-
1
-
-
33645508511
-
Regions of extreme synonymous codon selection in mammalian genes
-
Schattner P, Diekhans M. Regions of extreme synonymous codon selection in mammalian genes. Nucl Acids Res 2006; 34: 1700-10.
-
(2006)
Nucl Acids Res
, vol.34
, pp. 1700-1710
-
-
Schattner, P.1
Diekhans, M.2
-
2
-
-
31144465926
-
Hearing silence: Non-neutral evolution at synonymous sites in mammals
-
Chamary JV, Parmley JL, Hurst LD. Hearing silence: non-neutral evolution at synonymous sites in mammals. Nature Revs Genet 2006; 7: 98-108.
-
(2006)
Nature Revs Genet
, vol.7
, pp. 98-108
-
-
Chamary, J.V.1
Parmley, J.L.2
Hurst, L.D.3
-
3
-
-
33846990531
-
Splicing and the evolution of proteins in mammals
-
Parmley JL, Urrutia AO, Potrzebowski L, Kaessmann H, Hurst LD. Splicing and the evolution of proteins in mammals. PLoS Biol 2007; 5: e14. doi: 10.1371/journal.pbio.0050014.
-
(2007)
PLoS Biol
, vol.5
, pp. e14
-
-
Parmley, J.L.1
Urrutia, A.O.2
Potrzebowski, L.3
Kaessmann, H.4
Hurst, L.D.5
-
4
-
-
34250212837
-
How do synonymous mutations affect fitness?
-
Parmley JL, Hurst LD. How do synonymous mutations affect fitness? BioEssays 2007; 29: 515-9.
-
(2007)
BioEssays
, vol.29
, pp. 515-519
-
-
Parmley, J.L.1
Hurst, L.D.2
-
5
-
-
78650304100
-
Synonymous but not the same: The causes and consequences of codon bias
-
Plotkin JB, Kudla G. Synonymous but not the same: the causes and consequences of codon bias. Nature Revs Genet 2011; 12: 32-42.
-
(2011)
Nature Revs Genet
, vol.12
, pp. 32-42
-
-
Plotkin, J.B.1
Kudla, G.2
-
6
-
-
0019474499
-
Correlation between the abundance of Escherichia coli transfer RNAs and the occurence of the respective codons in its protein genes
-
Ikemura T. Correlation between the abundance of Escherichia coli transfer RNAs and the occurence of the respective codons in its protein genes. J Mol Biol 1981; 146: 1-21.
-
(1981)
J Mol Biol
, vol.146
, pp. 1-21
-
-
Ikemura, T.1
-
7
-
-
13444291526
-
Codon bias as a factor in regulating expression via translation rate in the human genome
-
Lavner Y, Kotlar D. Codon bias as a factor in regulating expression via translation rate in the human genome. Gene 2005; 345: 127-38.
-
(2005)
Gene
, vol.345
, pp. 127-138
-
-
Lavner, Y.1
Kotlar, D.2
-
8
-
-
3843068862
-
Selective and mutational patterns associated with gene expression in humans: Influences on synonymous composition and intron presence
-
Comeron JM. Selective and mutational patterns associated with gene expression in humans: influences on synonymous composition and intron presence. Genetics 2004; 167: 1293-304.
-
(2004)
Genetics
, vol.167
, pp. 1293-1304
-
-
Comeron, J.M.1
-
9
-
-
77956521917
-
Silent mutations in sight: Co-variations in tRNA abundance as a key to unravel consequences of silent mutations
-
Czech A, Fedyunin I, Zhang G, Ignatova Z. Silent mutations in sight: co-variations in tRNA abundance as a key to unravel consequences of silent mutations. Mol Biosyst 2010; 10: 1767-72.
-
(2010)
Mol Biosyst
, vol.10
, pp. 1767-1772
-
-
Czech, A.1
Fedyunin, I.2
Zhang, G.3
Ignatova, Z.4
-
10
-
-
48249093081
-
Heterologous protein expression is enhanced by harmonizing the codon usage frequencies of the target gene with those of the expression host
-
Angov E, Hillier CJ, Kincaid RL, Lyon JA. Heterologous protein expression is enhanced by harmonizing the codon usage frequencies of the target gene with those of the expression host. PLoS One 2008; 3(5): e2189. doi: 10.1371/journal.pone.0002189.
-
(2008)
PLoS One
, vol.3
, Issue.5
, pp. e2189
-
-
Angov, E.1
Hillier, C.J.2
Kincaid, R.L.3
Lyon, J.A.4
-
11
-
-
46449120581
-
Virus attenuation by genome-scale changes in codon pair bias
-
Coleman JR, Papamichail D, Skiena S, Futcher B, Wimmer E, Mueller S. Virus attenuation by genome-scale changes in codon pair bias. Science 2008; 320: 1784-7.
-
(2008)
Science
, vol.320
, pp. 1784-1787
-
-
Coleman, J.R.1
Papamichail, D.2
Skiena, S.3
Futcher, B.4
Wimmer, E.5
Mueller, S.6
-
12
-
-
0023650543
-
The Codon Adaptation Index-a measure of directional synonymous codon usage bias, and its potential applications
-
Sharp PM, Li WH. The Codon Adaptation Index-a measure of directional synonymous codon usage bias, and its potential applications. Nucl Acids Res 1987; 15: 1281-95.
-
(1987)
Nucl Acids Res
, vol.15
, pp. 1281-1295
-
-
Sharp, P.M.1
Li, W.H.2
-
13
-
-
18144386947
-
Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution
-
Pagani F, Raponi M, Baralle FE. Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution. Proc Natl Acad Sci USA 2005; 102: 6368-72.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 6368-6372
-
-
Pagani, F.1
Raponi, M.2
Baralle, F.E.3
-
14
-
-
0036207384
-
Listening to silence and understanding nonsense: Exonic mutations that affect splicing
-
Cartegni L, Chew SL, Krainer AR. Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nature Revs Genet 2002; 3: 285-98.
-
(2002)
Nature Revs Genet
, vol.3
, pp. 285-298
-
-
Cartegni, L.1
Chew, S.L.2
Krainer, A.R.3
-
15
-
-
12744272023
-
Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1
-
Amati-Bonneau P, Pasquier L, Lainey E, Ferre M, Odent S, Malthiery Y, Bonneau D, Reynier P. Sporadic optic atrophy due to synonymous codon change altering mRNA splicing of OPA1. Clin Genet 2005; 67: 102-3.
-
(2005)
Clin Genet
, vol.67
, pp. 102-103
-
-
Amati-Bonneau, P.1
Pasquier, L.2
Lainey, E.3
Ferre, M.4
Odent, S.5
Malthiery, Y.6
Bonneau, D.7
Reynier, P.8
-
16
-
-
0345659221
-
Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease
-
Fernandez-Cadenas I, Andreu AL, Gamez J, Gonzalo R, Martin MA, Rubio JC, Arenas J. Splicing mosaic of the myophosphorylase gene due to a silent mutation in McArdle disease. Neurology 2003; 61: 1432-4.
-
(2003)
Neurology
, vol.61
, pp. 1432-1434
-
-
Fernandez-Cadenas, I.1
Andreu, A.L.2
Gamez, J.3
Gonzalo, R.4
Martin, M.A.5
Rubio, J.C.6
Arenas, J.7
-
17
-
-
0031745172
-
A silent mutation, C924T (G308G), in the L1CAM gene results in X linked hydrocephalus (HSAS)
-
Du YZ, Dickerson C, Aylsworth AS, Schwartz CE. A silent mutation, C924T (G308G), in the L1CAM gene results in X linked hydrocephalus (HSAS). J Med Genet 1998; 35: 456-62.
-
(1998)
J Med Genet
, vol.35
, pp. 456-462
-
-
Du, Y.Z.1
Dickerson, C.2
Aylsworth, A.S.3
Schwartz, C.E.4
-
18
-
-
18844417181
-
Type i Glanzmann thrombasthenia caused by an apparently silent β 3 mutation that results in aberrant splicing and reduced β 3 mRNA
-
Xie JL, Pabon D, Jayo A, Butta N, Gonzalez-Manchon C. Type I Glanzmann thrombasthenia caused by an apparently silent β 3 mutation that results in aberrant splicing and reduced β 3 mRNA. Thromb Haemost 2005; 67: 897-903.
-
(2005)
Thromb Haemost
, vol.67
, pp. 897-903
-
-
Xie, J.L.1
Pabon, D.2
Jayo, A.3
Butta, N.4
Gonzalez-Manchon, C.5
-
19
-
-
17644409768
-
Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation
-
Flusser H, Korman SH, Sato K, Matsubara Y, Galil A, Kure S. Mild glycine encephalopathy (NKH) in a large kindred due to a silent exonic GLDC splice mutation. Neurology 2005; 64: 1426-30.
-
(2005)
Neurology
, vol.64
, pp. 1426-1430
-
-
Flusser, H.1
Korman, S.H.2
Sato, K.3
Matsubara, Y.4
Galil, A.5
Kure, S.6
-
20
-
-
2442532778
-
Severe subacute GM2 gangliosidosis caused by an apparently silent HEXA mutation (V324V) that results in aberrant splicing and reduced HEXA mRNA
-
Wicklow BA, Ivanovich JL, Plews MM, Salo TJ, Noetzel MJ, Lueder GT, Cartegni L, Kaback MM, Sandhoff K, Steiner RD, Triggs-Raine BL. Severe subacute GM2 gangliosidosis caused by an apparently silent HEXA mutation (V324V) that results in aberrant splicing and reduced HEXA mRNA. Am J Med Genet A 2004; 127A: 158-66.
-
(2004)
Am J Med Genet A
, vol.127 A
, pp. 158-166
-
-
Wicklow, B.A.1
Ivanovich, J.L.2
Plews, M.M.3
Salo, T.J.4
Noetzel, M.J.5
Lueder, G.T.6
Cartegni, L.7
Kaback, M.M.8
Sandhoff, K.9
Steiner, R.D.10
Triggs-Raine, B.L.11
-
21
-
-
0031202066
-
Silent mutation induces exon skipping of fibrilin-1 gene in Marfan syndrome
-
Liu W, Quian C, Francke U. Silent mutation induces exon skipping of fibrilin-1 gene in Marfan syndrome. Nat Genet 1997; 16: 328-9.
-
(1997)
Nat Genet
, vol.16
, pp. 328-329
-
-
Liu, W.1
Quian, C.2
Francke, U.3
-
22
-
-
0035122522
-
A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria
-
Chao HK, Hsiao KJ, Su TS. A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuria. Hum Genet 2001; 108: 14-9.
-
(2001)
Hum Genet
, vol.108
, pp. 14-19
-
-
Chao, H.K.1
Hsiao, K.J.2
Su, T.S.3
-
23
-
-
0036534129
-
Alternative splicing: Multiple control mechanisms and involvement in human disease
-
Caceres JF, Komblihtt AR. Alternative splicing: multiple control mechanisms and involvement in human disease. Trends Genet 2002; 18: 186-93.
-
(2002)
Trends Genet
, vol.18
, pp. 186-193
-
-
Caceres, J.F.1
Komblihtt, A.R.2
-
24
-
-
17644370601
-
Biased codon usage near intron-exon junctions: Selection on splicing enhancers splice-site recognition or something else?
-
Chamary JV, Hurst LD. Biased codon usage near intron-exon junctions: selection on splicing enhancers, splice-site recognition or something else? Trends Genet 2005; 21: 256-9.
-
(2005)
Trends Genet
, vol.21
, pp. 256-259
-
-
Chamary, J.V.1
Hurst, L.D.2
-
25
-
-
64849114915
-
Coding-sequence determinants of gene expression in Escherichia coli
-
Kudla G, Murray AW, Tollervey D, Plotkin JB. Coding-sequence determinants of gene expression in Escherichia coli. Science 2009; 324: 255-8.
-
(2009)
Science
, vol.324
, pp. 255-258
-
-
Kudla, G.1
Murray, A.W.2
Tollervey, D.3
Plotkin, J.B.4
-
26
-
-
70349199628
-
Design parameters to control synthetic gene expression in Escherichia coli
-
Welch M, Govindarajan S, Nees JE, Villalobos A, Gurney A, Minshull J, Gustafsson C. Design parameters to control synthetic gene expression in Escherichia coli. PLoS One 2009; 4: e7002. doi: 10.1371/journal.pone.0007002.
-
(2009)
PLoS One
, vol.4
, pp. e7002
-
-
Welch, M.1
Govindarajan, S.2
Nees, J.E.3
Villalobos, A.4
Gurney, A.5
Minshull, J.6
Gustafsson, C.7
-
27
-
-
0025166089
-
Secondary structure of the ribosomal binding site determines translational efficiency: A quantitative analysis
-
De Smit MH, van Duin J. Secondary structure of the ribosomal binding site determines translational efficiency: a quantitative analysis. Proc Natl Acad Sci USA 1990; 87: 7668-72.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 7668-7672
-
-
De Smit, M.H.1
Van Duin, J.2
-
28
-
-
78650477258
-
Tuning protein expression using synonymous codon libraries targeted to the 5mRNA coding region
-
Goltermann L, Borch Jensen M, Bentin T. Tuning protein expression using synonymous codon libraries targeted to the 5mRNA coding region. Protein Eng Des Sel 2011; 24: 123-9.
-
(2011)
Protein Eng des Sel
, vol.24
, pp. 123-129
-
-
Goltermann, L.1
Borch Jensen, M.2
Bentin, T.3
-
29
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
Nackley AG, Shabalina SA, Tchivileva IE, Satterfield K, Korchynskyi O, Makarov SS, Maixner W, Diatchenko L. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006; 314: 1930-3.
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
Satterfield, K.4
Korchynskyi, O.5
Makarov, S.S.6
Maixner, W.7
Diatchenko, L.8
-
30
-
-
80051713330
-
Disruptive mRNA folding increases translational efficiency of catechol-O-methyltransferase variant
-
Tsao D, Shabalina SA, Gauthier J, Dokholyan NV, Diatchenko L. Disruptive mRNA folding increases translational efficiency of catechol-O-methyltransferase variant. Nucleic Acids Res 2011; 39: 6201-12.
-
(2011)
Nucleic Acids Res
, vol.39
, pp. 6201-6212
-
-
Tsao, D.1
Shabalina, S.A.2
Gauthier, J.3
Dokholyan, N.V.4
Diatchenko, L.5
-
31
-
-
77956537712
-
A synonymous nucleotide polymorphism in A F508 CFTR alters the secondary structure of the mRNA and the expression of the mutant protein
-
Bartoszewski RA, Jablonsky M, Bartoszewska S, Stevenson L, Dai Q, Kappes J, Collawn JF, Bebok Z. A synonymous nucleotide polymorphism in A F508 CFTR alters the secondary structure of the mRNA and the expression of the mutant protein. J Biol Chem 2010; 285: 28741-8.
-
(2010)
J Biol Chem
, vol.285
, pp. 28741-28748
-
-
Bartoszewski, R.A.1
Jablonsky, M.2
Bartoszewska, S.3
Stevenson, L.4
Dai, Q.5
Kappes, J.6
Collawn, J.F.7
Bebok, Z.8
-
32
-
-
0037320652
-
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
-
Duan J, Wainwright MS, Comeron JM, Saitou N, Sanders AR, Gelernter J, Gejman PV. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Human Mol Genet 2003; 12: 205-16.
-
(2003)
Human Mol Genet
, vol.12
, pp. 205-216
-
-
Duan, J.1
Wainwright, M.S.2
Comeron, J.M.3
Saitou, N.4
Sanders, A.R.5
Gelernter, J.6
Gejman, P.V.7
-
33
-
-
0346104825
-
Mammalian mutation pressure, synonymous codon choice and mRNA degradation
-
Duan J, Antezana MA. Mammalian mutation pressure, synonymous codon choice and mRNA degradation. J Mol Evol 2003; 57: 694-701.
-
(2003)
J Mol Evol
, vol.57
, pp. 694-701
-
-
Duan, J.1
Antezana, M.A.2
-
34
-
-
30744432134
-
Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals
-
Chamary JV, Hurst LD. Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals. Genome Biol 2005; 6: R75. doi: 10.1186/gb-2005-6-9-r75.
-
(2005)
Genome Biol
, vol.6
, pp. R75
-
-
Chamary, J.V.1
Hurst, L.D.2
-
35
-
-
19544391975
-
A synonymous SNP of the corneodesmin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups
-
Capon F, Allen MH, Ameen M, Burden AD, Tillman D, Barker JN, Trembath RC. A synonymous SNP of the corneodesmin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups. Human Mol Genet 2004; 13: 2361-8.
-
(2004)
Human Mol Genet
, vol.13
, pp. 2361-2368
-
-
Capon, F.1
Allen, M.H.2
Ameen, M.3
Burden, A.D.4
Tillman, D.5
Barker, J.N.6
Trembath, R.C.7
-
36
-
-
33746435693
-
Preliminary assessment of the impact of microRNAmediated regulation on coding sequence evolution in mammals
-
Hurst LD. Preliminary assessment of the impact of microRNAmediated regulation on coding sequence evolution in mammals. J Mol Evol 2006; 63: 174-82.
-
(2006)
J Mol Evol
, vol.63
, pp. 174-182
-
-
Hurst, L.D.1
-
37
-
-
79952134938
-
A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn s disease
-
Brest P, Lapaquette P, Souidi M, Lebrigand K, Cesaro A, Vouret-Craviari V, Mari B, Barbry P, Mosnier J-F, Hebuterne X, Harel-Bellan A, Mograbi B, Darfeuille-Michaud A, Hofman P. A synonymous variant in IRGM alters a binding site for miR-196 and causes deregulation of IRGM-dependent xenophagy in Crohn s disease. Nat Genet 2011; 43: 242-6.
-
(2011)
Nat Genet
, vol.43
, pp. 242-246
-
-
Brest, P.1
Lapaquette, P.2
Souidi, M.3
Lebrigand, K.4
Cesaro, A.5
Vouret-Craviari, V.6
Mari, B.7
Barbry, P.8
Mosnier, J.-F.9
Hebuterne, X.10
Harel-Bellan, A.11
Mograbi, B.12
Darfeuille-Michaud, A.13
Hofman, P.14
-
38
-
-
34347338690
-
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn s disease susceptibility
-
Parkes M, Barrett JC, Prescott NJ, Tremeling M, Anderson CA, Fisher SA, Roberts RG, Nimmo ER, Cummings FR, Soars D, Drummond H, Lees CW, Khawaja SA, Bagnall R, Burke DA, Todhunter CE, Ahmad T, Onnie CM, McArdle W, Strachan D, Bethel G, Bryan C, Lewis CM, Deloukas P, Forbes A, Sanderson J, Jewell DP, Satsangi J, Mansfield JC, the Wellcome Trust Case Control Consortium, Cardon L, Mathew CG. Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn s disease susceptibility. Nat Genet 2007; 39: 830-2.
-
(2007)
Nat Genet
, vol.39
, pp. 830-832
-
-
Parkes, M.1
Barrett, J.C.2
Prescott, N.J.3
Tremeling, M.4
Anderson, C.A.5
Fisher, S.A.6
Roberts, R.G.7
Nimmo, E.R.8
Cummings, F.R.9
Soars, D.10
Drummond, H.11
Lees, C.W.12
Khawaja, S.A.13
Bagnall, R.14
Burke, D.A.15
Todhunter, C.E.16
Ahmad, T.17
Onnie, C.M.18
McArdle, W.19
Strachan, D.20
Bethel, G.21
Bryan, C.22
Lewis, C.M.23
Deloukas, P.24
Forbes, A.25
Sanderson, J.26
Jewell, D.P.27
Satsangi, J.28
Mansfield, J.C.29
more..
-
39
-
-
0029908504
-
Protein secondary structural types are differentially coded on messger RNA
-
Thanaraj TA, Argos P. Protein secondary structural types are differentially coded on messger RNA. Protein Sci 1996; 5: 1973-83.
-
(1996)
Protein Sci
, vol.5
, pp. 1973-1983
-
-
Thanaraj, T.A.1
Argos, P.2
-
40
-
-
0032493780
-
Specific correlations between relative synonymous codon usage and protein secondary structural units
-
Oresic M, Shalloway D. Specific correlations between relative synonymous codon usage and protein secondary structural units. J Mol Biol 1998; 281: 31-48.
-
(1998)
J Mol Biol
, vol.281
, pp. 31-48
-
-
Oresic, M.1
Shalloway, D.2
-
41
-
-
58149199728
-
A pause for thought along the co-translational folding pathway
-
Komar AA. A pause for thought along the co-translational folding pathway. Trends Biochem Sci 2008; 34: 16-24.
-
(2008)
Trends Biochem Sci
, vol.34
, pp. 16-24
-
-
Komar, A.A.1
-
42
-
-
62049083910
-
Transient ribosomal attenuation coordinates protein synthesis and co-translational folding
-
Zhang G, Hubalewska M, Ignatova Z. Transient ribosomal attenuation coordinates protein synthesis and co-translational folding. Nature Struct Mol Biol 2009; 16: 274-80.
-
(2009)
Nature Struct Mol Biol
, vol.16
, pp. 274-280
-
-
Zhang, G.1
Hubalewska, M.2
Ignatova, Z.3
-
43
-
-
79957852647
-
The imprint of codons on protein structure
-
Deane CM, Saunders R. The imprint of codons on protein structure. Biotechnol J 2011; 6: 641-9.
-
(2011)
Biotechnol J
, vol.6
, pp. 641-649
-
-
Deane, C.M.1
Saunders, R.2
-
44
-
-
79957798888
-
Codon usage: Nature s roadmap to expression and folding of proteins
-
Angov E. Codon usage: nature s roadmap to expression and folding of proteins. Biotechnol J 2011; 6: 650-9.
-
(2011)
Biotechnol J
, vol.6
, pp. 650-659
-
-
Angov, E.1
-
45
-
-
0036295371
-
Silent mutations affect in vivo protein folding in Escherichia coli
-
Cortazzo P, Cervenansky C, Marin M, Reiss C, Ehrlich R, Deana A. Silent mutations affect in vivo protein folding in Escherichia coli. Biochem Biophys Res Comm 2002; 293: 537-41.
-
(2002)
Biochem Biophys Res Comm
, vol.293
, pp. 537-541
-
-
Cortazzo, P.1
Cervenansky, C.2
Marin, M.3
Reiss, C.4
Ehrlich, R.5
Deana, A.6
-
46
-
-
33846504706
-
A silent polymorphism in the MDR1 gene changes substrate specificity
-
Kimchi-Sarfaty C, Oh JM, Kim IW, Sauna ZE, Calcagno AM, Ambudkar SV, Gottesman MM. A silent polymorphism in the MDR1 gene changes substrate specificity. Science 2007; 315: 525-8.
-
(2007)
Science
, vol.315
, pp. 525-528
-
-
Kimchi-Sarfaty, C.1
Oh, J.M.2
Kim, I.W.3
Sauna, Z.E.4
Calcagno, A.M.5
Ambudkar, S.V.6
Gottesman, M.M.7
-
47
-
-
25144433260
-
Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C δ T affects mRNA stability
-
Wang D, Johnson AD, Papp AC, Kroetz DL, Sad e e W. Multidrug resistance polypeptide 1 (MDR1, ABCB1) variant 3435C δ T affects mRNA stability. Pharmacogen Genom 2005; 15: 693-704.
-
(2005)
Pharmacogen Genom
, vol.15
, pp. 693-704
-
-
Wang, D.1
Johnson, A.D.2
Papp, A.C.3
Kroetz, D.L.4
Sadee, W.5
-
48
-
-
64649101364
-
A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function
-
Fung KL, Gottesman MM. A synonymous polymorphism in a common MDR1 (ABCB1) haplotype shapes protein function. Biochim Biophys Acta 2009; 1794: 860-71.
-
(2009)
Biochim Biophys Acta
, vol.1794
, pp. 860-871
-
-
Fung, K.L.1
Gottesman, M.M.2
-
49
-
-
35448992847
-
Silent polymorphisms speak: How they affect pharmacogenomics and the treatment of cancer
-
Sauna ZE, Kimchi-Sarfaty C, Ambudkar SV, Gottesman MM. Silent polymorphisms speak: how they affect pharmacogenomics and the treatment of cancer. Cancer Res 2007; 67: 9609-12.
-
(2007)
Cancer Res
, vol.67
, pp. 9609-9612
-
-
Sauna, Z.E.1
Kimchi-Sarfaty, C.2
Ambudkar, S.V.3
Gottesman, M.M.4
-
50
-
-
73449145712
-
Silent (synonymous) SNPs: Should we care about them?
-
Hunt R, Sauna ZE, Ambudkar SV, Gottesman MM, Kimchi-Sarfaty C. Silent (synonymous) SNPs: should we care about them? Methods Mol Biol 2009; 578: 23-39.
-
(2009)
Methods Mol Biol
, vol.578
, pp. 23-39
-
-
Hunt, R.1
Sauna, Z.E.2
Ambudkar, S.V.3
Gottesman, M.M.4
Kimchi-Sarfaty, C.5
-
51
-
-
77956663124
-
Differential arginylation of actin isoforms is regulated by coding sequence-dependent degradation
-
Zhang F, Saha S, Shabalina SA, Kashina A. Differential arginylation of actin isoforms is regulated by coding sequence-dependent degradation. Science 2010; 329: 1534-7.
-
(2010)
Science
, vol.329
, pp. 1534-1537
-
-
Zhang, F.1
Saha, S.2
Shabalina, S.A.3
Kashina, A.4
-
52
-
-
70350218734
-
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk
-
Yang R, Chen B, Hemminki K, Wappenschmidt B, Engel C, Sutter C, Ditsch N, Weber BH, Niederacher D, Arnold N, Meindl A, Bartram CR, Schmutzler RK, Burwinkel B. Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk. Breast Cancer Res Treat 2009; 118: 407-13.
-
(2009)
Breast Cancer Res Treat
, vol.118
, pp. 407-413
-
-
Yang, R.1
Chen, B.2
Hemminki, K.3
Wappenschmidt, B.4
Engel, C.5
Sutter, C.6
Ditsch, N.7
Weber, B.H.8
Niederacher, D.9
Arnold, N.10
Meindl, A.11
Bartram, C.R.12
Schmutzler, R.K.13
Burwinkel, B.14
-
53
-
-
79959829720
-
Widespread RNA and DNA sequence differences in the human transcriptome
-
Li M, Wang, IX, Li Y, Bruzel A, Richards AL, Toung JM, Cheung VG. Widespread RNA and DNA sequence differences in the human transcriptome. Science 2011; 333: 53-8.
-
(2011)
Science
, vol.333
, pp. 53-58
-
-
Li, M.1
Wang, I.X.2
Li, Y.3
Bruzel, A.4
Richards, A.L.5
Toung, J.M.6
Cheung, V.G.7
-
54
-
-
79551629027
-
Translational pausing ensures membrane targeting and cytoplasmic splicing of XBP1u mRNA
-
Yanagitani K, Kimata Y, Kadokura H, Kohno K. Translational pausing ensures membrane targeting and cytoplasmic splicing of XBP1u mRNA. Science 2011; 331: 586-9.
-
(2011)
Science
, vol.331
, pp. 586-589
-
-
Yanagitani, K.1
Kimata, Y.2
Kadokura, H.3
Kohno, K.4
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