David L Nelson
David L Nelson
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Initial sequencing and analysis of the human genome
US DOE Joint Genome Institute: Hawkins Trevor 4 Branscomb Elbert 4 Predki ...
nature 409 (6822), 860-921, 2001
Initial sequencing and comparative analysis of the mouse genome
European Bioinformatics Institute: Birney Ewan 3 Goldman Nick 3 Kasprzyk ...
Nature 420 (6915), 520-562, 2002
The Genome Sequence of Drosophila melanogaster
MD Adams, SE Celniker, RA Holt, CA Evans, JD Gocayne, ...
Science 287 (5461), 2185-2195, 2000
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
AJMH Verkerk, M Pieretti, JS Sutcliffe, YH Fu, DPA Kuhl, A Pizzuti, ...
Cell 65 (5), 905-914, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox
YH Fu, DPA Kuhl, A Pizzuti, M Pieretti, JS Sutcliffe, S Richards, ...
Cell 67 (6), 1047-1058, 1991
Absence of expression of the FMR-1 gene in fragile X syndrome
M Pieretti, F Zhang, YH Fu, ST Warren, BA Oostra, CT Caskey, DL Nelson
Cell 66 (4), 817-822, 1991
Evolutionary and biomedical insights from the rhesus macaque genome
RA Gibbs, J Rogers, MG Katze, R Bumgarner, GM Weinstock, ER Mardis, ...
science 316 (5822), 222-234, 2007
The DNA sequence of the human X chromosome
MT Ross, DV Grafham, AJ Coffey, S Scherer, K McLay, D Muzny, ...
Nature 434 (7031), 325-337, 2005
Genomic rearrangement in NEMO impairs NF-[kappa] B activation and is a cause of incontinentia pigmenti
A Smahi, G Courtois, P Vabres, S Yamaoka, S Heuertz, A Munnich, ...
Nature 405 (6785), 466-473, 2000
DNA methylation represses FMR-1 transcription in fragile X syndrome
JS Sutcliffe, DL Nelson, F Zhang, M Pieretti, CT Caskey, D Saxe, ...
Human molecular genetics 1 (6), 397-400, 1992
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources.
DL Nelson, SA Ledbetter, L Corbo, MF Victoria, R Ramírez-Solis, ...
Proceedings of the National Academy of Sciences 86 (17), 6686-6690, 1989
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
P Jin, DC Zarnescu, S Ceman, M Nakamoto, J Mowrey, TA Jongens, ...
Nature neuroscience 7 (2), 113-117, 2004
A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence
HH Chou, H Takematsu, S Diaz, J Iber, E Nickerson, KL Wright, ...
Proceedings of the National Academy of Sciences 95 (20), 11751-11756, 1998
Length of uninterrupted CGG repeats determines instability in the FMR1 gene
EE Eichler, JJA Holden, BW Popovich, AL Reiss, K Snow, SN Thibodeau, ...
Nature genetics 8 (1), 88-94, 1994
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, DL Burgess, A Rasmussen, RP Grewal, ...
Nature genetics 26 (2), 191-194, 2000
The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase
O Attree, IM Olivos, I Okabe, LC Bailey, DL Nelson, RA Lewis, ...
Nature 358 (6383), 239-242, 1992
Triplet repeat mutations in human disease
CT Caskey, A Pizzuti, YH Fu, RG Fenwick Jr, DL Nelson
Science 256 (5058), 784-789, 1992
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
HL Hinds, CT Ashley, JS Sutcliffe, DL Nelson, ST Warren, DE Housman, ...
Nature genetics 3 (1), 36-43, 1993
X-linked situs abnormalities result from mutations in ZIC3
M Gebbia, GB Ferrero, G Pilia, MT Bassi, AS Aylsworth, M Penman-Splitt, ...
Nature genetics 17 (3), 305-308, 1997
Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome
SKE Koekkoek, K Yamaguchi, BA Milojkovic, BR Dortland, TJH Ruigrok, ...
Neuron 47 (3), 339-352, 2005
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