-
1
-
-
0025879424
-
Complementary DNA sequencing: Expressed sequence tags and human genome project
-
Adams, M.D., J.M. Kelley, J.D. Gocayne, M. Dubnick, M.H. Polymeropoulos, H. Xiao, C.R. Merril, A. Wu, B. Olde, R.F. Moreno et al. 1991. Complementary DNA sequencing: Expressed sequence tags and human genome project. Science 252: 1651-1656.
-
(1991)
Science
, vol.252
, pp. 1651-1656
-
-
Adams, M.D.1
Kelley, J.M.2
Gocayne, J.D.3
Dubnick, M.4
Polymeropoulos, M.H.5
Xiao, H.6
Merril, C.R.7
Wu, A.8
Olde, B.9
Moreno, R.F.10
-
2
-
-
0027212772
-
Angiotensinogen: A candidate gene involved in preeclampsia?
-
Arngrimsson, R., S. Purandare, M. Connor, J.J. Walker, S. Bjornsson, F. Soubrier, Y.V. Kotelevtsev, R.T. Geirsson, and H. Bjornsson. 1993. Angiotensinogen: A candidate gene involved in preeclampsia? Nat. Genet. 4: 114-115.
-
(1993)
Nat. Genet.
, vol.4
, pp. 114-115
-
-
Arngrimsson, R.1
Purandare, S.2
Connor, M.3
Walker, J.J.4
Bjornsson, S.5
Soubrier, F.6
Kotelevtsev, Y.V.7
Geirsson, R.T.8
Bjornsson, H.9
-
3
-
-
0022556870
-
Human C1 inhibitor: Primary structure, cDNA cloning, and chromosomal localization
-
Bock, S.C., K. Skriver, E. Nielsen, H.C. Thogersen, B. Wiman, V.H. Donaldson, R.L. Eddy, J. Marrinan, E. Radziejewska, R. Huber et al. 1986. Human C1 inhibitor: Primary structure, cDNA cloning, and chromosomal localization. Biochemistry 25: 4292-4301.
-
(1986)
Biochemistry
, vol.25
, pp. 4292-4301
-
-
Bock, S.C.1
Skriver, K.2
Nielsen, E.3
Thogersen, H.C.4
Wiman, B.5
Donaldson, V.H.6
Eddy, R.L.7
Marrinan, J.8
Radziejewska, E.9
Huber, R.10
-
4
-
-
0026703897
-
Molecular analysis of the gene for the human vitamin D-binding protein (group-specific component): Allelic differences of the common genetic GC types
-
Braun, A., R. Bichlmaier, and H. Cleve. 1992. Molecular analysis of the gene for the human vitamin D-binding protein (group-specific component): Allelic differences of the common genetic GC types. Hum. Genet. 89: 401-406.
-
(1992)
Hum. Genet.
, vol.89
, pp. 401-406
-
-
Braun, A.1
Bichlmaier, R.2
Cleve, H.3
-
5
-
-
0033018816
-
Reliable identification of large numbers of candidate SNPs from public EST data
-
Buetow, K.H., M.N. Edmonson, and A.B. Cassidy. 1999. Reliable identification of large numbers of candidate SNPs from public EST data. Nat. Genet. 21: 323-325.
-
(1999)
Nat. Genet.
, vol.21
, pp. 323-325
-
-
Buetow, K.H.1
Edmonson, M.N.2
Cassidy, A.B.3
-
6
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill M., D. Altshuler, J. Ireland, P. Sklar, K. Ardlie, N. Patil, C.R. Lane, E.P. Lim, N. Kalayanaraman, J. Nemesh et al. 1999. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat. Genet. 22: 231-238.
-
(1999)
Nat. Genet.
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Lane, C.R.7
Lim, E.P.8
Kalayanaraman, N.9
Nemesh, J.10
-
7
-
-
0030688004
-
Variations on a theme: Cataloging human DNA sequence variations
-
Collins, F.S., M.S. Guyer, and A. Chakravarti. 1997. Variations on a theme: Cataloging human DNA sequence variations. Science 278: 1580-1581.
-
(1997)
Science
, vol.278
, pp. 1580-1581
-
-
Collins, F.S.1
Guyer, M.S.2
Chakravarti, A.3
-
8
-
-
0025364861
-
The mutational spectrum of single base-pair substitutions causing human genetic disease: Patterns and predictions
-
Cooper, D.N. and M. Krawczak. 1990. The mutational spectrum of single base-pair substitutions causing human genetic disease: Patterns and predictions. Hum. Genet. 85: 55-74.
-
(1990)
Hum. Genet.
, vol.85
, pp. 55-74
-
-
Cooper, D.N.1
Krawczak, M.2
-
9
-
-
0023853921
-
The CpG dinucleotide and human genetic disease
-
Cooper, D.N. and H. Youssoufian. 1988. The CpG dinucleotide and human genetic disease. Hum. Genet. 78: 151-155.
-
(1988)
Hum. Genet.
, vol.78
, pp. 151-155
-
-
Cooper, D.N.1
Youssoufian, H.2
-
10
-
-
0027518279
-
Current methods of mutation detection
-
Cotton, R.G. 1993. Current methods of mutation detection. Mutat. Res. 285: 125-144.
-
(1993)
Mutat. Res.
, vol.285
, pp. 125-144
-
-
Cotton, R.G.1
-
11
-
-
0031978181
-
Base-calling of automated sequencer traces using phred. II. Error probabilities
-
Ewing, B. and P. Green. 1998. Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res. 8: 186-194.
-
(1998)
Genome Res.
, vol.8
, pp. 186-194
-
-
Ewing, B.1
Green, P.2
-
12
-
-
0031955518
-
Base-calling of automated sequencer traces using phred. I. Accuracy assessment
-
Ewing, B., L. Hillier, M.C. Wendl, and P. Green. 1998. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. Genome Res. 8: 175-185.
-
(1998)
Genome Res.
, vol.8
, pp. 175-185
-
-
Ewing, B.1
Hillier, L.2
Wendl, M.C.3
Green, P.4
-
13
-
-
0030471309
-
It's the genes EST access to human genome content
-
Gerhold, D. and C.T. Caskey. 1996. It's the genes EST access to human genome content. BioEssays 18: 973-981.
-
(1996)
BioEssays
, vol.18
, pp. 973-981
-
-
Gerhold, D.1
Caskey, C.T.2
-
14
-
-
0031955116
-
Consed: A graphical tool for sequence finishing
-
Gordon, D., C. Abajian, and P. Green. 1998. Consed: A graphical tool for sequence finishing. Genome Res. 8: 195-202.
-
(1998)
Genome Res.
, vol.8
, pp. 195-202
-
-
Gordon, D.1
Abajian, C.2
Green, P.3
-
15
-
-
84871926999
-
-
Green, P. 1993. cross_match (http://www.genome.washington.edu/ UWGC/analysistools/phrap.htm).
-
(1993)
Cross_Match
-
-
Green, P.1
-
16
-
-
0345409101
-
-
Green, P. 1994. phrap (http://www.genome.washington.edu/UWGC/ analysistools/phrap.htm).
-
(1994)
Phrap
-
-
Green, P.1
-
17
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood pressure homeostasis
-
Halushka, M.K., J.B. Fan, K. Bentley, L. Hsie, N. Shen, A. Weder, R. Cooper, R. Lipshutz, and A. Chakravarti. 1999. Patterns of single-nucleotide polymorphisms in candidate genes for blood pressure homeostasis. Nat. Genet. 22: 239-247.
-
(1999)
Nat. Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
18
-
-
0030949513
-
Archaic African and Asian lineages in the genetic ancestry of modern humans
-
Harding, R.M., S.M. Fullerton, R.C. Griffiths, J. Bond, M.J. Cox, J.A. Schneider, D.S. Moulin, and J.B. Clegg. 1997. Archaic African and Asian lineages in the genetic ancestry of modern humans. Am. J. Hum. Genet. 60: 772-789.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 772-789
-
-
Harding, R.M.1
Fullerton, S.M.2
Griffiths, R.C.3
Bond, J.4
Cox, M.J.5
Schneider, J.A.6
Moulin, D.S.7
Clegg, J.B.8
-
19
-
-
16144364414
-
Generation and analysis of 280,000 human expressed sequence tags
-
Hillier, L., G. Lennon, M. Becker, M.F. Bonaldo, B. Chiapelli, S. Chissoe, N. Dietrich, T. DuBuque, A. Favello, W. Gish et al. 1996. Generation and analysis of 280,000 human expressed sequence tags. Genome Res. 6: 807-828.
-
(1996)
Genome Res.
, vol.6
, pp. 807-828
-
-
Hillier, L.1
Lennon, G.2
Becker, M.3
Bonaldo, M.F.4
Chiapelli, B.5
Chissoe, S.6
Dietrich, N.7
DuBuque, T.8
Favello, A.9
Gish, W.10
-
20
-
-
0026669336
-
Molecular basis of human hypertension: Role of angiotensinogen
-
Jeunemaitre, X., F. Soubrier, Y.V. Kotelevtsev, R.P. Lifton, C.S. Williams, A. Charru, S.C. Hunt, P.N. Hopkins, R.R. Williams, J.M. Lalouel, and P. Corvolt. 1992. Molecular basis of human hypertension: Role of angiotensinogen. Cell 71: 169-180.
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
Soubrier, F.2
Kotelevtsev, Y.V.3
Lifton, R.P.4
Williams, C.S.5
Charru, A.6
Hunt, S.C.7
Hopkins, P.N.8
Williams, R.R.9
Lalouel, J.M.10
Corvolt, P.11
-
21
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatrie disorders
-
Lachman, H.M., D.F. Papolos, T. Saito, Y.M. Yu, C.L. Szumlanski, and R.M. Weinshilboum. 1996. Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatrie disorders. Pharmacogenetics 6: 243-250.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 243-250
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
Yu, Y.M.4
Szumlanski, C.L.5
Weinshilboum, R.M.6
-
22
-
-
9844220856
-
Catechol-O-methyltransferase Val158Met polymorphism: Frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder
-
Li, T., H. Vallada, D. Curtis, M. Arranz, K. Xu, G. Cai, H. Deng, J. Liu, R. Murray, X. Liu, and D.A. Collier. 1997. Catechol-O-methyltransferase Val158Met polymorphism: Frequency analysis in Han Chinese subjects and allelic association of the low activity allele with bipolar affective disorder. Pharmacogenetics 7: 349-353.
-
(1997)
Pharmacogenetics
, vol.7
, pp. 349-353
-
-
Li, T.1
Vallada, H.2
Curtis, D.3
Arranz, M.4
Xu, K.5
Cai, G.6
Deng, H.7
Liu, J.8
Murray, R.9
Liu, X.10
Collier, D.A.11
-
23
-
-
0024514325
-
Human insulin-like growth-factor-binding protein. Low-molecular-mass form: Protein sequence and cDNA cloning
-
Luthman, H., J. Soderling-Barros, B. Persson, C. Engberg, I. Stern, M. Lake, S.A. Franzen, M. Israelsson, B. Raden, B. Lindgren et al. 1989. Human insulin-like growth-factor-binding protein. Low-molecular-mass form: Protein sequence and cDNA cloning. Eur. J. Biochem. 180: 259-265.
-
(1989)
Eur. J. Biochem.
, vol.180
, pp. 259-265
-
-
Luthman, H.1
Soderling-Barros, J.2
Persson, B.3
Engberg, C.4
Stern, I.5
Lake, M.6
Franzen, S.A.7
Israelsson, M.8
Raden, B.9
Lindgren, B.10
-
24
-
-
0033024475
-
Angiotensinogen thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first trimester decidua. 1999
-
Morgan, T., C. Craven, J.M. Lalouel, and K. Ward. 1999. Angiotensinogen thr235 variant is associated with abnormal physiologic change of the uterine spiral arteries in first trimester decidua. 1999. Am. J. Obstet. Gynecol. 180: 95-102.
-
(1999)
Am. J. Obstet. Gynecol.
, vol.180
, pp. 95-102
-
-
Morgan, T.1
Craven, C.2
Lalouel, J.M.3
Ward, K.4
-
25
-
-
17344364213
-
DNA sequence diversity in a 9.7 kb region of the human lipoprotein lipase gene
-
Nickerson, D.A., S.L. Taylor, K.M. Weiss, A.G. Clark, R.G. Hutchinson, J. Stengard, V. Salomaa, E. Vartiainen, E. Boerwinkle, and C.F. Sing. 1998. DNA sequence diversity in a 9.7 kb region of the human lipoprotein lipase gene. Nat. Genet. 19: 233-240.
-
(1998)
Nat. Genet.
, vol.19
, pp. 233-240
-
-
Nickerson, D.A.1
Taylor, S.L.2
Weiss, K.M.3
Clark, A.G.4
Hutchinson, R.G.5
Stengard, J.6
Salomaa, V.7
Vartiainen, E.8
Boerwinkle, E.9
Sing, C.F.10
-
26
-
-
0031060620
-
Molecular evidence for human alpha2-HS glycoprotein (AHSG) polymorphism
-
Osawa, M., K. Umetsu, T. Okhi, T. Nagasawa, T. Suzuki, and S. Takeichi. 1997. Molecular evidence for human alpha2-HS glycoprotein (AHSG) polymorphism. Hum. Genet. 99: 18-21.
-
(1997)
Hum. Genet.
, vol.99
, pp. 18-21
-
-
Osawa, M.1
Umetsu, K.2
Okhi, T.3
Nagasawa, T.4
Suzuki, T.5
Takeichi, S.6
-
27
-
-
0033015046
-
Mining SNPs from EST databases
-
Picoult-Newberg, L., T.E. Ideker, M.G. Pohl, S.L. Taylor, M.A. Donaldson, D.A. Nickerson, and M. Boyce-Jacino. 1999. Mining SNPs from EST databases. Genome Res. 9: 167-174.
-
(1999)
Genome Res.
, vol.9
, pp. 167-174
-
-
Picoult-Newberg, L.1
Ideker, T.E.2
Pohl, M.G.3
Taylor, S.L.4
Donaldson, M.A.5
Nickerson, D.A.6
Boyce-Jacino, M.7
-
28
-
-
0027328108
-
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease
-
Poller, W., J.P. Faber, S. Weidinger, K. Tief, S. Scholz, M. Fischer, K. Olek, M. Kirchgesser, and H.H. Heidtmann. 1993. A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease, Genomics 17: 740-743.
-
(1993)
Genomics
, vol.17
, pp. 740-743
-
-
Poller, W.1
Faber, J.P.2
Weidinger, S.3
Tief, K.4
Scholz, S.5
Fischer, M.6
Olek, K.7
Kirchgesser, M.8
Heidtmann, H.H.9
-
29
-
-
0029866943
-
Optimized heterologous expression of the human zinc enzyme glyoxalase I
-
Ridderstrom, M. and B. Mannervik. 1996. Optimized heterologous expression of the human zinc enzyme glyoxalase I. Biochem. J. 314: 463-467.
-
(1996)
Biochem. J.
, vol.314
, pp. 463-467
-
-
Ridderstrom, M.1
Mannervik, B.2
-
30
-
-
0029863215
-
On signal sequence polymorphisms and diseases of distribution
-
Rosenblum, J.S., N.B. Gilula, and R.A. Lerner. 1996. On signal sequence polymorphisms and diseases of distribution. Proc. Natl. Acad. Sci. 93: 4471-4473.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 4471-4473
-
-
Rosenblum, J.S.1
Gilula, N.B.2
Lerner, R.A.3
-
31
-
-
0027310143
-
Human beta 2-glycoprotein I : Molecular analysis of DNA and amino acid polymorphisms
-
Steinkasserer, A., C. Dorner, R. Wurzner, and R.B. Sim. 1993. Human beta 2-glycoprotein I : Molecular analysis of DNA and amino acid polymorphisms. Hum. Genet. 91: 401-402.
-
(1993)
Hum. Genet.
, vol.91
, pp. 401-402
-
-
Steinkasserer, A.1
Dorner, C.2
Wurzner, R.3
Sim, R.B.4
-
32
-
-
0031669184
-
Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms
-
Taillon-Miller, P., Z. Gu, Q. Li, L. Hillier, and P.Y. Kwok. 1998. Overlapping genomic sequences: A treasure trove of single-nucleotide polymorphisms. Genome Res. 8: 748-754.
-
(1998)
Genome Res.
, vol.8
, pp. 748-754
-
-
Taillon-Miller, P.1
Gu, Z.2
Li, Q.3
Hillier, L.4
Kwok, P.Y.5
-
33
-
-
0028069840
-
Amino acid polymorphisms of the human L-isoaspartyl/D-aspartyl methyltransferase involved in protein repair
-
Tsai, W. and S. Clarke. 1994. Amino acid polymorphisms of the human L-isoaspartyl/D-aspartyl methyltransferase involved in protein repair. Biochem. Biophys. Res. Commun. 203: 491-497.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.203
, pp. 491-497
-
-
Tsai, W.1
Clarke, S.2
-
34
-
-
0025368579
-
Structural analysis of human apolipoprotein A-I variants: Amino acid substitutions are nonrandomly distributed throughout the apolipoprotein A-I primary structure
-
von Eckardstein, A., H. Funke, M. Walter, K. Altland, A. Benninghoven, and G. Assmann. 1990. Structural analysis of human apolipoprotein A-I variants: Amino acid substitutions are nonrandomly distributed throughout the apolipoprotein A-I primary structure. J. Biol. Chem. 265: 8610-8617.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 8610-8617
-
-
Von Eckardstein, A.1
Funke, H.2
Walter, M.3
Altland, K.4
Benninghoven, A.5
Assmann, G.6
-
35
-
-
0032524383
-
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
-
Wang, D.G., J.B. Fan, C. Siao, A. Berno, P. Young, R. Sapolsky, G. Ghandour, N. Perkins, E. Winchester, J. Spencer et al. 1998. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 280: 1077-1082.
-
(1998)
Science
, vol.280
, pp. 1077-1082
-
-
Wang, D.G.1
Fan, J.B.2
Siao, C.3
Berno, A.4
Young, P.5
Sapolsky, R.6
Ghandour, G.7
Perkins, N.8
Winchester, E.9
Spencer, J.10
-
36
-
-
0028789932
-
Polymorphisms and probable lack of mutation in a human mutt homolog, hMTH1, in hereditary nonpoliposis colorectal cancer
-
Wu, C., H. Nagasaki, K. Maruyama, Y. Nakabeppu, M. Sekiguchi, and Y. Yuasa. 1995. Polymorphisms and probable lack of mutation in a human mutT homolog, hMTH1, in hereditary nonpoliposis colorectal cancer. Biochem. Biophys. Res. Commun. 214: 1239-1245.
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.214
, pp. 1239-1245
-
-
Wu, C.1
Nagasaki, H.2
Maruyama, K.3
Nakabeppu, Y.4
Sekiguchi, M.5
Yuasa, Y.6
|