-
1
-
-
58149189856
-
McKusick's Online Mendelian Inheritance in Man (OMIM)
-
Amberger, J., Bocchini, C.A., Scott, A.F. and Hamosh, A. 2009, McKusick's Online Mendelian Inheritance in Man (OMIM), Nucleic Acids Res., 37, D793-6.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Amberger, J.1
Bocchini, C.A.2
Scott, A.F.3
Hamosh, A.4
-
2
-
-
4444379717
-
Primary immunodeficiency diseases: An update
-
Notarangelo, L., Casanova, J.L., Fischer, A., et al. 2004, Primary immunodeficiency diseases: an update, J. Allergy Clin. Immunol., 114, 677-687
-
(2004)
J. Allergy Clin. Immunol.
, vol.114
, pp. 677-687
-
-
Notarangelo, L.1
Casanova, J.L.2
Fischer, A.3
-
3
-
-
34948872289
-
Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee
-
Geha, R.S., Notarangelo, L.D., Casanova, J.L., et al. 2007, Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee, J. Allergy Clin. Immunol., 120, 776-794
-
(2007)
J. Allergy Clin. Immunol.
, vol.120
, pp. 776-794
-
-
Geha, R.S.1
Notarangelo, L.D.2
Casanova, J.L.3
-
4
-
-
57149138835
-
Is it necessary to identify molecular defects in primary immunodeficiency disease?
-
Notarangelo, L.D. and Sorensen, R. 2008, Is it necessary to identify molecular defects in primary immunodeficiency disease?, J. Allergy Clin. Immunol, 122, 1069-1073
-
(2008)
J. Allergy Clin. Immunol
, vol.122
, pp. 1069-1073
-
-
Notarangelo, L.D.1
Sorensen, R.2
-
5
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer, K.A., Ballinger, D.G., Cox, D.R., et al. 2007, A second generation human haplotype map of over 3.1 million SNPs, Nature, 449, 851-861
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
-
6
-
-
62649084535
-
Power of deep, all-exon resequen-cing for discovery of human trait genes
-
Kryukov, G.V., Shpunt, A., Stamatoyannopoulos, J.A. and Sunyaev, S.R. 2009, Power of deep, all-exon resequen-cing for discovery of human trait genes, Proc. Natl Acad. Sci. USA, 106, 3871-3876
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 3871-3876
-
-
Kryukov, G.V.1
Shpunt, A.2
Stamatoyannopoulos, J.A.3
Sunyaev, S.R.4
-
7
-
-
69749122314
-
Identification of deleterious mutations within three human genomes
-
Chun, S. and Fay, J.C. 2009, Identification of deleterious mutations within three human genomes, Genome Res., 19, 1553-1561
-
(2009)
Genome Res.
, vol.19
, pp. 1553-1561
-
-
Chun, S.1
Fay, J.C.2
-
8
-
-
0035869223
-
Prediction of deleterious human alleles
-
Sunyaev, S., Ramensky, V., Koch, I., Lathe, W. III, Kondrashov, A.S. and Bork, P. 2001, Prediction of deleterious human alleles, Hum. Mol. Genet., 10, 591-597
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 591-597
-
-
Sunyaev, S.1
Ramensky, V.2
Koch, I.3
Lathe Iii, W.4
Kondrashov, A.S.5
Bork, P.6
-
9
-
-
55549147204
-
Classification of rare missense substitutions, using risk surfaces, with genetic-and molecular-epidemiology applications
-
Tavtigian, S.V., Byrnes, G.B., Goldgar, D.E. and Thomas, A. 2008, Classification of rare missense substitutions, using risk surfaces, with genetic-and molecular-epidemiology applications, Hum. Mutat., 29, 1342-1354
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1342-1354
-
-
Tavtigian, S.V.1
Byrnes, G.B.2
Goldgar, D.E.3
Thomas, A.4
-
10
-
-
55549111626
-
Assessing pathogenicity: Overview of results from the IARC Unclassified Genetic Variants Working Group
-
Tavtigian, S.V., Greenblatt, M.S., Goldgar, D.E. and Boffetta, P. 2008, Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group, Hum. Mutat., 29, 1261-1264
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1261-1264
-
-
Tavtigian, S.V.1
Greenblatt, M.S.2
Goldgar, D.E.3
Boffetta, P.4
-
11
-
-
55549145156
-
In silico analysis of missense substitutions using sequence-alignment based methods
-
Tavtigian, S.V., Greenblatt, M.S., Lesueur, F. and Byrnes, G.B. 2008, In silico analysis of missense substitutions using sequence-alignment based methods, Hum. Mutat., 29, 1327-1336
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1327-1336
-
-
Tavtigian, S.V.1
Greenblatt, M.S.2
Lesueur, F.3
Byrnes, G.B.4
-
12
-
-
46749098393
-
Evaluation of in silico splice tools for decision-making in molecular diagnosis
-
Houdayer, C., Dehainault, C., Mattler, C., et al. 2008, Evaluation of in silico splice tools for decision-making in molecular diagnosis, Hum. Mutat., 29, 975-982
-
(2008)
Hum. Mutat.
, vol.29
, pp. 975-982
-
-
Houdayer, C.1
Dehainault, C.2
Mattler, C.3
-
13
-
-
77953446523
-
The Human Gene Mutation Database: 2008 update
-
Stenson, P.D., Mort, M., Ball, E.V., et al. 2009, The Human Gene Mutation Database: 2008 update, Genome Med., 1, 13.
-
(2009)
Genome Med.
, vol.1
, pp. 13
-
-
Stenson, P.D.1
Mort, M.2
Ball, E.V.3
-
14
-
-
38549119530
-
MutDB: Update on development of tools for the biochemical analysis of genetic variation
-
Singh, A., Olowoyeye, A., Baenziger, P.H., et al. 2008, MutDB: update on development of tools for the biochemical analysis of genetic variation, Nucleic Acids Res., 36, D815-9.
-
(2008)
Nucleic Acids Res.
, vol.36
-
-
Singh, A.1
Olowoyeye, A.2
Baenziger, P.H.3
-
15
-
-
34748848639
-
The NCBI dbGaP database of genotypes and phenotypes
-
Mailman, M.D., Feolo, M., Jin, Y., et al. 2007, The NCBI dbGaP database of genotypes and phenotypes, Nat. Genet., 39, 1181-1186
-
(2007)
Nat. Genet.
, vol.39
, pp. 1181-1186
-
-
Mailman, M.D.1
Feolo, M.2
Jin, Y.3
-
16
-
-
33751011339
-
Immunodeficiency mutation databases (IDbases)
-
Piirila, H., Valiaho, J. and Vihinen, M. 2006, Immunodeficiency mutation databases (IDbases), Hum. Mutat., 27, 1200-1208
-
(2006)
Hum. Mutat.
, vol.27
, pp. 1200-1208
-
-
Piirila, H.1
Valiaho, J.2
Vihinen, M.3
-
17
-
-
58149177158
-
RAPID: Resource of Asian Primary Immunodeficiency Diseases
-
Keerthikumar, S., Raju, R., Kandasamy, K., et al. 2009, RAPID: Resource of Asian Primary Immunodeficiency Diseases, Nucleic Acids Res., 37, D863-7.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Keerthikumar, S.1
Raju, R.2
Kandasamy, K.3
-
18
-
-
0035173378
-
DbSNP: The NCBI database of genetic variation
-
Sherry, S.T., Ward, M.H., Kholodov, M., et al. 2001, dbSNP: the NCBI database of genetic variation, Nucleic Acids Res., 29, 308-311
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.H.2
Kholodov, M.3
-
19
-
-
63749103607
-
Planning the human variome project: The Spain report
-
Kaput, J., Cotton, R.G., Hardman, L., et al. 2009, Planning the human variome project: the Spain report, Hum. Mutat., 30, 496-510.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 496-510
-
-
Kaput, J.1
Cotton, R.G.2
Hardman, L.3
-
20
-
-
38549158538
-
F-SNP: Computationally predicted functional SNPs for disease association studies
-
Lee, P.H. and Shatkay, H. 2008, F-SNP: computationally predicted functional SNPs for disease association studies, Nucleic Acids Res., 36, D820-4.
-
(2008)
Nucleic Acids Res.
, vol.36
-
-
Lee, P.H.1
Shatkay, H.2
-
21
-
-
33747832183
-
FASTSNP: An always up-to-date and extendable service for SNP function analysis and prioritization
-
Yuan, H.Y., Chiou, J.J., Tseng, W.H., et al. 2006, FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization, Nucleic Acids Res., 34, W635-41.
-
(2006)
Nucleic Acids Res.
, vol.34
-
-
Yuan, H.Y.1
Chiou, J.J.2
Tseng, W.H.3
-
22
-
-
33645764714
-
SNPs3D: Candidate gene and SNP selection for association studies
-
Yue, P., Melamud, E. and Moult, J. 2006, SNPs3D: candidate gene and SNP selection for association studies, BMC Bioinformatics, 7, 166.
-
(2006)
BMC Bioinformatics
, vol.7
, pp. 166
-
-
Yue, P.1
Melamud, E.2
Moult, J.3
-
23
-
-
61449107734
-
SNPnexus: A web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms
-
Chelala, C., Khan, A. and Lemoine, N.R. 2009, SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms, Bioinformatics, 25, 655-661
-
(2009)
Bioinformatics
, vol.25
, pp. 655-661
-
-
Chelala, C.1
Khan, A.2
Lemoine, N.R.3
-
24
-
-
57649232146
-
An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases
-
Yang, J.O., Hwang, S., Oh, J., Bhak, J. and Sohn, T.K. 2008, An integrated database-pipeline system for studying single nucleotide polymorphisms and diseases, BMC Bioinformatics, 9 (Suppl 12), S19.
-
(2008)
BMC Bioinformatics
, vol.9
, Issue.SUPPL. 12
-
-
Yang, J.O.1
Hwang, S.2
J, O.H.3
Bhak, J.4
Sohn, T.K.5
-
25
-
-
0345363156
-
Genatlas database, genes and development defects
-
Frezal, J. 1998, Genatlas database, genes and development defects, C. R. Acad. Sci. III, 321, 805-817
-
(1998)
C. R. Acad. Sci.
, vol.3
, Issue.321
, pp. 805-817
-
-
Frezal, J.1
-
26
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
Ng, P.C. and Henikoff, S. 2003, SIFT: predicting amino acid changes that affect protein function, Nucleic Acids Res., 31, 3812-3814
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
27
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky, V., Bork, P. and Sunyaev, S. 2002, Human non-synonymous SNPs: server and survey, Nucleic Acids Res., 30, 3894-3900
-
(2002)
Nucleic Acids Res.
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
28
-
-
0141742293
-
PANTHER: A library of protein families and subfamilies indexed by function
-
Thomas, P.D., Campbell, M.J., Kejariwal, A., et al. 2003, PANTHER: a library of protein families and subfamilies indexed by function, Genome Res., 13, 2129-2141
-
(2003)
Genome Res.
, vol.13
, pp. 2129-2141
-
-
Thomas, P.D.1
Campbell, M.J.2
Kejariwal, A.3
-
29
-
-
34547100092
-
SNAP: Predict effect of non-synonymous polymorphisms on function
-
Bromberg, Y. and Rost, B. 2007, SNAP: predict effect of non-synonymous polymorphisms on function, Nucleic Acids Res., 35, 3823-3835
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 3823-3835
-
-
Bromberg, Y.1
Rost, B.2
-
30
-
-
25144496606
-
PMUT: A web-based tool for the annotation of pathological mutations on proteins
-
Ferrer-Costa, C., Gelpi, J.L., Zamakola, L., Parraga, I., de la Cruz, X. and Orozco, M. 2005, PMUT: a web-based tool for the annotation of pathological mutations on proteins, Bioinformatics, 21, 3176-3178
-
(2005)
Bioinformatics
, vol.21
, pp. 3176-3178
-
-
Ferrer-Costa, C.1
Gelpi, J.L.2
Zamakola, L.3
Parraga, I.4
De La Cruz, X.5
Orozco, M.6
-
31
-
-
23144437332
-
NsSNPAnalyzer: Identifying disease-associated nonsynonymous single nucleotide polymorphisms
-
Bao, L., Zhou, M. and Cui, Y. 2005, nsSNPAnalyzer: identifying disease-associated nonsynonymous single nucleotide polymorphisms, Nucleic Acids Res., 33, W480-2.
-
(2005)
Nucleic Acids Res.
, vol.33
-
-
Bao, L.1
Zhou, M.2
Cui, Y.3
-
32
-
-
65649108490
-
Pathogenic or not? and if so, then how? Studying the effects of missense mutations using bioinformatics methods
-
Thusberg, J. and Vihinen, M. 2009, Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods, Hum. Mutat., 30, 703-714
-
(2009)
Hum. Mutat.
, vol.30
, pp. 703-714
-
-
Thusberg, J.1
Vihinen, M.2
-
33
-
-
33750353461
-
Predicting the effects of amino acid substitutions on protein function
-
Ng, P.C. and Henikoff, S. 2006, Predicting the effects of amino acid substitutions on protein function, Annu. Rev. Genomics Hum. Genet., 7, 61-80.
-
(2006)
Annu. Rev. Genomics Hum. Genet.
, vol.7
, pp. 61-80
-
-
Ng, P.C.1
Henikoff, S.2
-
34
-
-
40549098736
-
UniProtKB/Swiss-Prot
-
Boutet, E., Lieberherr, D., Tognolli, M., Schneider, M. and Bairoch, A. 2007, UniProtKB/Swiss-Prot, Methods Mol. Biol., 406, 89-112.
-
(2007)
Methods Mol. Biol.
, vol.406
, pp. 89-112
-
-
Boutet, E.1
Lieberherr, D.2
Tognolli, M.3
Schneider, M.4
Bairoch, A.5
-
35
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S.F., Gish, W., Miller, W., Myers, E.W. and Lipman, D.J. 1990, Basic local alignment search tool, J. Mol. Biol., 215, 403-410
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
36
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson, J.D., Higgins, D.G. and Gibson, T.J. 1994, CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice, Nucleic Acids Res., 22, 4673-4680
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
37
-
-
0036616218
-
The protein data bank, acta crystallogr
-
Berman, H.M., Battistuz, T., Bhat, T.N., et al. 2002, The Protein Data Bank, Acta Crystallogr. D Biol. Crystallogr., 58, 899-907.
-
(2002)
D Biol. Crystallogr.
, vol.58
, pp. 899-907
-
-
Berman, H.M.1
Battistuz, T.2
Bhat, T.N.3
-
38
-
-
0033873929
-
Comparative protein structure modeling of genes and genomes
-
Marti-Renom, M.A., Stuart, A.C., Fiser, A., Sanchez, R., Melo, F. and Sali, A. 2000, Comparative protein structure modeling of genes and genomes, Annu. Rev. Biophys. Biomol. Struct., 29, 291-325.
-
(2000)
Annu. Rev. Biophys. Biomol. Struct.
, vol.29
, pp. 291-325
-
-
Marti-Renom, M.A.1
Stuart, A.C.2
Fiser, A.3
Sanchez, R.4
Melo, F.5
Sali, A.6
-
39
-
-
33749578940
-
Statistical potential for assessment and prediction of protein structures
-
Shen, M.Y. and Sali, A. 2006, Statistical potential for assessment and prediction of protein structures, Protein Sci., 15, 2507-2524
-
(2006)
Protein Sci.
, vol.15
, pp. 2507-2524
-
-
Shen, M.Y.1
Sali, A.2
-
40
-
-
0015866154
-
Environment and exposure to solvent of protein atoms. Lysozyme and insulin
-
Shrake, A. and Rupley, J.A. 1973, Environment and exposure to solvent of protein atoms. Lysozyme and insulin, J. Mol. Biol., 79, 351-371
-
(1973)
J. Mol. Biol.
, vol.79
, pp. 351-371
-
-
Shrake, A.1
Rupley, J.A.2
-
41
-
-
3242891318
-
The DISOPRED server for the prediction of protein disorder
-
Ward, J.J., McGuffin, L.J., Bryson, K., Buxton, B.F. and Jones, D.T. 2004, The DISOPRED server for the prediction of protein disorder, Bioinformatics, 20, 2138-2139
-
(2004)
Bioinformatics
, vol.20
, pp. 2138-2139
-
-
Ward, J.J.1
McGuffin, L.J.2
Bryson, K.3
Buxton, B.F.4
Jones, D.T.5
-
42
-
-
0034191958
-
Towards a structural basis of human non-synonymous single nucleotide polymorphisms
-
Sunyaev, S., Ramensky, V. and Bork, P. 2000, Towards a structural basis of human non-synonymous single nucleotide polymorphisms, Trends Genet., 16, 198-200.
-
(2000)
Trends Genet.
, vol.16
, pp. 198-200
-
-
Sunyaev, S.1
Ramensky, V.2
Bork, P.3
-
43
-
-
1542577828
-
The amino-acid mutational spectrum of human genetic disease
-
Vitkup, D., Sander, C. and Church, G.M. 2003, The amino-acid mutational spectrum of human genetic disease, Genome Biol., 4, R72.
-
(2003)
Genome Biol.
, vol.4
-
-
Vitkup, D.1
Sander, C.2
Church, G.M.3
-
44
-
-
0035065485
-
SNPs, protein structure, and disease
-
Wang, Z. and Moult, J. 2001, SNPs, protein structure, and disease, Hum. Mutat., 17, 263-270
-
(2001)
Hum. Mutat.
, vol.17
, pp. 263-270
-
-
Wang, Z.1
Moult, J.2
-
45
-
-
0036300807
-
Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties
-
Ferrer-Costa, C., Orozco, M. and de la Cruz, X. 2002, Characterization of disease-associated single amino acid polymorphisms in terms of sequence and structure properties, J. Mol. Biol., 315, 771-786
-
(2002)
J. Mol. Biol.
, vol.315
, pp. 771-786
-
-
Ferrer-Costa, C.1
Orozco, M.2
De La Cruz, X.3
-
46
-
-
38549146891
-
ColiSNP database server mapping nsSNPs on protein structures
-
Kono, H., Yuasa, T., Nishiue, S. and Yura, K. 2008, coliSNP database server mapping nsSNPs on protein structures, Nucleic Acids Res., 36, D409-13.
-
(2008)
Nucleic Acids Res.
, vol.36
-
-
Kono, H.1
Yuasa, T.2
Nishiue, S.3
Yura, K.4
-
47
-
-
33645778262
-
Conservation of intrinsic disorder in protein domains and families: I. A database of conserved predicted disordered regions
-
Chen, J.W., Romero, P., Uversky, V.N. and Dunker, A.K. 2006, Conservation of intrinsic disorder in protein domains and families: I. A database of conserved predicted disordered regions, J. Proteome Res., 5, 879-887
-
(2006)
J. Proteome Res.
, Issue.5
, pp. 879-887
-
-
Chen, J.W.1
Romero, P.2
Uversky, V.N.3
Dunker, A.K.4
-
48
-
-
45949108954
-
Protein interactions in human genetic diseases
-
Schuster-Bockler, B. and Bateman, A. 2008, Protein interactions in human genetic diseases, Genome Biol., 9, R9.
-
(2008)
Genome Biol.
, vol.9
-
-
Schuster-Bockler, B.1
Bateman, A.2
-
49
-
-
35348960378
-
STAT3 mutations in the hyper-IgE syndrome
-
Holland, S.M., DeLeo, F.R., Elloumi, H.Z., et al. 2007, STAT3 mutations in the hyper-IgE syndrome, N. Engl. J. Med., 357, 1608-1619
-
(2007)
N. Engl. J. Med.
, vol.357
, pp. 1608-1619
-
-
Holland, S.M.1
Deleo, F.R.2
Elloumi, H.Z.3
-
50
-
-
34548317417
-
Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome
-
Minegishi, Y., Saito, M., Tsuchiya, S., et al. 2007, Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome, Nature, 448, 1058-1062
-
(2007)
Nature
, vol.448
, pp. 1058-1062
-
-
Minegishi, Y.1
Saito, M.2
Tsuchiya, S.3
-
51
-
-
38549146894
-
The Pfam protein families database
-
Finn, R.D., Tate, J., Mistry, J., et al. 2008, The Pfam protein families database, Nucleic Acids Res., 36, D281-8.
-
(2008)
Nucleic Acids Res.
, vol.36
-
-
Finn, R.D.1
Tate, J.2
Mistry, J.3
-
52
-
-
75549088687
-
Database resources of the National Center for Biotechnology Information
-
Sayers, E.W., Barrett, T., Benson, D.A., et al. 2009, Database resources of the National Center for Biotechnology Information, Nucleic Acids Res., 37, D5-15.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Sayers, E.W.1
Barrett, T.2
Benson, D.A.3
-
53
-
-
58149193222
-
Human Protein Reference Database\2009 update
-
Keshava Prasad, T.S., Goel, R., Kandasamy, K., et al. 2009, Human Protein Reference Database\2009 update, Nucleic Acids Res., 37, D767-72.
-
(2009)
Nucleic Acids Res.
, vol.37
-
-
Keshava Prasad, T.S.1
Goel, R.2
Kandasamy, K.3
-
54
-
-
0031762950
-
GeneCards: A novel functional genomics compendium with automated data mining and query reformulation support
-
Rebhan, M., Chalifa-Caspi, V., Prilusky, J. and Lancet, D. 1998, GeneCards: a novel functional genomics compendium with automated data mining and query reformulation support, Bioinformatics, 14, 656-664
-
(1998)
Bioinformatics
, vol.14
, pp. 656-664
-
-
Rebhan, M.1
Chalifa-Caspi, V.2
Prilusky, J.3
Lancet, D.4
-
55
-
-
36448982836
-
Construction of an open-access database that integrates cross-reference information from the transcrip-tome and proteome of immune cells
-
Hijikata, A., Kitamura, H., Kimura, Y., et al. 2007, Construction of an open-access database that integrates cross-reference information from the transcrip-tome and proteome of immune cells, Bioinformatics, 23, 2934-2941
-
(2007)
Bioinformatics
, vol.23
, pp. 2934-2941
-
-
Hijikata, A.1
Kitamura, H.2
Kimura, Y.3
-
56
-
-
0033982936
-
KEGG: Kyoto encyclopedia of genes and genomes
-
Kanehisa, M. and Goto, S. 2000, KEGG: kyoto encyclopedia of genes and genomes, Nucleic Acids Res., 28, 27-30.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 27-30
-
-
Kanehisa, M.1
Goto, S.2
-
57
-
-
0032499801
-
Three-dimensional structure of the Stat3beta homodimer bound to DNA
-
Becker, S., Groner, B. and Muller, C.W. 1998, Three-dimensional structure of the Stat3beta homodimer bound to DNA, Nature, 394, 145-151
-
(1998)
Nature
, vol.394
, pp. 145-151
-
-
Becker, S.1
Groner, B.2
Muller, C.W.3
-
58
-
-
0036226603
-
BLAT\the BLAST-like alignment tool
-
Kent, W.J. 2002, BLAT\the BLAST-like alignment tool, Genome Res., 12, 656-664
-
(2002)
Genome Res.
, vol.12
, pp. 656-664
-
-
Kent, W.J.1
-
59
-
-
69749124820
-
The first Korean genome sequence and analysis: Full genome sequencing for a socio-ethnic group
-
Ahn, S.M., Kim, T.H., Lee, S., et al. 2009, The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group, Genome Res., 19, 1622-1629
-
(2009)
Genome Res.
, vol.19
, pp. 1622-1629
-
-
Ahn, S.M.1
Kim, T.H.2
Lee, S.3
|