-
1
-
-
57749195712
-
RNA-Seq: a revolutionary tool for transcriptomics
-
Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet. 2009;10(1):57-63.
-
(2009)
Nat Rev Genet
, vol.10
, Issue.1
, pp. 57-63
-
-
Wang, Z.1
Gerstein, M.2
Snyder, M.3
-
2
-
-
46249130709
-
The beginning of the end for microarrays?
-
Shendure J. The beginning of the end for microarrays? Nat Methods. 2008;5(7):585-7.
-
(2008)
Nat Methods
, vol.5
, Issue.7
, pp. 585-587
-
-
Shendure, J.1
-
3
-
-
84882692468
-
Large Scale Comparison of Gene Expression Levels by Microarrays and RNAseq Using TCGA Data
-
Guo Y, Sheng Q, Li J, Ye F, Samuels DC, Shyr Y. Large Scale Comparison of Gene Expression Levels by Microarrays and RNAseq Using TCGA Data. PLoS One. 2013;8(8):e71462.
-
(2013)
PLoS One
, vol.8
, Issue.8
, pp. e71462
-
-
Guo, Y.1
Sheng, Q.2
Li, J.3
Ye, F.4
Samuels, D.C.5
Shyr, Y.6
-
4
-
-
84889664774
-
Evaluation of read count based RNAseq analysis methods
-
Guo Y, Li CI, Ye F, Shyr Y. Evaluation of read count based RNAseq analysis methods. BMC Genomics. 2013;14 Suppl 8:S2.
-
(2013)
BMC Genomics
, vol.14
, pp. S2
-
-
Guo, Y.1
Li, C.I.2
Ye, F.3
Shyr, Y.4
-
5
-
-
74049148179
-
3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer
-
Asmann YW, Klee EW, Thompson EA, Perez EA, Middha S, Oberg AL, et al. 3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer. BMC Genomics. 2009;10:531.
-
(2009)
BMC Genomics
, vol.10
, pp. 531
-
-
Asmann, Y.W.1
Klee, E.W.2
Thompson, E.A.3
Perez, E.A.4
Middha, S.5
Oberg, A.L.6
-
6
-
-
46249103973
-
Stem cell transcriptome profiling via massive-scale mRNA sequencing
-
Cloonan N, Forrest AR, Kolle G, Gardiner BB, Faulkner GJ, Brown MK, et al. Stem cell transcriptome profiling via massive-scale mRNA sequencing. Nat Methods. 2008;5(7):613-9.
-
(2008)
Nat Methods
, vol.5
, Issue.7
, pp. 613-619
-
-
Cloonan, N.1
Forrest, A.R.2
Kolle, G.3
Gardiner, B.B.4
Faulkner, G.J.5
Brown, M.K.6
-
7
-
-
50649089207
-
RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays
-
Marioni JC, Mason CE, Mane SM, Stephens M, Gilad Y. RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. Genome Res. 2008;18(9):1509-17.
-
(2008)
Genome Res
, vol.18
, Issue.9
, pp. 1509-1517
-
-
Marioni, J.C.1
Mason, C.E.2
Mane, S.M.3
Stephens, M.4
Gilad, Y.5
-
8
-
-
84887610943
-
Beyond microRNA - Novel RNAs derived from small non-coding RNA and their implication in cancer
-
Martens-Uzunova ES, Olvedy M, Jenster G. Beyond microRNA - Novel RNAs derived from small non-coding RNA and their implication in cancer. Cancer Lett. 2013;340:201-11.
-
(2013)
Cancer Lett
, vol.340
, pp. 201-211
-
-
Martens-Uzunova, E.S.1
Olvedy, M.2
Jenster, G.3
-
9
-
-
42949132235
-
Hidden layers of human small RNAs
-
Kawaji H, Nakamura M, Takahashi Y, Sandelin A, Katayama S, Fukuda S, et al. Hidden layers of human small RNAs. BMC Genomics. 2008;9(1):157.
-
(2008)
BMC Genomics
, vol.9
, Issue.1
, pp. 157
-
-
Kawaji, H.1
Nakamura, M.2
Takahashi, Y.3
Sandelin, A.4
Katayama, S.5
Fukuda, S.6
-
10
-
-
71549169628
-
Filtering of deep sequencing data reveals the existence of abundant Dicer-dependent small RNAs derived from tRNAs
-
Cole C, Sobala A, Lu C, Thatcher SR, Bowman A, Brown JW, et al. Filtering of deep sequencing data reveals the existence of abundant Dicer-dependent small RNAs derived from tRNAs. RNA. 2009;15(12):2147-60.
-
(2009)
RNA
, vol.15
, Issue.12
, pp. 2147-2160
-
-
Cole, C.1
Sobala, A.2
Lu, C.3
Thatcher, S.R.4
Bowman, A.5
Brown, J.W.6
-
11
-
-
72749089855
-
A novel class of small RNAs: tRNA-derived RNA fragments (tRFs)
-
Lee YS, Shibata Y, Malhotra A, Dutta A. A novel class of small RNAs: tRNA-derived RNA fragments (tRFs). Genes Dev. 2009;23(22):2639-49.
-
(2009)
Genes Dev
, vol.23
, Issue.22
, pp. 2639-2649
-
-
Lee, Y.S.1
Shibata, Y.2
Malhotra, A.3
Dutta, A.4
-
12
-
-
67650604265
-
Stressing out over tRNA cleavage
-
Thompson DM, Parker R. Stressing out over tRNA cleavage. Cell. 2009;138(2):215-9.
-
(2009)
Cell
, vol.138
, Issue.2
, pp. 215-219
-
-
Thompson, D.M.1
Parker, R.2
-
13
-
-
84901945329
-
A comparison of microRNA sequencing reproducibility and noise reduction using mirVana and TRIzol isolation methods
-
Guo Y, Bosompem A, Zhong X, Clark T, Shyr Y, Kim AS. A comparison of microRNA sequencing reproducibility and noise reduction using mirVana and TRIzol isolation methods. Int J Comput Biol Drug Des. 2014;7(2-3):102-12.
-
(2014)
Int J Comput Biol Drug Des
, vol.7
, Issue.2-3
, pp. 102-112
-
-
Guo, Y.1
Bosompem, A.2
Zhong, X.3
Clark, T.4
Shyr, Y.5
Kim, A.S.6
-
14
-
-
84938562598
-
Alternative applications for distinct RNA sequencing strategies
-
Han L, Vickers KC, Samuels DC, Guo Y. Alternative applications for distinct RNA sequencing strategies. Brief Bioinform. 2014;16:629-39.
-
(2014)
Brief Bioinform
, vol.16
, pp. 629-639
-
-
Han, L.1
Vickers, K.C.2
Samuels, D.C.3
Guo, Y.4
-
15
-
-
84961290495
-
Mining diverse small RNA species in the deep transcriptome
-
Vickers KC, Roteta LA, Hucheson-Dilks H, Han L, Guo Y. Mining diverse small RNA species in the deep transcriptome. Trends Biochem Sci. 2015;40(1):4-7.
-
(2015)
Trends Biochem Sci
, vol.40
, Issue.1
, pp. 4-7
-
-
Vickers, K.C.1
Roteta, L.A.2
Hucheson-Dilks, H.3
Han, L.4
Guo, Y.5
-
16
-
-
77956278708
-
Deep sequencing of human nuclear and cytoplasmic small RNAs reveals an unexpectedly complex subcellular distribution of miRNAs and tRNA 3' trailers
-
Liao JY, Ma LM, Guo YH, Zhang YC, Zhou H, Shao P, et al. Deep sequencing of human nuclear and cytoplasmic small RNAs reveals an unexpectedly complex subcellular distribution of miRNAs and tRNA 3' trailers. PLoS One. 2010;5(5):e10563.
-
(2010)
PLoS One
, vol.5
, Issue.5
, pp. e10563
-
-
Liao, J.Y.1
Ma, L.M.2
Guo, Y.H.3
Zhang, Y.C.4
Zhou, H.5
Shao, P.6
-
17
-
-
84871586107
-
Hints of tRNA-Derived Small RNAs Role in RNA Silencing Mechanisms
-
Garcia-Silva MR, Cabrera-Cabrera F, Guida MC, Cayota A. Hints of tRNA-Derived Small RNAs Role in RNA Silencing Mechanisms. Genes (Basel). 2012;3(4):603-14.
-
(2012)
Genes (Basel)
, vol.3
, Issue.4
, pp. 603-614
-
-
Garcia-Silva, M.R.1
Cabrera-Cabrera, F.2
Guida, M.C.3
Cayota, A.4
-
18
-
-
58149498297
-
Stress induces tRNA cleavage by angiogenin in mammalian cells
-
Fu H, Feng J, Liu Q, Sun F, Tie Y, Zhu J, et al. Stress induces tRNA cleavage by angiogenin in mammalian cells. FEBS Lett. 2009;583(2):437-42.
-
(2009)
FEBS Lett
, vol.583
, Issue.2
, pp. 437-442
-
-
Fu, H.1
Feng, J.2
Liu, Q.3
Sun, F.4
Tie, Y.5
Zhu, J.6
-
19
-
-
0016838773
-
Specific cleavage of tRNA by nuclease S1
-
Harada F, Dahlberg JE. Specific cleavage of tRNA by nuclease S1. Nucleic Acids Res. 1975;2(6):865-71.
-
(1975)
Nucleic Acids Res
, vol.2
, Issue.6
, pp. 865-871
-
-
Harada, F.1
Dahlberg, J.E.2
-
20
-
-
84924990215
-
The importance of being modified: an unrealized code to RNA structure and function
-
Agris PF. The importance of being modified: an unrealized code to RNA structure and function. RNA. 2015;21(4):552-4.
-
(2015)
RNA
, vol.21
, Issue.4
, pp. 552-554
-
-
Agris, P.F.1
-
21
-
-
0027433143
-
A primer extension assay for modification of guanine by Ni(II) complexes
-
Woodson SA, Muller JG, Burrows CJ, Rokita SE. A primer extension assay for modification of guanine by Ni(II) complexes. Nucleic Acids Res. 1993;21(23):5524-5.
-
(1993)
Nucleic Acids Res
, vol.21
, Issue.23
, pp. 5524-5525
-
-
Woodson, S.A.1
Muller, J.G.2
Burrows, C.J.3
Rokita, S.E.4
-
22
-
-
84888418863
-
HAMR: high-throughput annotation of modified ribonucleotides
-
Ryvkin P, Leung YY, Silverman IM, Childress M, Valladares O, Dragomir I, et al. HAMR: high-throughput annotation of modified ribonucleotides. Rna-a Publication of the Rna Society. 2013;19(12):1684-92.
-
(2013)
Rna-a Publication of the Rna Society
, vol.19
, Issue.12
, pp. 1684-1692
-
-
Ryvkin, P.1
Leung, Y.Y.2
Silverman, I.M.3
Childress, M.4
Valladares, O.5
Dragomir, I.6
-
23
-
-
0037407933
-
Identification of the yeast gene encoding the tRNA m1G methyltransferase responsible for modification at position 9
-
Jackman JE, Montange RK, Malik HS, Phizicky EM. Identification of the yeast gene encoding the tRNA m1G methyltransferase responsible for modification at position 9. RNA. 2003;9(5):574-85.
-
(2003)
RNA
, vol.9
, Issue.5
, pp. 574-585
-
-
Jackman, J.E.1
Montange, R.K.2
Malik, H.S.3
Phizicky, E.M.4
-
24
-
-
84883140214
-
Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
-
Alazami AM, Hijazi H, Al-Dosari MS, Shaheen R, Hashem A, Aldahmesh MA, et al. Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus. J Med Genet. 2013;50(7):425-30.
-
(2013)
J Med Genet
, vol.50
, Issue.7
, pp. 425-430
-
-
Alazami, A.M.1
Hijazi, H.2
Al-Dosari, M.S.3
Shaheen, R.4
Hashem, A.5
Aldahmesh, M.A.6
-
25
-
-
84860741715
-
Mutations in NSUN2 cause autosomal-recessive intellectual disability
-
Abbasi-Moheb L, Mertel S, Gonsior M, Nouri-Vahid L, Kahrizi K, Cirak S, et al. Mutations in NSUN2 cause autosomal-recessive intellectual disability. Am J Hum Genet. 2012;90(5):847-55.
-
(2012)
Am J Hum Genet
, vol.90
, Issue.5
, pp. 847-855
-
-
Abbasi-Moheb, L.1
Mertel, S.2
Gonsior, M.3
Nouri-Vahid, L.4
Kahrizi, K.5
Cirak, S.6
-
26
-
-
80053906761
-
Deep sequencing reveals 50 novel genes for recessive cognitive disorders
-
Najmabadi H, Hu H, Garshasbi M, Zemojtel T, Abedini SS, Chen W, et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011;478(7367):57-63.
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 57-63
-
-
Najmabadi, H.1
Hu, H.2
Garshasbi, M.3
Zemojtel, T.4
Abedini, S.S.5
Chen, W.6
-
27
-
-
33646552414
-
The RNA methyltransferase Misu (NSun2) mediates Myc-induced proliferation and is upregulated in tumors
-
Frye M, Watt FM. The RNA methyltransferase Misu (NSun2) mediates Myc-induced proliferation and is upregulated in tumors. Curr Biol. 2006;16(10):971-81.
-
(2006)
Curr Biol
, vol.16
, Issue.10
, pp. 971-981
-
-
Frye, M.1
Watt, F.M.2
-
28
-
-
77951811915
-
Distinct high resolution genome profiles of early onset and late onset colorectal cancer integrated with gene expression data identify candidate susceptibility loci
-
Berg M, Agesen TH, Thiis-Evensen E, Merok MA, Teixeira MR, Vatn MH, et al. Distinct high resolution genome profiles of early onset and late onset colorectal cancer integrated with gene expression data identify candidate susceptibility loci. Mol Cancer. 2010;9:100.
-
(2010)
Mol Cancer
, vol.9
, pp. 100
-
-
Berg, M.1
Agesen, T.H.2
Thiis-Evensen, E.3
Merok, M.A.4
Teixeira, M.R.5
Vatn, M.H.6
-
29
-
-
78650892625
-
Mammostrat as a tool to stratify breast cancer patients at risk of recurrence during endocrine therapy
-
Bartlett JM, Thomas J, Ross DT, Seitz RS, Ring BZ, Beck RA, et al. Mammostrat as a tool to stratify breast cancer patients at risk of recurrence during endocrine therapy. Breast Cancer Res. 2010;12(4):R47.
-
(2010)
Breast Cancer Res
, vol.12
, Issue.4
, pp. R47
-
-
Bartlett, J.M.1
Thomas, J.2
Ross, D.T.3
Seitz, R.S.4
Ring, B.Z.5
Beck, R.A.6
-
30
-
-
80052375980
-
Deficit of tRNA(Lys) modification by Cdkal1 causes the development of type 2 diabetes in mice
-
Wei FY, Suzuki T, Watanabe S, Kimura S, Kaitsuka T, Fujimura A, et al. Deficit of tRNA(Lys) modification by Cdkal1 causes the development of type 2 diabetes in mice. J Clin Invest. 2011;121(9):3598-608.
-
(2011)
J Clin Invest
, vol.121
, Issue.9
, pp. 3598-3608
-
-
Wei, F.Y.1
Suzuki, T.2
Watanabe, S.3
Kimura, S.4
Kaitsuka, T.5
Fujimura, A.6
-
31
-
-
41149178492
-
Polymorphisms in the TCF7L2, CDKAL1 and SLC30A8 genes are associated with impaired proinsulin conversion
-
Kirchhoff K, Machicao F, Haupt A, Schafer SA, Tschritter O, Staiger H, et al. Polymorphisms in the TCF7L2, CDKAL1 and SLC30A8 genes are associated with impaired proinsulin conversion. Diabetologia. 2008;51(4):597-601.
-
(2008)
Diabetologia
, vol.51
, Issue.4
, pp. 597-601
-
-
Kirchhoff, K.1
Machicao, F.2
Haupt, A.3
Schafer, S.A.4
Tschritter, O.5
Staiger, H.6
-
32
-
-
40949087723
-
Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population
-
Omori S, Tanaka Y, Takahashi A, Hirose H, Kashiwagi A, Kaku K, et al. Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 with susceptibility to type 2 diabetes in a Japanese population. Diabetes. 2008;57(3):791-5.
-
(2008)
Diabetes
, vol.57
, Issue.3
, pp. 791-795
-
-
Omori, S.1
Tanaka, Y.2
Takahashi, A.3
Hirose, H.4
Kashiwagi, A.5
Kaku, K.6
-
33
-
-
0034635519
-
Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu) (UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
-
Yasukawa T, Suzuki T, Ueda T, Ohta S, Watanabe K. Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu) (UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. J Biol Chem. 2000;275(6):4251-7.
-
(2000)
J Biol Chem
, vol.275
, Issue.6
, pp. 4251-4257
-
-
Yasukawa, T.1
Suzuki, T.2
Ueda, T.3
Ohta, S.4
Watanabe, K.5
-
34
-
-
21144455795
-
Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases
-
Yasukawa T, Kirino Y, Ishii N, Holt IJ, Jacobs HT, Makifuchi T, et al. Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases. FEBS Lett. 2005;579(13):2948-52.
-
(2005)
FEBS Lett
, vol.579
, Issue.13
, pp. 2948-2952
-
-
Yasukawa, T.1
Kirino, Y.2
Ishii, N.3
Holt, I.J.4
Jacobs, H.T.5
Makifuchi, T.6
-
35
-
-
18844430007
-
Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease
-
Kirino Y, Goto Y, Campos Y, Arenas J, Suzuki T. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease. Proc Natl Acad Sci U S A. 2005;102(20):7127-32.
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, Issue.20
, pp. 7127-7132
-
-
Kirino, Y.1
Goto, Y.2
Campos, Y.3
Arenas, J.4
Suzuki, T.5
-
36
-
-
0842285640
-
Ineffective hematopoiesis linked with a mitochondrial tRNA mutation (G3242A) in a patient with myelodysplastic syndrome
-
Gattermann N, Wulfert M, Junge B, Germing U, Haas R, Hofhaus G. Ineffective hematopoiesis linked with a mitochondrial tRNA mutation (G3242A) in a patient with myelodysplastic syndrome. Blood. 2004;103(4):1499-502.
-
(2004)
Blood
, vol.103
, Issue.4
, pp. 1499-1502
-
-
Gattermann, N.1
Wulfert, M.2
Junge, B.3
Germing, U.4
Haas, R.5
Hofhaus, G.6
-
37
-
-
84885010257
-
Methylation of promoters of microRNAs and their host genes in myelodysplastic syndromes
-
Erdogan B, Bosompem A, Peng D, Han L, Smith E, Kennedy ME, et al. Methylation of promoters of microRNAs and their host genes in myelodysplastic syndromes. Leukemia & lymphoma. 2013;54:2720-7.
-
(2013)
Leukemia & lymphoma
, vol.54
, pp. 2720-2727
-
-
Erdogan, B.1
Bosompem, A.2
Peng, D.3
Han, L.4
Smith, E.5
Kennedy, M.E.6
-
38
-
-
80051475292
-
Diagnostic microRNAs in myelodysplastic syndrome
-
Erdogan B, Facey C, Qualtieri J, Tedesco J, Rinker E, Isett RB, et al. Diagnostic microRNAs in myelodysplastic syndrome. Exp Hematol. 2011;39(9):915-26:e912.
-
(2011)
Exp Hematol
, vol.39
, Issue.9
, pp. 915-926
-
-
Erdogan, B.1
Facey, C.2
Qualtieri, J.3
Tedesco, J.4
Rinker, E.5
Isett, R.B.6
-
39
-
-
79959851207
-
Incidence of the myelodysplastic syndromes using a novel claims-based algorithm: high number of uncaptured cases by cancer registries
-
Cogle CR, Craig BM, Rollison DE, List AF. Incidence of the myelodysplastic syndromes using a novel claims-based algorithm: high number of uncaptured cases by cancer registries. Blood. 2011;117(26):7121-5.
-
(2011)
Blood
, vol.117
, Issue.26
, pp. 7121-7125
-
-
Cogle, C.R.1
Craig, B.M.2
Rollison, D.E.3
List, A.F.4
-
40
-
-
38349088899
-
Identification of RPS14 as a 5q- syndrome gene by RNA interference screen
-
Ebert BL, Pretz J, Bosco J, Chang CY, Tamayo P, Galili N, et al. Identification of RPS14 as a 5q- syndrome gene by RNA interference screen. Nature. 2008;451(7176):335-9.
-
(2008)
Nature
, vol.451
, Issue.7176
, pp. 335-339
-
-
Ebert, B.L.1
Pretz, J.2
Bosco, J.3
Chang, C.Y.4
Tamayo, P.5
Galili, N.6
-
41
-
-
73849121794
-
Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype
-
Starczynowski DT, Kuchenbauer F, Argiropoulos B, Sung S, Morin R, Muranyi A, et al. Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype. Nat Med. 2010;16(1):49-58.
-
(2010)
Nat Med
, vol.16
, Issue.1
, pp. 49-58
-
-
Starczynowski, D.T.1
Kuchenbauer, F.2
Argiropoulos, B.3
Sung, S.4
Morin, R.5
Muranyi, A.6
-
42
-
-
79951813573
-
Distinctive microRNA expression profiles in CD34+ bone marrow cells from patients with myelodysplastic syndrome
-
Dostalova Merkerova M, Krejcik Z, Votavova H, Belickova M, Vasikova A, Cermak J. Distinctive microRNA expression profiles in CD34+ bone marrow cells from patients with myelodysplastic syndrome. Eur J Hum Genet. 2011;19(3):313-9.
-
(2011)
Eur J Hum Genet
, vol.19
, Issue.3
, pp. 313-319
-
-
Dostalova Merkerova, M.1
Krejcik, Z.2
Votavova, H.3
Belickova, M.4
Vasikova, A.5
Cermak, J.6
-
43
-
-
77955274827
-
Aberrant microRNA expression pattern in myelodysplastic bone marrow cells
-
Hussein K, Theophile K, Busche G, Schlegelberger B, Gohring G, Kreipe H, et al. Aberrant microRNA expression pattern in myelodysplastic bone marrow cells. Leuk Res. 2010;34(9):1169-74.
-
(2010)
Leuk Res
, vol.34
, Issue.9
, pp. 1169-1174
-
-
Hussein, K.1
Theophile, K.2
Busche, G.3
Schlegelberger, B.4
Gohring, G.5
Kreipe, H.6
-
44
-
-
71049175699
-
Hematopoiesis-related microRNA expression in myelodysplastic syndromes
-
Pons A, Nomdedeu B, Navarro A, Gaya A, Gel B, Diaz T, et al. Hematopoiesis-related microRNA expression in myelodysplastic syndromes. Leuk Lymphoma. 2009;50:1854-9.
-
(2009)
Leuk Lymphoma
, vol.50
, pp. 1854-1859
-
-
Pons, A.1
Nomdedeu, B.2
Navarro, A.3
Gaya, A.4
Gel, B.5
Diaz, T.6
-
45
-
-
79952587193
-
Identification of a risk dependent microRNA expression signature in myelodysplastic syndromes
-
Sokol L, Caceres G, Volinia S, Alder H, Nuovo GJ, Liu CG, et al. Identification of a risk dependent microRNA expression signature in myelodysplastic syndromes. Br J Haematol. 2011;153(1):24-32.
-
(2011)
Br J Haematol
, vol.153
, Issue.1
, pp. 24-32
-
-
Sokol, L.1
Caceres, G.2
Volinia, S.3
Alder, H.4
Nuovo, G.J.5
Liu, C.G.6
-
46
-
-
34247172535
-
Myelodysplastic syndromes: incidence and survival in the United States
-
Ma X, Does M, Raza A, Mayne ST. Myelodysplastic syndromes: incidence and survival in the United States. Cancer. 2007;109(8):1536-42.
-
(2007)
Cancer
, vol.109
, Issue.8
, pp. 1536-1542
-
-
Ma, X.1
Does, M.2
Raza, A.3
Mayne, S.T.4
-
47
-
-
67649477391
-
World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues
-
4th ed. Lyon, France: IARC Press
-
Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. World Health Organization Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th ed. Lyon, France: IARC Press; 2008.
-
(2008)
-
-
Swerdlow, S.H.1
Campo, E.2
Harris, N.L.3
Jaffe, E.S.4
Pileri, S.A.5
Stein, H.6
-
48
-
-
33748474416
-
Further analysis of trials with azacitidine in patients with myelodysplastic syndrome: studies 8421, 8921, and 9221 by the Cancer and Leukemia Group B
-
Silverman LR, McKenzie DR, Peterson BL, Holland JF, Backstrom JT, Beach CL, et al. Further analysis of trials with azacitidine in patients with myelodysplastic syndrome: studies 8421, 8921, and 9221 by the Cancer and Leukemia Group B. J Clin Oncol. 2006;24(24):3895-903.
-
(2006)
J Clin Oncol
, vol.24
, Issue.24
, pp. 3895-3903
-
-
Silverman, L.R.1
McKenzie, D.R.2
Peterson, B.L.3
Holland, J.F.4
Backstrom, J.T.5
Beach, C.L.6
-
49
-
-
84908247072
-
TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients
-
Bejar R, Lord A, Stevenson K, Bar-Natan M, Perez-Ladaga A, Zaneveld J, et al. TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients. Blood. 2014;124(17):2705-12.
-
(2014)
Blood
, vol.124
, Issue.17
, pp. 2705-2712
-
-
Bejar, R.1
Lord, A.2
Stevenson, K.3
Bar-Natan, M.4
Perez-Ladaga, A.5
Zaneveld, J.6
-
50
-
-
84885571972
-
Prognostic impact of the number of methylated genes in myelodysplastic syndromes and acute myeloid leukemias treated with azacytidine
-
Abaigar M, Ramos F, Benito R, Diez-Campelo M, Sanchez-del-Real J, Hermosin L, et al. Prognostic impact of the number of methylated genes in myelodysplastic syndromes and acute myeloid leukemias treated with azacytidine. Ann Hematol. 2013;92(11):1543-52.
-
(2013)
Ann Hematol
, vol.92
, Issue.11
, pp. 1543-1552
-
-
Abaigar, M.1
Ramos, F.2
Benito, R.3
Diez-Campelo, M.4
Sanchez-del-Real, J.5
Hermosin, L.6
-
51
-
-
84895785721
-
Expression of nucleoside-metabolizing enzymes in myelodysplastic syndromes and modulation of response to azacitidine
-
Valencia A, Masala E, Rossi A, Martino A, Sanna A, Buchi F, et al. Expression of nucleoside-metabolizing enzymes in myelodysplastic syndromes and modulation of response to azacitidine. Leukemia. 2014;28(3):621-8.
-
(2014)
Leukemia
, vol.28
, Issue.3
, pp. 621-628
-
-
Valencia, A.1
Masala, E.2
Rossi, A.3
Martino, A.4
Sanna, A.5
Buchi, F.6
-
52
-
-
70350720044
-
MDS and secondary AML display unique patterns and abundance of aberrant DNA methylation
-
Figueroa ME, Skrabanek L, Li Y, Jiemjit A, Fandy TE, Paietta E, et al. MDS and secondary AML display unique patterns and abundance of aberrant DNA methylation. Blood. 2009;114(16):3448-58.
-
(2009)
Blood
, vol.114
, Issue.16
, pp. 3448-3458
-
-
Figueroa, M.E.1
Skrabanek, L.2
Li, Y.3
Jiemjit, A.4
Fandy, T.E.5
Paietta, E.6
-
53
-
-
67349200930
-
The DNA methyltransferase inhibitors azacitidine, decitabine and zebularine exert differential effects on cancer gene expression in acute myeloid leukemia cells
-
Flotho C, Claus R, Batz C, Schneider M, Sandrock I, Ihde S, et al. The DNA methyltransferase inhibitors azacitidine, decitabine and zebularine exert differential effects on cancer gene expression in acute myeloid leukemia cells. Leukemia. 2009;23(6):1019-28.
-
(2009)
Leukemia
, vol.23
, Issue.6
, pp. 1019-1028
-
-
Flotho, C.1
Claus, R.2
Batz, C.3
Schneider, M.4
Sandrock, I.5
Ihde, S.6
-
54
-
-
23844557794
-
Characterization of DNA demethylation effects induced by 5-Aza-2'-deoxycytidine in patients with myelodysplastic syndrome
-
Mund C, Hackanson B, Stresemann C, Lubbert M, Lyko F. Characterization of DNA demethylation effects induced by 5-Aza-2'-deoxycytidine in patients with myelodysplastic syndrome. Cancer Res. 2005;65(16):7086-90.
-
(2005)
Cancer Res
, vol.65
, Issue.16
, pp. 7086-7090
-
-
Mund, C.1
Hackanson, B.2
Stresemann, C.3
Lubbert, M.4
Lyko, F.5
-
55
-
-
84928982643
-
Specific molecular signatures predict decitabine response in chronic myelomonocytic leukemia
-
Meldi K, Qin T, Buchi F, Droin N, Sotzen J, Micol JB, et al. Specific molecular signatures predict decitabine response in chronic myelomonocytic leukemia. J Clin Invest. 2015;125(5):1857-72.
-
(2015)
J Clin Invest
, vol.125
, Issue.5
, pp. 1857-1872
-
-
Meldi, K.1
Qin, T.2
Buchi, F.3
Droin, N.4
Sotzen, J.5
Micol, J.B.6
-
56
-
-
33745968917
-
Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia
-
Cheson BD, Greenberg PL, Bennett JM, Lowenberg B, Wijermans PW, Nimer SD, et al. Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia. Blood. 2006;108(2):419-25.
-
(2006)
Blood
, vol.108
, Issue.2
, pp. 419-425
-
-
Cheson, B.D.1
Greenberg, P.L.2
Bennett, J.M.3
Lowenberg, B.4
Wijermans, P.W.5
Nimer, S.D.6
-
57
-
-
80255127234
-
Cutadapt removes adapter sequences from high-throughput sequencing reads
-
Martin M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnetjournal. 2011;17:10-2.
-
(2011)
EMBnetjournal
, vol.17
, pp. 10-12
-
-
Martin, M.1
-
58
-
-
84902189696
-
Multi-perspective quality control of Illumina exome sequencing data using QC3
-
Guo Y, Zhao S, Sheng Q, Ye F, Li J, Lehmann B, et al. Multi-perspective quality control of Illumina exome sequencing data using QC3. Genomics. 2014;103:323-8.
-
(2014)
Genomics
, vol.103
, pp. 323-328
-
-
Guo, Y.1
Zhao, S.2
Sheng, Q.3
Ye, F.4
Li, J.5
Lehmann, B.6
-
59
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10(3):R25.
-
(2009)
Genome Biol
, vol.10
, Issue.3
, pp. R25
-
-
Langmead, B.1
Trapnell, C.2
Pop, M.3
Salzberg, S.L.4
-
60
-
-
84891818318
-
miRBase: annotating high confidence microRNAs using deep sequencing data
-
Kozomara A, Griffiths-Jones S. miRBase: annotating high confidence microRNAs using deep sequencing data. Nucleic Acids Res. 2014;42(Database issue):D68-73.
-
(2014)
Nucleic Acids Res
, vol.42
, Issue.DATABASE ISSUE
, pp. D68-73
-
-
Kozomara, A.1
Griffiths-Jones, S.2
-
61
-
-
84891768365
-
Ensembl 2014
-
Flicek P, Amode MR, Barrell D, Beal K, Billis K, Brent S, et al. Ensembl 2014. Nucleic Acids Res. 2014;42(Database issue):D749-55.
-
(2014)
Nucleic Acids Res
, vol.42
, Issue.DATABASE ISSUE
, pp. D749-D755
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Billis, K.5
Brent, S.6
-
62
-
-
84875286904
-
RNA-seq-based mapping and candidate identification of mutations from forward genetic screens
-
Miller AC, Obholzer ND, Shah AN, Megason SG, Moens CB. RNA-seq-based mapping and candidate identification of mutations from forward genetic screens. Genome Res. 2013;23(4):679-86.
-
(2013)
Genome Res
, vol.23
, Issue.4
, pp. 679-686
-
-
Miller, A.C.1
Obholzer, N.D.2
Shah, A.N.3
Megason, S.G.4
Moens, C.B.5
-
63
-
-
84860505950
-
Towards accurate detection and genotyping of expressed variants from whole transcriptome sequencing data
-
Duitama J, Srivastava P, Mandoiu I. Towards accurate detection and genotyping of expressed variants from whole transcriptome sequencing data. BMC Genomics. 2012;13 Suppl 2:S6.
-
(2012)
BMC Genomics
, vol.13
, pp. S6
-
-
Duitama, J.1
Srivastava, P.2
Mandoiu, I.3
-
64
-
-
84885300845
-
Reliable Identification of Genomic Variants from RNA-Seq Data
-
Piskol R, Ramaswami G, Li JB. Reliable Identification of Genomic Variants from RNA-Seq Data. Am J Hum Genet. 2013;93(4):641-51.
-
(2013)
Am J Hum Genet
, vol.93
, Issue.4
, pp. 641-651
-
-
Piskol, R.1
Ramaswami, G.2
Li, J.B.3
-
65
-
-
84863229597
-
VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt DC, Zhang Q, Larson DE, Shen D, McLellan MD, Lin L, et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res. 2012;22(3):568-76.
-
(2012)
Genome Res
, vol.22
, Issue.3
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
Lin, L.6
-
66
-
-
84902203573
-
MultiRankSeq: Multiperspective Approach for RNAseq Differential Expression Analysis and Quality Control
-
Guo Y, Zhao S, Ye F, Sheng Q, Shyr Y. MultiRankSeq: Multiperspective Approach for RNAseq Differential Expression Analysis and Quality Control. BioMed Res International. 2014;2014:8.
-
(2014)
BioMed Res International
, vol.2014
, pp. 8
-
-
Guo, Y.1
Zhao, S.2
Ye, F.3
Sheng, Q.4
Shyr, Y.5
-
67
-
-
77958471357
-
Differential expression analysis for sequence count data
-
Anders S, Huber W. Differential expression analysis for sequence count data. Genome Biol. 2010;11(10):R106.
-
(2010)
Genome Biol
, vol.11
, Issue.10
, pp. R106
-
-
Anders, S.1
Huber, W.2
-
68
-
-
75249087100
-
edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
-
Robinson MD, McCarthy DJ, Smyth GK. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics. 2010;26(1):139-40.
-
(2010)
Bioinformatics
, vol.26
, Issue.1
, pp. 139-140
-
-
Robinson, M.D.1
McCarthy, D.J.2
Smyth, G.K.3
-
69
-
-
77955298482
-
baySeq: empirical Bayesian methods for identifying differential expression in sequence count data
-
Hardcastle TJ, Kelly KA. baySeq: empirical Bayesian methods for identifying differential expression in sequence count data. BMC Bioinformatics. 2010;11:422.
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 422
-
-
Hardcastle, T.J.1
Kelly, K.A.2
-
70
-
-
28044450144
-
Regularization and variable selection via the elastic net (vol B 67, pg 301, 2005)
-
Zou H, Hastie T. Regularization and variable selection via the elastic net (vol B 67, pg 301, 2005). J Royal Stat Soc Series B-Stat Method. 2005;67:768.
-
(2005)
J Royal Stat Soc Series B-Stat Method
, vol.67
, pp. 768
-
-
Zou, H.1
Hastie, T.2
-
71
-
-
85194972808
-
Regression shrinkage and selection via the Lasso
-
Tibshirani R. Regression shrinkage and selection via the Lasso. J Royal Stat Soc Series B-Stat Method. 1996;58(1):267-88.
-
(1996)
J Royal Stat Soc Series B-Stat Method
, vol.58
, Issue.1
, pp. 267-288
-
-
Tibshirani, R.1
-
73
-
-
77950236668
-
Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction
-
Chen ML, Logan TD, Hochberg ML, Shelat SG, Yu X, Wilding GE, et al. Erythroid dysplasia, megaloblastic anemia, and impaired lymphopoiesis arising from mitochondrial dysfunction. Blood. 2009;114(19):4045-53.
-
(2009)
Blood
, vol.114
, Issue.19
, pp. 4045-4053
-
-
Chen, M.L.1
Logan, T.D.2
Hochberg, M.L.3
Shelat, S.G.4
Yu, X.5
Wilding, G.E.6
-
74
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch JS, Ley TJ, Link DC, Miller CA, Larson DE, Koboldt DC, et al. The origin and evolution of mutations in acute myeloid leukemia. Cell. 2012;150(2):264-78.
-
(2012)
Cell
, vol.150
, Issue.2
, pp. 264-278
-
-
Welch, J.S.1
Ley, T.J.2
Link, D.C.3
Miller, C.A.4
Larson, D.E.5
Koboldt, D.C.6
-
75
-
-
84920024296
-
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence
-
Genovese G, Kahler AK, Handsaker RE, Lindberg J, Rose SA, Bakhoum SF, et al. Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. N Engl J Med. 2014;371(26):2477-87.
-
(2014)
N Engl J Med
, vol.371
, Issue.26
, pp. 2477-2487
-
-
Genovese, G.1
Kahler, A.K.2
Handsaker, R.E.3
Lindberg, J.4
Rose, S.A.5
Bakhoum, S.F.6
-
76
-
-
84920053873
-
Age-related clonal hematopoiesis associated with adverse outcomes
-
Jaiswal S, Fontanillas P, Flannick J, Manning A, Grauman PV, Mar BG, et al. Age-related clonal hematopoiesis associated with adverse outcomes. N Engl J Med. 2014;371(26):2488-98.
-
(2014)
N Engl J Med
, vol.371
, Issue.26
, pp. 2488-2498
-
-
Jaiswal, S.1
Fontanillas, P.2
Flannick, J.3
Manning, A.4
Grauman, P.V.5
Mar, B.G.6
-
77
-
-
84930003179
-
Age-related mutations associated with clonal hematopoietic expansion and malignancies
-
Xie M, Lu C, Wang J, McLellan MD, Johnson KJ, Wendl MC, et al. Age-related mutations associated with clonal hematopoietic expansion and malignancies. Nat Med. 2014;20(12):1472-8.
-
(2014)
Nat Med
, vol.20
, Issue.12
, pp. 1472-1478
-
-
Xie, M.1
Lu, C.2
Wang, J.3
McLellan, M.D.4
Johnson, K.J.5
Wendl, M.C.6
-
78
-
-
0024273119
-
The accuracy of reverse transcriptase from HIV-1
-
Roberts JD, Bebenek K, Kunkel TA. The accuracy of reverse transcriptase from HIV-1. Science. 1988;242(4882):1171-3.
-
(1988)
Science
, vol.242
, Issue.4882
, pp. 1171-1173
-
-
Roberts, J.D.1
Bebenek, K.2
Kunkel, T.A.3
-
79
-
-
84938415138
-
Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer
-
O'Brien TD, Jia P, Xia J, Saxena U, Jin H, Vuong H, et al. Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer. Methods. 2015;83:118-27.
-
(2015)
Methods
, vol.83
, pp. 118-127
-
-
O'Brien, T.D.1
Jia, P.2
Xia, J.3
Saxena, U.4
Jin, H.5
Vuong, H.6
-
80
-
-
84879286291
-
Thermostable group II intron reverse transcriptase fusion proteins and their use in cDNA synthesis and next-generation RNA sequencing
-
Mohr S, Ghanem E, Smith W, Sheeter D, Qin Y, King O, et al. Thermostable group II intron reverse transcriptase fusion proteins and their use in cDNA synthesis and next-generation RNA sequencing. RNA. 2013;19(7):958-70.
-
(2013)
RNA
, vol.19
, Issue.7
, pp. 958-970
-
-
Mohr, S.1
Ghanem, E.2
Smith, W.3
Sheeter, D.4
Qin, Y.5
King, O.6
-
81
-
-
84892424438
-
Biotechnological applications of mobile group II introns and their reverse transcriptases: gene targeting, RNA-seq, and non-coding RNA analysis
-
Enyeart PJ, Mohr G, Ellington AD, Lambowitz AM. Biotechnological applications of mobile group II introns and their reverse transcriptases: gene targeting, RNA-seq, and non-coding RNA analysis. Mob DNA. 2014;5:2.
-
(2014)
Mob DNA
, vol.5
, pp. 2
-
-
Enyeart, P.J.1
Mohr, G.2
Ellington, A.D.3
Lambowitz, A.M.4
-
82
-
-
84922479672
-
Rqc2p and 60S ribosomal subunits mediate mRNA-independent elongation of nascent chains
-
Shen PS, Park J, Qin YD, Li XM, Parsawar K, Larson MH, et al. Rqc2p and 60S ribosomal subunits mediate mRNA-independent elongation of nascent chains. Science. 2015;347(6217):75-8.
-
(2015)
Science
, vol.347
, Issue.6217
, pp. 75-78
-
-
Shen, P.S.1
Park, J.2
Qin, Y.D.3
Li, X.M.4
Parsawar, K.5
Larson, M.H.6
-
83
-
-
84906308938
-
Broad and adaptable RNA structure recognition by the human interferon-induced tetratricopeptide repeat protein IFIT5
-
Katibah GE, Qin YD, Sidote DJ, Yao J, Lambowitz AM, Collins K. Broad and adaptable RNA structure recognition by the human interferon-induced tetratricopeptide repeat protein IFIT5. Proc Natl Acad Sci U S A. 2014;111(33):12025-30.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, Issue.33
, pp. 12025-12030
-
-
Katibah, G.E.1
Qin, Y.D.2
Sidote, D.J.3
Yao, J.4
Lambowitz, A.M.5
Collins, K.6
-
84
-
-
65249129859
-
Angiogenin cleaves tRNA and promotes stress-induced translational repression
-
Yamasaki S, Ivanov P, Hu GF, Anderson P. Angiogenin cleaves tRNA and promotes stress-induced translational repression. J Cell Biol. 2009;185(1):35-42.
-
(2009)
J Cell Biol
, vol.185
, Issue.1
, pp. 35-42
-
-
Yamasaki, S.1
Ivanov, P.2
Hu, G.F.3
Anderson, P.4
-
85
-
-
84904248961
-
Inactivation of p53 Is Insufficient to Allow B Cells and B-Cell Lymphomas to Survive Without Dicer
-
Adams CM, Eischen CM. Inactivation of p53 Is Insufficient to Allow B Cells and B-Cell Lymphomas to Survive Without Dicer. Cancer Res. 2014;74(14):3923-34.
-
(2014)
Cancer Res
, vol.74
, Issue.14
, pp. 3923-3934
-
-
Adams, C.M.1
Eischen, C.M.2
-
86
-
-
84872958116
-
Cancer-associated somatic DICER1 hotspot mutations cause defective miRNA processing and reverse-strand expression bias to predominantly mature 3p strands through loss of 5p strand cleavage
-
Anglesio MS, Wang Y, Yang W, Senz J, Wan A, Heravi-Moussavi A, et al. Cancer-associated somatic DICER1 hotspot mutations cause defective miRNA processing and reverse-strand expression bias to predominantly mature 3p strands through loss of 5p strand cleavage. J Pathol. 2013;229(3):400-9.
-
(2013)
J Pathol
, vol.229
, Issue.3
, pp. 400-409
-
-
Anglesio, M.S.1
Wang, Y.2
Yang, W.3
Senz, J.4
Wan, A.5
Heravi-Moussavi, A.6
-
87
-
-
84862908497
-
Recurrent somatic DICER1 mutations in nonepithelial ovarian cancers
-
Heravi-Moussavi A, Anglesio MS, Cheng SW, Senz J, Yang W, Prentice L, et al. Recurrent somatic DICER1 mutations in nonepithelial ovarian cancers. N Engl J Med. 2012;366(3):234-42.
-
(2012)
N Engl J Med
, vol.366
, Issue.3
, pp. 234-242
-
-
Heravi-Moussavi, A.1
Anglesio, M.S.2
Cheng, S.W.3
Senz, J.4
Yang, W.5
Prentice, L.6
-
88
-
-
0027865639
-
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene
-
Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, et al. A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene. Eur J Hum Genet. 1993;1(1):80-7.
-
(1993)
Eur J Hum Genet
, vol.1
, Issue.1
, pp. 80-87
-
-
Zeviani, M.1
Muntoni, F.2
Savarese, N.3
Serra, G.4
Tiranti, V.5
Carrara, F.6
-
89
-
-
84862180122
-
Mitochondrial DNA-Associated Leigh Syndrome and NARP
-
Seattle: University of Washington
-
Thorburn DR, Rahman S. Mitochondrial DNA-Associated Leigh Syndrome and NARP. Seattle: University of Washington; 1993.
-
(1993)
-
-
Thorburn, D.R.1
Rahman, S.2
-
90
-
-
36649033365
-
A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy
-
Mahjoub S, Sternberg D, Boussaada R, Filaut S, Gmira F, Mechmech R, et al. A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy. Diagn Mol Pathol. 2007;16(4):238-42.
-
(2007)
Diagn Mol Pathol
, vol.16
, Issue.4
, pp. 238-242
-
-
Mahjoub, S.1
Sternberg, D.2
Boussaada, R.3
Filaut, S.4
Gmira, F.5
Mechmech, R.6
-
91
-
-
0035852868
-
Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation
-
Bataillard M, Chatzoglou E, Rumbach L, Sternberg D, Tournade A, Laforet P, et al. Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation. Neurology. 2001;56(3):405-7.
-
(2001)
Neurology
, vol.56
, Issue.3
, pp. 405-407
-
-
Bataillard, M.1
Chatzoglou, E.2
Rumbach, L.3
Sternberg, D.4
Tournade, A.5
Laforet, P.6
-
92
-
-
0031801084
-
A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance
-
Vissing J, Salamon MB, Arlien-Soborg P, Norby S, Manta P, DiMauro S, et al. A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance. Neurology. 1998;50(6):1875-8.
-
(1998)
Neurology
, vol.50
, Issue.6
, pp. 1875-1878
-
-
Vissing, J.1
Salamon, M.B.2
Arlien-Soborg, P.3
Norby, S.4
Manta, P.5
DiMauro, S.6
-
93
-
-
84865003520
-
New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset
-
del Mar O'CM, Emperador S, Lopez-Gallardo E, Jou C, Bujan N, Montero R, et al. New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. Neurogenetics. 2012;13(3):245-50.
-
(2012)
Neurogenetics
, vol.13
, Issue.3
, pp. 245-250
-
-
Mar, O.C.M.1
Emperador, S.2
Lopez-Gallardo, E.3
Jou, C.4
Bujan, N.5
Montero, R.6
-
94
-
-
77950520149
-
Maternally inherited hearing loss is associated with the novel mitochondrial tRNA(Ser(UCN)) 7505 T > C mutation in a Han Chinese family
-
Tang XW, Li RH, Zheng J, Cai Q, Zhang T, Gong SS, et al. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA(Ser(UCN)) 7505 T > C mutation in a Han Chinese family. Mol Genet Metab. 2010;100(1):57-64.
-
(2010)
Mol Genet Metab
, vol.100
, Issue.1
, pp. 57-64
-
-
Tang, X.W.1
Li, R.H.2
Zheng, J.3
Cai, Q.4
Zhang, T.5
Gong, S.S.6
-
95
-
-
0027960070
-
Chronic Progressive External Ophthalmoplegia Is Associated with a Novel Mutation in the Mitochondrial Trna(Asn) Gene
-
Seibel P, Lauber J, Klopstock T, Marsac C, Kadenbach B, Reichmann H. Chronic Progressive External Ophthalmoplegia Is Associated with a Novel Mutation in the Mitochondrial Trna(Asn) Gene. Biochem Bioph Res Co. 1994;204(2):482-9.
-
(1994)
Biochem Bioph Res Co
, vol.204
, Issue.2
, pp. 482-489
-
-
Seibel, P.1
Lauber, J.2
Klopstock, T.3
Marsac, C.4
Kadenbach, B.5
Reichmann, H.6
-
96
-
-
0043066954
-
Increased variation in mtDNA in patients with familial sensorineural hearing impairment
-
Lehtonen MS, Moilanen JS, Majamaa K. Increased variation in mtDNA in patients with familial sensorineural hearing impairment. Hum Genet. 2003;113(3):220-7.
-
(2003)
Hum Genet
, vol.113
, Issue.3
, pp. 220-227
-
-
Lehtonen, M.S.1
Moilanen, J.S.2
Majamaa, K.3
-
97
-
-
0242594752
-
Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis
-
Scaglia F, Vogel H, Hawkins EP, Vladutiu GD, Liu LL, Wong LJ. Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis. Am J Med Genet A. 2003;123A(2):172-8.
-
(2003)
Am J Med Genet A
, vol.123A
, Issue.2
, pp. 172-178
-
-
Scaglia, F.1
Vogel, H.2
Hawkins, E.P.3
Vladutiu, G.D.4
Liu, L.L.5
Wong, L.J.6
-
98
-
-
0035497972
-
In vitro 3 '-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness
-
Levinger L, Jacobs O, James M. In vitro 3 '-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness. Nucleic Acids Res. 2001;29(21):4334-40.
-
(2001)
Nucleic Acids Res
, vol.29
, Issue.21
, pp. 4334-4340
-
-
Levinger, L.1
Jacobs, O.2
James, M.3
-
99
-
-
24344481620
-
A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy
-
Seneca S, Goemans N, Van Coster R, Givron P, Reybrouck T, Sciot R, et al. A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy. Am J Med Genet A. 2005;137(2):170-5.
-
(2005)
Am J Med Genet A
, vol.137
, Issue.2
, pp. 170-175
-
-
Seneca, S.1
Goemans, N.2
Coster, R.3
Givron, P.4
Reybrouck, T.5
Sciot, R.6
-
100
-
-
6044249065
-
Mitochondrial tRNA 3 ' end metabolism and human disease
-
Levinger L, Morl M, Florentz C. Mitochondrial tRNA 3 ' end metabolism and human disease. Nucleic Acids Res. 2004;32(18):5430-41.
-
(2004)
Nucleic Acids Res
, vol.32
, Issue.18
, pp. 5430-5441
-
-
Levinger, L.1
Morl, M.2
Florentz, C.3
-
101
-
-
0028070162
-
Maternally Inherited Hypertrophic Cardiomyopathy Due to a Novel T-to-C Transition at Nucleotide-9997 in the Mitochondrial Trna(Glycine) Gene
-
Merante F, Tein I, Benson L, Robinson BH. Maternally Inherited Hypertrophic Cardiomyopathy Due to a Novel T-to-C Transition at Nucleotide-9997 in the Mitochondrial Trna(Glycine) Gene. Am J Hum Genet. 1994;55(3):437-46.
-
(1994)
Am J Hum Genet
, vol.55
, Issue.3
, pp. 437-446
-
-
Merante, F.1
Tein, I.2
Benson, L.3
Robinson, B.H.4
-
102
-
-
34447104140
-
Mitochondrial myopathy associated with a novel mutation in mtDNA
-
Pancrudo J, Shanske S, Coku J, Lu J, Mardach R, Akman O, et al. Mitochondrial myopathy associated with a novel mutation in mtDNA. Neuromuscul Disord. 2007;17(8):651-4.
-
(2007)
Neuromuscul Disord
, vol.17
, Issue.8
, pp. 651-654
-
-
Pancrudo, J.1
Shanske, S.2
Coku, J.3
Lu, J.4
Mardach, R.5
Akman, O.6
-
103
-
-
70350707763
-
Pathogenic Mitochondrial tRNA Mutations - Which Mutations Are Inherited and Why?
-
Elson JL, Swalwell H, Blakely EL, McFarland R, Taylor RW, Turnbull DM. Pathogenic Mitochondrial tRNA Mutations - Which Mutations Are Inherited and Why? Hum Mutat. 2009;30(11):E984-92.
-
(2009)
Hum Mutat
, vol.30
, Issue.11
, pp. E984-E992
-
-
Elson, J.L.1
Swalwell, H.2
Blakely, E.L.3
McFarland, R.4
Taylor, R.W.5
Turnbull, D.M.6
-
104
-
-
34548258173
-
A novel mutation in the mitochondrial tRNA (Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency
-
Wong LJC, Yim D, Bai RK, Kwon H, Vacek MM, Zane J, et al. A novel mutation in the mitochondrial tRNA (Ser(AGY)) gene associated with mitochondrial myopathy, encephalopathy, and complex I deficiency. J Med Genet. 2006;43(9):e46.
-
(2006)
J Med Genet
, vol.43
, Issue.9
, pp. e46
-
-
Wong, L.J.C.1
Yim, D.2
Bai, R.K.3
Kwon, H.4
Vacek, M.M.5
Zane, J.6
-
105
-
-
23044441831
-
Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism
-
Zsurka G, Schroder R, Kornblum C, Rudolph J, Wiesner RJ, Elger CE, et al. Tissue dependent co-segregation of the novel pathogenic G12276A mitochondrial tRNALeu(CUN) mutation with the A185G D-loop polymorphism. J Med Genet. 2004;41(12):e124.
-
(2004)
J Med Genet
, vol.41
, Issue.12
, pp. e124
-
-
Zsurka, G.1
Schroder, R.2
Kornblum, C.3
Rudolph, J.4
Wiesner, R.J.5
Elger, C.E.6
-
106
-
-
78650865715
-
Reversible infantile respiratory chain deficiency: a clinical and molecular study
-
Mimaki M, Hatakeyama H, Komaki H, Yokoyama M, Arai H, Kirino Y, et al. Reversible infantile respiratory chain deficiency: a clinical and molecular study. Ann Neurol. 2010;68(6):845-54.
-
(2010)
Ann Neurol
, vol.68
, Issue.6
, pp. 845-854
-
-
Mimaki, M.1
Hatakeyama, H.2
Komaki, H.3
Yokoyama, M.4
Arai, H.5
Kirino, Y.6
-
107
-
-
0029759665
-
Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement
-
Mayr-Wohlfart U, Paulus C, Henneberg A, Rodel G. Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement. Acta Neurol Scand. 1996;94(3):167-71.
-
(1996)
Acta Neurol Scand
, vol.94
, Issue.3
, pp. 167-171
-
-
Mayr-Wohlfart, U.1
Paulus, C.2
Henneberg, A.3
Rodel, G.4
-
108
-
-
0037110990
-
A cystic fibrosis patient with two novel mutations in mitochondrial DNA: Mild disease led to delayed diagnosis of both disorders
-
Wong LJC, Liang MH, Kwon H, Bai RK, Alper O, Gropman A. A cystic fibrosis patient with two novel mutations in mitochondrial DNA: Mild disease led to delayed diagnosis of both disorders. Am J Med Genet. 2002;113(1):59-64.
-
(2002)
Am J Med Genet
, vol.113
, Issue.1
, pp. 59-64
-
-
Wong, L.J.C.1
Liang, M.H.2
Kwon, H.3
Bai, R.K.4
Alper, O.5
Gropman, A.6
|