-
1
-
-
34250208181
-
Dynamic mutations as digital genetic modulators of brain development, function and dysfunction
-
Nithianantharajah J, Hannan AJ. Dynamic mutations as digital genetic modulators of brain development, function and dysfunction. Bioessays 2007; 29:525-535.
-
(2007)
Bioessays
, vol.29
, pp. 525-535
-
-
Nithianantharajah, J.1
Hannan, A.J.2
-
2
-
-
75149154292
-
Tandem repeat polymorphisms: Modulators of disease susceptibility and candidates for 'missing heritability'
-
Hannan AJ. Tandem repeat polymorphisms: modulators of disease susceptibility and candidates for 'missing heritability'. Trends Genet 2010; 26:59-65.
-
(2010)
Trends Genet
, vol.26
, pp. 59-65
-
-
Hannan, A.J.1
-
3
-
-
84934439952
-
Evolution of simple sequence repeats as mutable sites
-
Hannan AJ, ed Austin/New York: Landes Bioscience/Springer Science+Business Media
-
King DG. Evolution of simple sequence repeats as mutable sites. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/ Springer Science+Business Media, 2012:10-25.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 10-25
-
-
King, D.G.1
-
4
-
-
84934435193
-
Promoter microsatellites as modulators of human gene expression
-
Hannan AJ, ed Austin/New York: Landes Bioscience/Springer Science+Business Media
-
Sawaya SM, Bagshaw ATB, Buschiazzo E et al. Promoter microsatellites as modulators of human gene expression. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:41-54.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 41-54
-
-
Sawaya, S.M.1
Atb, B.2
Buschiazzo, E.3
-
5
-
-
0021707651
-
Enhanced gene expression by the poly(dT-dG) poly(dC-dA) sequence
-
Hamada H, Seidman M, Howard BH et al. Enhanced gene expression by the poly(dT-dG) poly(dC-dA) sequence. Mol Cell Biol 1984; 4:2622-2630.
-
(1984)
Mol Cell Biol
, vol.4
, pp. 2622-2630
-
-
Hamada, H.1
Seidman, M.2
Howard, B.H.3
-
6
-
-
0031081111
-
Simple sequence repeats as a source of quantitative genetic variation
-
Kashi Y, King D, Soller M. Simple sequence repeats as a source of quantitative genetic variation. Trends Genet 1997; 13:74-78.
-
(1997)
Trends Genet
, vol.13
, pp. 74-78
-
-
Kashi, Y.1
King, D.2
Soller, M.3
-
7
-
-
17844383699
-
Functional insights from the distribution and role of homopeptide repeat-containing proteins
-
Faux NG, Bottomley SP, Lesk AM et al. Functional insights from the distribution and role of homopeptide repeat-containing proteins. Genome Res 2005; 15:537-551.
-
(2005)
Genome Res
, vol.15
, pp. 537-551
-
-
Faux, N.G.1
Bottomley, S.P.2
Lesk, A.M.3
-
8
-
-
25144494777
-
Intragenic tandem repeats generate functional variability
-
Verstrepen KJ, Jansen A, Lewitter F et al. Intragenic tandem repeats generate functional variability. Nat Genet 2005; 37:986-990.
-
(2005)
Nat Genet
, vol.37
, pp. 986-990
-
-
Verstrepen, K.J.1
Jansen, A.2
Lewitter, F.3
-
9
-
-
33947322203
-
Differential regulation of the serotonin transporter gene by lithium is mediated by transcription factors, CCCTC binding protein and Y-Box binding protein 1, through the polymorphic intron 2 variable number tandem repeat
-
Roberts J, Scott AC, Howard MR et al. Differential regulation of the serotonin transporter gene by lithium is mediated by transcription factors, CCCTC binding protein and Y-Box binding protein 1, through the polymorphic intron 2 variable number tandem repeat. J Neurosci 2007; 27:2793-2801.
-
(2007)
J Neurosci
, vol.27
, pp. 2793-2801
-
-
Roberts, J.1
Scott, A.C.2
Howard, M.R.3
-
10
-
-
62149119245
-
Genome-wide analysis of histidine repeats reveals their role in the localization of human proteins to the nuclear speckles compartment
-
Salichs E, Ledda A, Mularoni L et al. Genome-wide analysis of histidine repeats reveals their role in the localization of human proteins to the nuclear speckles compartment. PloS Genet 2009; 5:e1000397.
-
(2009)
PloS Genet
, vol.5
-
-
Salichs, E.1
Ledda, A.2
Mularoni, L.3
-
11
-
-
72449129174
-
A global view of genomic information - Moving beyond the gene and the master regulator
-
Mattick JS, Taft RJ, Faulkner GJ. A global view of genomic information - moving beyond the gene and the master regulator. Trends Genet 2010; 26:21-28.
-
(2010)
Trends Genet
, vol.26
, pp. 21-28
-
-
Mattick, J.S.1
Taft, R.J.2
Faulkner, G.J.3
-
12
-
-
33646130830
-
Simple sequence repeats as advantageous mutators in evolution
-
Kashi Y, King DG. Simple sequence repeats as advantageous mutators in evolution. Trends Genet 2006; 22:253-259.
-
(2006)
Trends Genet
, vol.22
, pp. 253-259
-
-
Kashi, Y.1
King, D.G.2
-
13
-
-
54549127139
-
Comparative genomics and molecular dynamics of DNA repeats in eukaryotes
-
Richard GF, Kerrest A, Dujon B. Comparative genomics and molecular dynamics of DNA repeats in eukaryotes. Microbiol Mol Biol Rev 2008; 72:686-727.
-
(2008)
Microbiol Mol Biol Rev
, vol.72
, pp. 686-727
-
-
Richard, G.F.1
Kerrest, A.2
Dujon, B.3
-
14
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad DF, Pinto D, Redon R et al. Origins and functional impact of copy number variation in the human genome. Nature 2010; 464:704-712.
-
(2010)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
-
15
-
-
0035475642
-
Dynamic mutations: A decade of unstable expanded repeats in human genetic disease
-
Richards RI. Dynamic mutations: a decade of unstable expanded repeats in human genetic disease. Hum Mol Genet 2001; 10:2187-2194.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2187-2194
-
-
Richards, R.I.1
-
16
-
-
45849092558
-
Simple sequence repeats: Genetic modulators of brain function and behavior
-
Fondon JW III, Hammock EA, Hannan AJ et al. Simple sequence repeats: genetic modulators of brain function and behavior. Trends Neurosci 2008; 31:328-334.
-
(2008)
Trends Neurosci
, vol.31
, pp. 328-334
-
-
Fondon III, J.W.1
Hammock, E.A.2
Hannan, A.J.3
-
17
-
-
46449113997
-
The biological effects of simple tandem repeats: Lessons from the repeat expansion diseases
-
Usdin K. The biological effects of simple tandem repeats: lessons from the repeat expansion diseases. Genome Res 2008; 18:1011-1019.
-
(2008)
Genome Res
, vol.18
, pp. 1011-1019
-
-
Usdin, K.1
-
19
-
-
69949170793
-
The pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies
-
Bauer PO, Nukina N. The pathogenic mechanisms of polyglutamine diseases and current therapeutic strategies. J Neurochem 2009; 110:1737-1765.
-
(2009)
J Neurochem
, vol.110
, pp. 1737-1765
-
-
Bauer, P.O.1
Nukina, N.2
-
20
-
-
84934444551
-
Polyglutamine aggregation in huntington and related diseases
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/Springer Science+Business Media
-
Polling S, Hill AF, Hatters DM. Polyglutamine aggregation in Huntington and related diseases. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:125-140.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 125-140
-
-
Polling, S.1
Hill, A.F.2
Hatters, D.M.3
-
22
-
-
33745545413
-
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8
-
Moseley ML, Zu T, Ikeda Y et al. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8. Nat Genet 2006; 38:758-769.
-
(2006)
Nat Genet
, vol.38
, pp. 758-769
-
-
Moseley, M.L.1
Zu, T.2
Ikeda, Y.3
-
23
-
-
79955660764
-
An antisense CAG repeat transcript at JPH3 locus mediates expanded polyglutamine protein toxicity in Huntington's disease-like 2 mice
-
Wilburn B, Rudnicki DD, Zhao J et al. An antisense CAG repeat transcript at JPH3 locus mediates expanded polyglutamine protein toxicity in Huntington's disease-like 2 mice. Neuron 2011; 70:427-440.
-
(2011)
Neuron
, vol.70
, pp. 427-440
-
-
Wilburn, B.1
Rudnicki, D.D.2
Zhao, J.3
-
24
-
-
84934434205
-
Selective neurodegeneration, neuropathology and symptom profiles in Huntington's disease
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/Springer Science+Business Media
-
Waldvogel H, Thu D, Hogg V et al. Selective neurodegeneration, neuropathology and symptom profiles in Huntington's disease. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:141-152.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 141-152
-
-
Waldvogel, H.1
Thu, D.2
Hogg, V.3
-
25
-
-
77955643169
-
Molecular mechanisms and potential therapeutical targets in Huntington's disease
-
Zuccato C, Valenza M, Cattaneo E. Molecular mechanisms and potential therapeutical targets in Huntington's disease. Physiol Rev 2010; 90:905-981.
-
(2010)
Physiol Rev
, vol.90
, pp. 905-981
-
-
Zuccato, C.1
Valenza, M.2
Cattaneo, E.3
-
26
-
-
81255149512
-
Pathophysiology of Huntington's disease: Time-dependent alterations in synaptic and receptor function
-
Raymond LA, Andre VM, Cepeda C et al. Pathophysiology of Huntington's disease: time-dependent alterations in synaptic and receptor function. Neuroscience. 2011; 198:252-273.
-
(2011)
Neuroscience
, vol.198
, pp. 252-273
-
-
Raymond, L.A.1
Andre, V.M.2
Cepeda, C.3
-
27
-
-
78650031174
-
Huntington's disease: From molecular pathogenesis to clinical treatment
-
Ross CA, Tabrizi SJ. Huntington's disease: from molecular pathogenesis to clinical treatment. Lancet Neurol 2011; 10:83-98.
-
(2011)
Lancet Neurol
, vol.10
, pp. 83-98
-
-
Ross, C.A.1
Tabrizi, S.J.2
-
28
-
-
84934441995
-
Kennedy's disease: Clinical significance of tandem repeats in the androgen receptor
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/Springer Science+Business Media
-
Zajac JD, Fui MNT. Kennedy's disease: clinical significance of tandem repeats in the androgen receptor. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:153-168.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 153-168
-
-
Zajac, J.D.1
Fui, M.N.T.2
-
29
-
-
78651105614
-
Non-ATG-initiated translation directed by microsatellite expansions
-
Zu T, Gibbens B, Doty NS et al. Non-ATG-initiated translation directed by microsatellite expansions. Proc Natl Acad Sci USA 2011; 108:260-265.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 260-265
-
-
Zu, T.1
Gibbens, B.2
Doty, N.S.3
-
30
-
-
79953745706
-
Repeat associated non-ATG translation initiation: One DNA, two transcripts, seven reading frames, potentially nine toxic entities!
-
Pearson CE. Repeat associated non-ATG translation initiation: one DNA, two transcripts, seven reading frames, potentially nine toxic entities! PLoS Genet 2011; 7(3):e1002018.
-
(2011)
PLoS Genet
, vol.7
, Issue.3
-
-
Pearson, C.E.1
-
31
-
-
67349104211
-
Molecular mechanisms underlying polyalanine diseases
-
Messaed C, Rouleau GA. Molecular mechanisms underlying polyalanine diseases. Neurobiol Dis 2009; 34:397-405.
-
(2009)
Neurobiol Dis
, vol.34
, pp. 397-405
-
-
Messaed, C.1
Rouleau, G.A.2
-
32
-
-
84934435674
-
Polyalanine tract disorders and neurocognitive phenotypes
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/Springer Science+Business Media
-
Shoubridge C, Gecz J. Polyalanine tract disorders and neurocognitive phenotypes. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:185-204.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 185-204
-
-
Shoubridge, C.1
Gecz, J.2
-
33
-
-
59849089676
-
Microsatellite repeat instability and neurological disease
-
Brouwer JR, Willemsen R, Oostra BA. Microsatellite repeat instability and neurological disease. Bioessays 2009; 31:71-83.
-
(2009)
Bioessays
, vol.31
, pp. 71-83
-
-
Brouwer, J.R.1
Willemsen, R.2
Oostra, B.A.3
-
34
-
-
65549101751
-
Chromatin remodeling in the noncoding repeat expansion diseases
-
Kumari D, Usdin K. Chromatin remodeling in the noncoding repeat expansion diseases. J Biol Chem 2009; 284:7413-7417.
-
(2009)
J Biol Chem
, vol.284
, pp. 7413-7417
-
-
Kumari, D.1
Usdin, K.2
-
35
-
-
77953902544
-
Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approaches
-
Schmucker S, Puccio H. Understanding the molecular mechanisms of Friedreich's ataxia to develop therapeutic approaches. Hum Mol Genet 2010; 19:R103-R110.
-
(2010)
Hum Mol Genet
, vol.19
-
-
Schmucker, S.1
Puccio, H.2
-
36
-
-
84934443796
-
Unstable mutations in the FMR1 gene and the phenotypes
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/ SpringerScience+Business Media
-
Loesch D, Hagerman R. Unstable mutations in the FMR1 gene and the phenotypes. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:78-114.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 78-114
-
-
Loesch, D.1
Hagerman, R.2
-
37
-
-
84934442223
-
Characterising the neuropathology and neurobehavioural phenotype in friedreich ataxia: A systematic review
-
Hannan AJ, ed. Austin/New York: Landes Bioscience/ Springer Science+Business Media
-
Corben LA, Georgiou-Karistianis N, Bradshaw JL. Characterising the neuropathology and neurobehavioural phenotype in Friedreich ataxia: A systematic review. In: Hannan AJ, ed. Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease. Austin/New York: Landes Bioscience/Springer Science+Business Media, 2012:169-184.
-
(2012)
Tandem Repeat Polymorphisms: Genetic Plasticity, Neural Diversity and Disease
, pp. 169-184
-
-
Corben, L.A.1
Georgiou-Karistianis, N.2
Bradshaw, J.L.3
-
38
-
-
77953536158
-
Roles of trinucleotide-repeat RNA in neurological disease and degeneration
-
Li LB, Bonini NM. Roles of trinucleotide-repeat RNA in neurological disease and degeneration. Trends Neurosci 2010; 33:292-298.
-
(2010)
Trends Neurosci
, vol.33
, pp. 292-298
-
-
Li, L.B.1
Bonini, N.M.2
-
39
-
-
77952889125
-
Epigenetic changes and noncoding expanded repeats
-
Nakamori M, Thornton C. Epigenetic changes and noncoding expanded repeats. Neurobiol Dis 2010; 39:21-27.
-
(2010)
Neurobiol Dis
, vol.39
, pp. 21-27
-
-
Nakamori, M.1
Thornton, C.2
-
40
-
-
77950529265
-
RNA-mediated neurodegeneration in repeat expansion disorders
-
Todd PK, Paulson HL. RNA-mediated neurodegeneration in repeat expansion disorders. Ann Neurol 2010; 67:291-300.
-
(2010)
Ann Neurol
, vol.67
, pp. 291-300
-
-
Todd, P.K.1
Paulson, H.L.2
-
41
-
-
11144230088
-
Molecular origins of rapid and continuous morphological evolution
-
Fondon JW III, Garner HR. Molecular origins of rapid and continuous morphological evolution. Proc Natl Acad Sci USA 2004; 101:18058-18063.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 18058-18063
-
-
Fondon III, J.W.1
Garner, H.R.2
-
42
-
-
23444458415
-
Transcriptional activation modulated by homopolymeric glutamine and proline stretches
-
Gerber HP, Seipel K, Georgiev O et al. Transcriptional activation modulated by homopolymeric glutamine and proline stretches. Science 1994; 263:808-881.
-
(1994)
Science
, vol.263
, pp. 808-881
-
-
Gerber, H.P.1
Seipel, K.2
Georgiev, O.3
-
43
-
-
34347379533
-
RCPdb: An evolutionary classification and codon usage database for repeat-containing proteins
-
Faux NG, Huttley GA, Mahmood K et al. RCPdb: An evolutionary classification and codon usage database for repeat-containing proteins. Genome Res. 2007; 17:1118-1127.
-
(2007)
Genome Res
, vol.17
, pp. 1118-1127
-
-
Faux, N.G.1
Huttley, G.A.2
Mahmood, K.3
-
45
-
-
56949108250
-
Embryonic nervous system genes predominate in searches for dinucleotide simple sequence repeats flanked by conserved sequences
-
Riley DE, Krieger JN. Embryonic nervous system genes predominate in searches for dinucleotide simple sequence repeats flanked by conserved sequences. Gene 2009; 429:74-79.
-
(2009)
Gene
, vol.429
, pp. 74-79
-
-
Riley, D.E.1
Krieger, J.N.2
-
46
-
-
20644472668
-
Microsatellite instability generates diversity in brain and sociobehavioral traits
-
Hammock EAD, Young LJ. Microsatellite instability generates diversity in brain and sociobehavioral traits. Science 2005; 308:1630-1634.
-
(2005)
Science
, vol.308
, pp. 1630-1634
-
-
Ead, H.1
Young, L.J.2
-
47
-
-
0033614763
-
Microsatellite and trinucleotide-repeat evolution: Evidence for mutational bias and different rates of evolution in different lineages
-
Rubinsztein DC, Amos B, Cooper G. Microsatellite and trinucleotide-repeat evolution: evidence for mutational bias and different rates of evolution in different lineages. Philos Trans R Soc Lond B Biol Sci 1999; 354:1095-1099.
-
(1999)
Philos Trans R Soc Lond B Biol Sci
, vol.354
, pp. 1095-1099
-
-
Rubinsztein, D.C.1
Amos, B.2
Cooper, G.3
-
48
-
-
84993912315
-
Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue
-
Zeitlin S, Liu JP, Chapman DL et al. Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologue. Nat Genet 1995; 11:155-163.
-
(1995)
Nat Genet
, vol.11
, pp. 155-163
-
-
Zeitlin, S.1
Liu, J.P.2
Chapman, D.L.3
-
49
-
-
0033757718
-
Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
-
Dragatsis I, Levine MS, Zeitlin S. Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice. Nat Genet 2000; 26:300-306.
-
(2000)
Nat Genet
, vol.26
, pp. 300-306
-
-
Dragatsis, I.1
Levine, M.S.2
Zeitlin, S.3
-
50
-
-
77649219699
-
Deletion of the huntingtin polyglutamine stretch enhances neuronal autophagy and longevity in mice
-
Zheng S, Clabough EB, Sarkar S et al. Deletion of the huntingtin polyglutamine stretch enhances neuronal autophagy and longevity in mice. PLoS Genet 2010; 6(2):e1000838.
-
(2010)
PLoS Genet
, vol.6
, Issue.2
-
-
Zheng, S.1
Clabough, E.B.2
Sarkar, S.3
-
51
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ et al. Finding the missing heritability of complex diseases. Nature 2009; 461:747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
-
52
-
-
77956788631
-
Towards a complete resolution of the genetic architecture of disease
-
Singleton AB, Hardy J, Traynor BJ et al. Towards a complete resolution of the genetic architecture of disease. Trends Genet 2011; 26:438-442.
-
(2011)
Trends Genet
, vol.26
, pp. 438-442
-
-
Singleton, A.B.1
Hardy, J.2
Traynor, B.J.3
-
53
-
-
77956155218
-
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
-
Elden AC, Kim HJ, Hart MP et al. Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature 2010; 466:1069-1075.
-
(2010)
Nature
, vol.466
, pp. 1069-1075
-
-
Elden, A.C.1
Kim, H.J.2
Hart, M.P.3
-
54
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-Linked FTD and ALS
-
Dejesus-Hernandez M, Mackenzie IR, Boeve BF et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-Linked FTD and ALS. Neuron 2011; 72:245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
Dejesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
-
55
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton AE, Majounie E, Waite A et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011; 72:257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
-
57
-
-
37449023721
-
Trinucleotide repeats are prevalent among cancer-related genes
-
Haberman Y, Amariglio N, Rechavi G et al. Trinucleotide repeats are prevalent among cancer-related genes. Trends Genet 2008; 24:14-18.
-
(2008)
Trends Genet
, vol.24
, pp. 14-18
-
-
Haberman, Y.1
Amariglio, N.2
Rechavi, G.3
-
58
-
-
66349113764
-
Unstable tandem repeats in promoters confer transcriptional evolvability
-
Vinces MD, Legendre M, Caldara M et al. Unstable tandem repeats in promoters confer transcriptional evolvability. Science 2009; 324:1213-1216.
-
(2009)
Science
, vol.324
, pp. 1213-1216
-
-
Vinces, M.D.1
Legendre, M.2
Caldara, M.3
-
59
-
-
78149432728
-
Variable tandem repeats accelerate evolution of coding and regulatory sequences
-
Gemayel R, Vinces MD, Legendre M et al. Variable tandem repeats accelerate evolution of coding and regulatory sequences. Annu Rev Genet 2010; 44:445-477.
-
(2010)
Annu Rev Genet
, vol.44
, pp. 445-477
-
-
Gemayel, R.1
Vinces, M.D.2
Legendre, M.3
-
60
-
-
76549135113
-
Evolution in health and medicine Sackler colloquium: Stochastic epigenetic variation as a driving force of development, evolutionary adaptation and disease
-
Feinberg AP, Irizarry RA. Evolution in health and medicine Sackler colloquium: Stochastic epigenetic variation as a driving force of development, evolutionary adaptation and disease. Proc Natl Acad Sci USA 2010; 107 Suppl 1:1757-1764.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, Issue.SUPPL. 1
, pp. 1757-1764
-
-
Feinberg, A.P.1
Irizarry, R.A.2
-
61
-
-
42949131582
-
Marked variation in predicted and observed variability of tandem repeat loci across the human genome
-
O'Dushlaine CT, Shields DC. Marked variation in predicted and observed variability of tandem repeat loci across the human genome. BMC Genomics 2008; 9:175.
-
(2008)
BMC Genomics
, vol.9
, pp. 175
-
-
O'Dushlaine, C.T.1
Shields, D.C.2
-
62
-
-
79952202194
-
TRPing up the genome: Tandem repeat polymorphisms as dynamic sources of genetic variability in health and disease
-
Hannan AJ. TRPing up the genome: Tandem repeat polymorphisms as dynamic sources of genetic variability in health and disease. Discov Med 2010; 10:314-321.
-
(2010)
Discov Med
, vol.10
, pp. 314-321
-
-
Hannan, A.J.1
-
63
-
-
81855178276
-
Somatic retrotransposition alters the genetic landscape of the human brain
-
Baillie JK, Barnett MW, Upton KR et al. Somatic retrotransposition alters the genetic landscape of the human brain. Nature 2011; 479:534-537.
-
(2011)
Nature
, vol.479
, pp. 534-537
-
-
Baillie, J.K.1
Barnett, M.W.2
Upton, K.R.3
|