-
1
-
-
41149121347
-
The evolution of mammalian gene families
-
doi:10.1371/journal.pone.0000085
-
Demuth JP, De Bie T, Stajich JE, Cristianini N, Hahn MW, (2006) The evolution of mammalian gene families. PLoS ONE 1: e85 doi:10.1371/journal.pone.0000085.
-
(2006)
PLoS ONE
, vol.1
-
-
Demuth, J.P.1
De Bie, T.2
Stajich, J.E.3
Cristianini, N.4
Hahn, M.W.5
-
2
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad DF, Pinto D, Redon R, Feuk L, Gokcumen O, et al. (2010) Origins and functional impact of copy number variation in the human genome. Nature 464: 704-712.
-
(2010)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
Feuk, L.4
Gokcumen, O.5
-
3
-
-
84860860685
-
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
-
Dennis MY, Nuttle X, Sudmant PH, Antonacci F, Graves TA, et al. (2012) Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication. Cell 149: 912-922.
-
(2012)
Cell
, vol.149
, pp. 912-922
-
-
Dennis, M.Y.1
Nuttle, X.2
Sudmant, P.H.3
Antonacci, F.4
Graves, T.A.5
-
4
-
-
84861532037
-
Exploring the role of copy number variants in human adaptation
-
Iskow RC, Gokcumen O, Lee C, (2012) Exploring the role of copy number variants in human adaptation. Trends Genet 28: 245-257.
-
(2012)
Trends Genet
, vol.28
, pp. 245-257
-
-
Iskow, R.C.1
Gokcumen, O.2
Lee, C.3
-
5
-
-
30744451158
-
Adaptive loss of an old duplicated gene during incipient speciation
-
Greenberg AJ, Moran JR, Fang S, Wu CI, (2006) Adaptive loss of an old duplicated gene during incipient speciation. Mol Biol Evol 23: 401-410.
-
(2006)
Mol Biol Evol
, vol.23
, pp. 401-410
-
-
Greenberg, A.J.1
Moran, J.R.2
Fang, S.3
Wu, C.I.4
-
6
-
-
0027905006
-
Natural selection and the origin of jingwei, a chimeric processed functional gene in Drosophila
-
Long MY, Langley CH, (1993) Natural selection and the origin of jingwei, a chimeric processed functional gene in Drosophila. Science 260: 91-95.
-
(1993)
Science
, vol.260
, pp. 91-95
-
-
Long, M.Y.1
Langley, C.H.2
-
7
-
-
56549119570
-
Turning a hobby into a job: How duplicated genes find new functions
-
Conant GC, Wolfe KH, (2008) Turning a hobby into a job: How duplicated genes find new functions. Nat Rev Genet 9: 938-950.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 938-950
-
-
Conant, G.C.1
Wolfe, K.H.2
-
8
-
-
66049128566
-
Distinguishing among evolutionary models for the maintenance of gene duplicates
-
Hahn MW, (2009) Distinguishing among evolutionary models for the maintenance of gene duplicates. J Hered 100: 605-617.
-
(2009)
J Hered
, vol.100
, pp. 605-617
-
-
Hahn, M.W.1
-
9
-
-
80755187820
-
Human copy number variation and complex genetic disease
-
Girirajan S, Campbell CD, Eichler EE, (2011) Human copy number variation and complex genetic disease. Annu Rev Genet 45: 203-226.
-
(2011)
Annu Rev Genet
, vol.45
, pp. 203-226
-
-
Girirajan, S.1
Campbell, C.D.2
Eichler, E.E.3
-
10
-
-
34347353237
-
Copy-number variation and association studies of human disease
-
McCarroll SA, Altshuler DM, (2007) Copy-number variation and association studies of human disease. Nat Genet 39: S37-S42.
-
(2007)
Nat Genet
, vol.39
-
-
McCarroll, S.A.1
Altshuler, D.M.2
-
11
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
Stankiewicz P, Lupski JR, (2010) Structural variation in the human genome and its role in disease. Annu Rev Med pp. 437-455.
-
(2010)
Annu Rev Med
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
12
-
-
43049143055
-
Mapping and sequencing of structural variation from eight human genomes
-
Kidd JM, Cooper GM, Donahue WF, Hayden HS, Sampas N, et al. (2008) Mapping and sequencing of structural variation from eight human genomes. Nature 453: 56-64.
-
(2008)
Nature
, vol.453
, pp. 56-64
-
-
Kidd, J.M.1
Cooper, G.M.2
Donahue, W.F.3
Hayden, H.S.4
Sampas, N.5
-
13
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, et al. (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40: 1166-1174.
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
Cawley, S.4
Nemesh, J.5
-
14
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R, Ishikawa S, Fitch KR, Feuk L, Perry GH, et al. (2006) Global variation in copy number in the human genome. Nature 444: 444-454.
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
-
15
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, et al. (2004) Large-scale copy number polymorphism in the human genome. Science 305: 525-528.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
-
16
-
-
57049101718
-
Comparative genomics of wild type yeast strains unveils important genome diversity
-
Carreto L, Eiriz MF, Gomes AC, Pereira PM, Schuller D, et al. (2008) Comparative genomics of wild type yeast strains unveils important genome diversity. BMC Genomics 9: 524.
-
(2008)
BMC Genomics
, vol.9
, pp. 524
-
-
Carreto, L.1
Eiriz, M.F.2
Gomes, A.C.3
Pereira, P.M.4
Schuller, D.5
-
17
-
-
46249105777
-
Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster
-
Emerson JJ, Cardoso-Moreira M, Borevitz JO, Long M, (2008) Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster. Science 320: 1629-1631.
-
(2008)
Science
, vol.320
, pp. 1629-1631
-
-
Emerson, J.J.1
Cardoso-Moreira, M.2
Borevitz, J.O.3
Long, M.4
-
18
-
-
57149099394
-
Sequencing of natural strains of Arabidopsis thaliana with short reads
-
Ossowski S, Schneeberger K, Clark RM, Lanz C, Warthmann N, et al. (2008) Sequencing of natural strains of Arabidopsis thaliana with short reads. Genome Res 18: 2024-2033.
-
(2008)
Genome Res
, vol.18
, pp. 2024-2033
-
-
Ossowski, S.1
Schneeberger, K.2
Clark, R.M.3
Lanz, C.4
Warthmann, N.5
-
20
-
-
0037047628
-
Recent segmental duplications in the human genome
-
Bailey JA, Gu ZP, Clark RA, Reinert K, Samonte RV, et al. (2002) Recent segmental duplications in the human genome. Science 297: 1003-1007.
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
Gu, Z.P.2
Clark, R.A.3
Reinert, K.4
Samonte, R.V.5
-
21
-
-
72649089957
-
Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications
-
Schrider DR, Hahn MW, (2010) Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications. Mol Biol Evol 27: 103-111.
-
(2010)
Mol Biol Evol
, vol.27
, pp. 103-111
-
-
Schrider, D.R.1
Hahn, M.W.2
-
22
-
-
0025864962
-
Retroposons - seeds of evolution
-
Brosius J, (1991) Retroposons- seeds of evolution. Science 251: 753-753.
-
(1991)
Science
, vol.251
, pp. 753
-
-
Brosius, J.1
-
23
-
-
27844557002
-
Emergence of young human genes after a burst of retroposition in primates
-
doi:10.1371/journal.pbio.0030357
-
Marques AC, Dupanloup I, Vinckenbosch N, Reymond A, Kaessmann H, (2005) Emergence of young human genes after a burst of retroposition in primates. PLoS Biol 3: e357 doi:10.1371/journal.pbio.0030357.
-
(2005)
PLoS Biol
, vol.3
-
-
Marques, A.C.1
Dupanloup, I.2
Vinckenbosch, N.3
Reymond, A.4
Kaessmann, H.5
-
24
-
-
44649083780
-
Retrotransposition as a source of new promoters
-
Okamura K, Nakai K, (2008) Retrotransposition as a source of new promoters. Mol Biol Evol 25: 1231-1238.
-
(2008)
Mol Biol Evol
, vol.25
, pp. 1231-1238
-
-
Okamura, K.1
Nakai, K.2
-
25
-
-
56449118064
-
Retrocopy contributions to the evolution of the human genome
-
Baertsch R, Diekhans M, Kent WJ, Haussler D, Brosius J, (2008) Retrocopy contributions to the evolution of the human genome. BMC Genomics 9.
-
(2008)
BMC Genomics
, vol.9
-
-
Baertsch, R.1
Diekhans, M.2
Kent, W.J.3
Haussler, D.4
Brosius, J.5
-
27
-
-
34147128526
-
Comparative genomics reveals a constant rate of origination and convergent acquisition of functional retrogenes in Drosophila
-
Bai YS, Casola C, Feschotte C, Betran E, (2007) Comparative genomics reveals a constant rate of origination and convergent acquisition of functional retrogenes in Drosophila. Genome Biol 8: R11.
-
(2007)
Genome Biol
, vol.8
-
-
Bai, Y.S.1
Casola, C.2
Feschotte, C.3
Betran, E.4
-
28
-
-
0036906987
-
Retroposed new genes out of the X in Drosophila
-
Betrán E, Thornton K, Long M, (2002) Retroposed new genes out of the X in Drosophila. Genome Res 12: 1854-1859.
-
(2002)
Genome Res
, vol.12
, pp. 1854-1859
-
-
Betrán, E.1
Thornton, K.2
Long, M.3
-
29
-
-
1642475221
-
Extensive gene traffic on the mammalian X chromosome
-
Emerson JJ, Kaessmann H, Betran E, Long MY, (2004) Extensive gene traffic on the mammalian X chromosome. Science 303: 537-540.
-
(2004)
Science
, vol.303
, pp. 537-540
-
-
Emerson, J.J.1
Kaessmann, H.2
Betran, E.3
Long, M.Y.4
-
30
-
-
83055168359
-
Genome-wide analysis of retrogene polymorphisms in Drosophila melanogaster
-
Schrider DR, Stevens K, Cardeno CM, Langley CH, Hahn MW, (2011) Genome-wide analysis of retrogene polymorphisms in Drosophila melanogaster. Genome Res 21: 2087-2095.
-
(2011)
Genome Res
, vol.21
, pp. 2087-2095
-
-
Schrider, D.R.1
Stevens, K.2
Cardeno, C.M.3
Langley, C.H.4
Hahn, M.W.5
-
31
-
-
84856793694
-
Pseudogene-mediated posttranscriptional silencing of HMGA1 can result in insulin resistance and type 2 diabetes
-
Chiefari E, Iiritano S, Paonessa F, Le Pera I, Arcidiacono B, et al. (2010) Pseudogene-mediated posttranscriptional silencing of HMGA1 can result in insulin resistance and type 2 diabetes. Nat Commun 1: 40.
-
(2010)
Nat Commun
, vol.1
, pp. 40
-
-
Chiefari, E.1
Iiritano, S.2
Paonessa, F.3
Le Pera, I.4
Arcidiacono, B.5
-
32
-
-
77953957633
-
A coding-independent function of gene and pseudogene mRNAs regulates tumour biology
-
Poliseno L, Salmena L, Zhang J, Carver B, Haveman WJ, et al. (2010) A coding-independent function of gene and pseudogene mRNAs regulates tumour biology. Nature 465: 1033-1038.
-
(2010)
Nature
, vol.465
, pp. 1033-1038
-
-
Poliseno, L.1
Salmena, L.2
Zhang, J.3
Carver, B.4
Haveman, W.J.5
-
33
-
-
84856409929
-
Detection of structural variants and indels within exome data
-
Karakoc E, Alkan C, O'Roak BJ, Dennis MY, Vives L, et al. (2011) Detection of structural variants and indels within exome data. Nat Methods 9: 176-178.
-
(2011)
Nat Methods
, vol.9
, pp. 176-178
-
-
Karakoc, E.1
Alkan, C.2
O'Roak, B.J.3
Dennis, M.Y.4
Vives, L.5
-
34
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Altshuler DL, Durbin RM, Abecasis GR, Bentley DR, Chakravarti A, et al. (2010) A map of human genome variation from population-scale sequencing. Nature 467: 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Altshuler, D.L.1
Durbin, R.M.2
Abecasis, G.R.3
Bentley, D.R.4
Chakravarti, A.5
-
35
-
-
43249118306
-
Chromosomal gene movements reflect the recent origin and biology of therian sex chromosomes
-
doi:10.1371/journal.pbio.0060080
-
Potrzebowski L, Vinckenbosch N, Marques AC, Chalmel F, Jegou B, et al. (2008) Chromosomal gene movements reflect the recent origin and biology of therian sex chromosomes. PLoS Biol 6: e80 doi:10.1371/journal.pbio.0060080.
-
(2008)
PLoS Biol
, vol.6
-
-
Potrzebowski, L.1
Vinckenbosch, N.2
Marques, A.C.3
Chalmel, F.4
Jegou, B.5
-
36
-
-
84861900818
-
Nuclear chromosome dynamics in the Drosophila male germ line contribute to the nonrandom genomic distribution of retrogenes
-
Diaz-Castillo C, Ranz JM, (2012) Nuclear chromosome dynamics in the Drosophila male germ line contribute to the nonrandom genomic distribution of retrogenes. Mol Biol Evol 29: 2105-2108.
-
(2012)
Mol Biol Evol
, vol.29
, pp. 2105-2108
-
-
Diaz-Castillo, C.1
Ranz, J.M.2
-
37
-
-
34250212945
-
Sense-antisense pairs in mammals: functional and evolutionary considerations
-
Galante PAF, Vidal DO, de Souza JE, Camargo AA, de Souza SJ, (2007) Sense-antisense pairs in mammals: functional and evolutionary considerations. Genome Biol 8: R40.
-
(2007)
Genome Biol
, vol.8
-
-
Galante, P.A.F.1
Vidal, D.O.2
de Souza, J.E.3
Camargo, A.A.4
de Souza, S.J.5
-
38
-
-
66249132041
-
mRNA retrotransposition coupled with 5′ inversion as a possible source of new genes
-
Kojima KK, Okada N, (2009) mRNA retrotransposition coupled with 5′ inversion as a possible source of new genes. Mol Biol Evol 26: 1405-1420.
-
(2009)
Mol Biol Evol
, vol.26
, pp. 1405-1420
-
-
Kojima, K.K.1
Okada, N.2
-
39
-
-
84855870527
-
Chimeric genes as a source of rapid evolution in Drosophila melanogaster
-
Rogers RL, Hartl DL, (2011) Chimeric genes as a source of rapid evolution in Drosophila melanogaster. Mol Biol Evol 29: 517-529.
-
(2011)
Mol Biol Evol
, vol.29
, pp. 517-529
-
-
Rogers, R.L.1
Hartl, D.L.2
-
40
-
-
0035895567
-
Birth of two chimeric genes in the Hominidae lineage
-
Courseaux A, Nahon JL, (2001) Birth of two chimeric genes in the Hominidae lineage. Science 291: 1293-1297.
-
(2001)
Science
, vol.291
, pp. 1293-1297
-
-
Courseaux, A.1
Nahon, J.L.2
-
41
-
-
0033995607
-
Back to the roots of a new exon - The molecular archaeology of a SP100 splice variant
-
Rogalla P, Kazmierczak B, Flohr AM, Hauke S, Bullerdiek J, (2000) Back to the roots of a new exon- The molecular archaeology of a SP100 splice variant. Genomics 63: 117-122.
-
(2000)
Genomics
, vol.63
, pp. 117-122
-
-
Rogalla, P.1
Kazmierczak, B.2
Flohr, A.M.3
Hauke, S.4
Bullerdiek, J.5
-
42
-
-
20444420187
-
Origin and evolution of a chimeric fusion gene in Drosophila subobscura, D. madeirensis and D. guanche
-
Jones CD, Custer AW, Begun DJ, (2005) Origin and evolution of a chimeric fusion gene in Drosophila subobscura, D. madeirensis and D. guanche. Genetics 170: 207-219.
-
(2005)
Genetics
, vol.170
, pp. 207-219
-
-
Jones, C.D.1
Custer, A.W.2
Begun, D.J.3
-
43
-
-
0037007062
-
Origin of sphinx, a young chimeric RNA gene in Drosophila melanogaster
-
Wang W, Brunet FG, Nevo E, Long M, (2002) Origin of sphinx, a young chimeric RNA gene in Drosophila melanogaster. Proc Natl Acad Sci U S A 99: 4448-4453.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 4448-4453
-
-
Wang, W.1
Brunet, F.G.2
Nevo, E.3
Long, M.4
-
44
-
-
23844533589
-
Parallel evolution of chimeric fusion genes
-
Jones CD, Begun DJ, (2005) Parallel evolution of chimeric fusion genes. Proc Natl Acad Sci U S A 102: 11373-11378.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 11373-11378
-
-
Jones, C.D.1
Begun, D.J.2
-
45
-
-
77950458649
-
Transcriptome genetics using second generation sequencing in a Caucasian population
-
Montgomery SB, Sammeth M, Gutierrez-Arcelus M, Lach RP, Ingle C, et al. (2010) Transcriptome genetics using second generation sequencing in a Caucasian population. Nature 464: 773-U151.
-
(2010)
Nature
, vol.464
, pp. 151-773
-
-
Montgomery, S.B.1
Sammeth, M.2
Gutierrez-Arcelus, M.3
Lach, R.P.4
Ingle, C.5
-
46
-
-
80051709050
-
Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual
-
Galante PAF, Parmigiani RB, Zhao Q, Caballero OL, de Souza JE, et al. (2011) Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual. Nucleic Acids Res 39: 6056-6068.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 6056-6068
-
-
Galante, P.A.F.1
Parmigiani, R.B.2
Zhao, Q.3
Caballero, O.L.4
de Souza, J.E.5
-
47
-
-
35349012592
-
Genome-wide detection and characterization of positive selection in human populations
-
Sabeti PC, Varilly P, Fry B, Lohmueller J, Hostetter E, et al. (2007) Genome-wide detection and characterization of positive selection in human populations. Nature 449: 913-918.
-
(2007)
Nature
, vol.449
, pp. 913-918
-
-
Sabeti, P.C.1
Varilly, P.2
Fry, B.3
Lohmueller, J.4
Hostetter, E.5
-
48
-
-
33644981509
-
A map of recent positive selection in the human genome
-
doi:10.1371/journal.pbio.0040072
-
Voight BF, Kudaravalli S, Wen XQ, Pritchard JK, (2006) A map of recent positive selection in the human genome. PLoS Biol 4: e72 doi:10.1371/journal.pbio.0040072.
-
(2006)
PLoS Biol
, vol.4
-
-
Voight, B.F.1
Kudaravalli, S.2
Wen, X.Q.3
Pritchard, J.K.4
-
49
-
-
0022760782
-
On the divergence of alleles in nested subsamples from finite populations
-
Hudson RR, Kaplan NL, (1986) On the divergence of alleles in nested subsamples from finite populations. Genetics 113: 1057-1076.
-
(1986)
Genetics
, vol.113
, pp. 1057-1076
-
-
Hudson, R.R.1
Kaplan, N.L.2
-
50
-
-
0036184745
-
Generating samples under a Wright-Fisher neutral model of genetic variation
-
Hudson RR, (2002) Generating samples under a Wright-Fisher neutral model of genetic variation. Bioinformatics 18: 337-338.
-
(2002)
Bioinformatics
, vol.18
, pp. 337-338
-
-
Hudson, R.R.1
-
51
-
-
0028215929
-
Evidence for positive selection in the superoxide dismutase (Sod) region of Drosophila melanogaster
-
Hudson RR, Bailey K, Skarecky D, Kwiatowski J, Ayala FJ, (1994) Evidence for positive selection in the superoxide dismutase (Sod) region of Drosophila melanogaster. Genetics 136: 1329-1340.
-
(1994)
Genetics
, vol.136
, pp. 1329-1340
-
-
Hudson, R.R.1
Bailey, K.2
Skarecky, D.3
Kwiatowski, J.4
Ayala, F.J.5
-
52
-
-
0023943873
-
Chromosomal localization and racial distribution of the polymorphic human dihydrofolate-reductase pseudogene (DHFRPI)
-
Anagnou NP, Antonarakis SE, Obrien SJ, Modi WS, Nienhuis AW, (1988) Chromosomal localization and racial distribution of the polymorphic human dihydrofolate-reductase pseudogene (DHFRPI). Am J Hum Genet 42: 345-352.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 345-352
-
-
Anagnou, N.P.1
Antonarakis, S.E.2
Obrien, S.J.3
Modi, W.S.4
Nienhuis, A.W.5
-
53
-
-
80053060915
-
The former annotated human pseudogene dihydrofolate reductase-like 1 (DHFRL1) is expressed and functional
-
McEntee G, Minguzzi S, O'Brien K, Ben Larbi N, Loscher C, et al. (2011) The former annotated human pseudogene dihydrofolate reductase-like 1 (DHFRL1) is expressed and functional. Proc Natl Acad Sci U S A 108: 15157-15162.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 15157-15162
-
-
McEntee, G.1
Minguzzi, S.2
O'Brien, K.3
Ben Larbi, N.4
Loscher, C.5
-
54
-
-
79851500161
-
Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease
-
Cario H, Smith DEC, Blom H, Blau N, Bode H, et al. (2011) Dihydrofolate reductase deficiency due to a homozygous DHFR mutation causes megaloblastic anemia and cerebral folate deficiency leading to severe neurologic disease. Am J Hum Genet 88: 226-231.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 226-231
-
-
Cario, H.1
Smith, D.E.C.2
Blom, H.3
Blau, N.4
Bode, H.5
-
55
-
-
0001127374
-
Isolation of Chinese hamster cell mutants deficient in dihydrofolate reductase activity
-
Urlaub G, Chasin LA, (1980) Isolation of Chinese hamster cell mutants deficient in dihydrofolate reductase activity. Proc Natl Acad Sci U S A 77: 4216-4220.
-
(1980)
Proc Natl Acad Sci U S A
, vol.77
, pp. 4216-4220
-
-
Urlaub, G.1
Chasin, L.A.2
-
56
-
-
33644508373
-
Dihydrofolate reductase inhibitors as antibacterial agents
-
Hawser S, Lociuro S, Islam K, (2006) Dihydrofolate reductase inhibitors as antibacterial agents. Biochem Pharmacol 71: 941-948.
-
(2006)
Biochem Pharmacol
, vol.71
, pp. 941-948
-
-
Hawser, S.1
Lociuro, S.2
Islam, K.3
-
57
-
-
0028315470
-
The methotrexate story: A paradigm for development of cancer chemotherapeutic agents
-
In: Weber G, editor
-
Huennekens FM (1994) The methotrexate story: A paradigm for development of cancer chemotherapeutic agents. In: Weber G, editor. Advances in Enzyme Regulation, Vol 34. pp. 397-419.
-
(1994)
Advances in Enzyme Regulation
, vol.34
, pp. 397-419
-
-
Huennekens, F.M.1
-
58
-
-
77954406265
-
Novel somatic mutations in heterotrimeric G proteins in melanoma
-
Cardenas-Navia LI, Cruz P, Lin JC, Rosenberg SA, Samuels Y, et al. (2010) Novel somatic mutations in heterotrimeric G proteins in melanoma. Cancer Biol Ther 10: 33-37.
-
(2010)
Cancer Biol Ther
, vol.10
, pp. 33-37
-
-
Cardenas-Navia, L.I.1
Cruz, P.2
Lin, J.C.3
Rosenberg, S.A.4
Samuels, Y.5
-
59
-
-
0037322882
-
Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15
-
Senderek J, Bergmann C, Weber S, Ketelsen UP, Schorle H, et al. (2003) Mutation of the SBF2 gene, encoding a novel member of the myotubularin family, in Charcot-Marie-Tooth neuropathy type 4B2/11p15. Hum Mol Genet 12: 349-356.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 349-356
-
-
Senderek, J.1
Bergmann, C.2
Weber, S.3
Ketelsen, U.P.4
Schorle, H.5
-
60
-
-
84858221706
-
Ensembl 2012
-
Flicek P, Amode MR, Barrell D, Beal K, Brent S, et al. (2012) Ensembl 2012. Nucleic Acids Res 40: D84-D90.
-
(2012)
Nucleic Acids Res
, vol.40
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Brent, S.5
-
61
-
-
0036226603
-
BLAT - The BLAST-like alignment tool
-
Kent WJ, (2002) BLAT- The BLAST-like alignment tool. Genome Res 12: 656-664.
-
(2002)
Genome Res
, vol.12
, pp. 656-664
-
-
Kent, W.J.1
-
62
-
-
33644874573
-
The UCSC Genome Browser Database: update 2006
-
Hinrichs AS, Karolchik D, Baertsch R, Barber GP, Bejerano G, et al. (2006) The UCSC Genome Browser Database: update 2006. Nucleic Acids Res 34: D590-D598.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Hinrichs, A.S.1
Karolchik, D.2
Baertsch, R.3
Barber, G.P.4
Bejerano, G.5
-
63
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
In: S KSaM, editor, Totowa, NJ: Humana Press
-
Rozen S, Skaletsky H (2000) Primer3 on the WWW for general users and for biologist programmers. In: S KSaM, editor. Methods and Protocols: Methods in Molecular Biology. Totowa, NJ: Humana Press. pp. 365-386.
-
(2000)
Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
64
-
-
33644974019
-
A fast and flexible statistical model for large-scale population genotype data: Applications to inferring missing genotypes and haplotypic phase
-
Scheet P, Stephens M, (2006) A fast and flexible statistical model for large-scale population genotype data: Applications to inferring missing genotypes and haplotypic phase. Am J Hum Genet 78: 629-644.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 629-644
-
-
Scheet, P.1
Stephens, M.2
-
65
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
Frazer KA, Ballinger DG, Cox DR, Hinds DA, Stuve LL, 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
Hinds, D.A.4
Stuve, L.L.5
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