Ben F Koop
Cited by
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Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
A Brooks-Wilson, M Marcil, SM Clee, LH Zhang, K Roomp, M van Dam, ...
Nature genetics 22 (4), 336-345, 1999
The Atlantic salmon genome provides insights into rediploidization
S Lien, BF Koop, SR Sandve, JR Miller, MP Kent, T Nome, TR Hvidsten, ...
Nature 533 (7602), 200-205, 2016
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
E Belloni, M Muenke, E Roessler, G Traverse, J Siegel-Bartelt, A Frumkin, ...
Nature genetics 14 (3), 353-356, 1996
Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11. 23 cause incomplete X-linked congenital stationary night blindness
NT Bech-Hansen, MJ Naylor, TA Maybaum, WG Pearce, B Koop, ...
Nature genetics 19 (3), 264-267, 1998
The complete 685-kilobase DNA sequence of the human β T cell receptor locus
L Rowen, BF Koop, L Hood
Science 272 (5269), 1755-1762, 1996
Large-scale and automated DNA sequence determination
T Hunkapiller, RJ Kaiser, BF Koop, L Hood
Science 254 (5028), 59-67, 1991
Embryonic ε and γ globin genes of a prosimian primate (Galago crassicaudatus): Nucleotide and amino acid sequences, developmental regulation and phylogenetic footprints
DA Tagle, BF Koop, M Goodman, JL Slightom, DL Hess, RT Jones
Journal of molecular biology 203 (2), 439-455, 1988
Cell death attenuation byUsurpin', a mammalian DED-caspase homologue that precludes caspase-8 recruitment and activation by the CD-95 (Fas, APO-1) receptor complex
DM Rasper, JP Vaillancourt, S Hadano, VM Houtzager, I Seiden, ...
Cell Death & Differentiation 5 (4), 271-288, 1998
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
NT Bech-Hansen, MJ Naylor, TA Maybaum, RL Sparkes, B Koop, ...
Nature genetics 26 (3), 319-323, 2000
DNA sequence determination by hybridization: a strategy for efficient large-scale sequencing
R Drmanac, S Drmanac, Z Strezoska, T Paunesku, I Labat, M Zeremski, ...
Science 260 (5114), 1649-1652, 1993
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
AJ Mears, T Jordan, F Mirzayans, S Dubois, T Kume, M Parlee, R Ritch, ...
The American Journal of Human Genetics 63 (5), 1316-1328, 1998
Development and application of a salmonid EST database and cDNA microarray: data mining and interspecific hybridization characteristics
ML Rise, KR von Schalburg, GD Brown, MA Mawer, RH Devlin, N Kuipers, ...
Genome research 14 (3), 478-490, 2004
Sequencing the genome of the Atlantic salmon (Salmo salar)
WS Davidson, BF Koop, SJM Jones, P Iturra, R Vidal, A Maass, ...
Genome biology 11, 1-7, 2010
Human chromosome 7: DNA sequence and biology
SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ...
Science 300 (5620), 767-772, 2003
Primate η-globin DNA sequences and man's place among the great apes
BF Koop, M Goodman, P Xu, K Chan, JL Slightom
Nature 319 (6050), 234-238, 1986
Determinants of DNA sequence specificity of the androgen, progesterone, and glucocorticoid receptors: evidence for differential steroid receptor response elements
CC Nelson, SC Hendy, RJ Shukin, H Cheng, N Bruchovsky, BF Koop, ...
Molecular endocrinology 13 (12), 2090-2107, 1999
Isolation and characterization of coho salmon (Oncorhynchus kisutch) microsatellites and their use in other salmonids.
Molecular Ecology 7 (11), 1998
Chromosomal studies of South American bats and their systematic implications
RJ Baker, MW Haiduk, LW Robbins, A Cadena, BF Koop
Mammalian Biology in South America 4, 303-327, 1982
Fish and chips: various methodologies demonstrate utility of a 16,006-gene salmonid microarray
KR von Schalburg, ML Rise, GA Cooper, GD Brown, AR Gibbs, ...
BMC genomics 6, 1-8, 2005
Sex-dependent dominance maintains migration supergene in rainbow trout
DE Pearse, NJ Barson, T Nome, G Gao, MA Campbell, A Abadía-Cardoso, ...
Nature Ecology & Evolution 3, 1731–1742, 2019
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