
DC Rubinsztein, DE Barton, BC Davison, MA Ferguson-Smith
Human molecular genetics 2 (10), 1713-1715, 1993
1661993
The detection of large deletions or duplications in genomic DNA
JAL Armour, DE Barton, DJ Cockburn, GR Taylor
Human Mutation 20 (5), 325-337, 2002
1642002
Chromosomal mapping of genes for transforming growth factors beta 2 and beta 3 in man and mouse: dispersion of TGF-beta gene family.
DE Barton, BE Foellmer, J Du, J Tamm, R Derynck, U Francke
Oncogene research 3 (4), 323-331, 1988
1551988
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)
M Claustres, V Kožich, E Dequeker, B Fowler, JY Hehir-Kwa, K Miller, ...
European journal of human genetics 22 (2), 160-170, 2014
1532014
Genetic drivers of kidney defects in the DiGeorge syndrome
E Lopez-Rivera, YP Liu, M Verbitsky, BR Anderson, VP Capone, EA Otto, ...
New England Journal of Medicine 376 (8), 742-754, 2017
1432017
Chromosome mapping of the growth hormone receptor gene in man and mouse
DE Barton, BE Foellmer, WI Wood, U Francke
Cytogenetic and Genome Research 50 (2-3), 137-141, 1989
1341989
Mapping of genes for inhibin subunits α, βA, and βB on human and mouse chromosomes and studies of jsd mice
DE Barton, TL Yang-Feng, AJ Mason, PH Seeburg, U Francke
Genomics 5 (1), 91-99, 1989
1291989
Quality control in molecular genetic testing
E Dequeker, S Ramsden, WW Grody, TT Stenzel, DE Barton
Nature Reviews Genetics 2 (9), 717-723, 2001
1262001
Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma
RM Irving, DA Moffat, DG Hardy, DE Barton, JH Xuereb, ER Maher
Human molecular genetics 3 (2), 347-350, 1994
1261994
Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
RE Slatter, M Elliott, K Welham, M Carrera, PN Schofield, DE Barton, ...
Journal of medical genetics 31 (10), 749-753, 1994
1241994
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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