-
1
-
-
33846928760
-
Mitochondrial DNA sequence variants in epithelial ovarian tumor subtypes and stages
-
Aikhionbare F.O., Mehrabi S., Kumaresan K., Zavareh M., Olatinwo M., Odunsi K., Partridge E. Mitochondrial DNA sequence variants in epithelial ovarian tumor subtypes and stages. J. Carcinog. 2007, 6:1.
-
(2007)
J. Carcinog.
, vol.6
, pp. 1
-
-
Aikhionbare, F.O.1
Mehrabi, S.2
Kumaresan, K.3
Zavareh, M.4
Olatinwo, M.5
Odunsi, K.6
Partridge, E.7
-
2
-
-
40949085739
-
Mutations and polymorphisms in mitochondrial DNA in head and neck cancer cell lines
-
Allegra E., Garozzo A., Lombardo N., De Clemente M., Carey T.E. Mutations and polymorphisms in mitochondrial DNA in head and neck cancer cell lines. Acta Otorhinolaryngol. Ital. 2006, 26:185-190.
-
(2006)
Acta Otorhinolaryngol. Ital.
, vol.26
, pp. 185-190
-
-
Allegra, E.1
Garozzo, A.2
Lombardo, N.3
De Clemente, M.4
Carey, T.E.5
-
3
-
-
0025183708
-
Basic local alignment search tool
-
Altschul S.F., Gish W., Miller W., Myers E.W., Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 1990, 215:403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
4
-
-
0035358999
-
Mitochondrial pseudogenes: evolution's misplaced witnesses
-
Bensasson D., Zhang D., Hartl D.L., Hewitt G.M. Mitochondrial pseudogenes: evolution's misplaced witnesses. Trends Ecol. Evol. 2001, 16:314-321.
-
(2001)
Trends Ecol. Evol.
, vol.16
, pp. 314-321
-
-
Bensasson, D.1
Zhang, D.2
Hartl, D.L.3
Hewitt, G.M.4
-
5
-
-
0034237205
-
Organellar genes: why do they end up in the nucleus?
-
Blanchard J.L., Lynch M. Organellar genes: why do they end up in the nucleus?. Trends Genet. 2000, 16:315-320.
-
(2000)
Trends Genet.
, vol.16
, pp. 315-320
-
-
Blanchard, J.L.1
Lynch, M.2
-
6
-
-
77955418028
-
Mitochondrial DNA sequences are present inside nuclear DNA in rat tissues and increase with age
-
Caro P., Gomez J., Arduini A., Gonzalez-Sanchez M., Gonzalez-Garcia M., Borras C., Vina J., Puertas M.J., Sastre J., Barja G. Mitochondrial DNA sequences are present inside nuclear DNA in rat tissues and increase with age. Mitochondrion 2010, 10:479-486.
-
(2010)
Mitochondrion
, vol.10
, pp. 479-486
-
-
Caro, P.1
Gomez, J.2
Arduini, A.3
Gonzalez-Sanchez, M.4
Gonzalez-Garcia, M.5
Borras, C.6
Vina, J.7
Puertas, M.J.8
Sastre, J.9
Barja, G.10
-
7
-
-
0039250954
-
Facile detection of mitochondrial DNA mutations in tumors and bodily fluids
-
Fliss M.S., Usadel H., Caballero O.L., Wu L., Buta M.R., Eleff S.M., Jen J., Sidransky D. Facile detection of mitochondrial DNA mutations in tumors and bodily fluids. Science 2000, 287:2017-2019.
-
(2000)
Science
, vol.287
, pp. 2017-2019
-
-
Fliss, M.S.1
Usadel, H.2
Caballero, O.L.3
Wu, L.4
Buta, M.R.5
Eleff, S.M.6
Jen, J.7
Sidransky, D.8
-
8
-
-
34547480470
-
Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors
-
Gasparre G., Porcelli A.M., Bonora E., Pennisi L.F., Toller M., Iommarini L., Ghelli A., Moretti M., Betts C.M., Martinelli G.N., Ceroni A.R., Curcio F., Carelli V., Rugolo M., Tallini G., Romeo G. Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:9001-9006.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 9001-9006
-
-
Gasparre, G.1
Porcelli, A.M.2
Bonora, E.3
Pennisi, L.F.4
Toller, M.5
Iommarini, L.6
Ghelli, A.7
Moretti, M.8
Betts, C.M.9
Martinelli, G.N.10
Ceroni, A.R.11
Curcio, F.12
Carelli, V.13
Rugolo, M.14
Tallini, G.15
Romeo, G.16
-
9
-
-
44849109318
-
Specificity of mtDNA-directed PCR-influence of NUclear MTDNA insertion (NUMT) contamination in routine samples and techniques
-
Goios A., Prieto L., Amorim A., Pereira L. Specificity of mtDNA-directed PCR-influence of NUclear MTDNA insertion (NUMT) contamination in routine samples and techniques. Int. J. Legal Med. 2008, 122:341-345.
-
(2008)
Int. J. Legal Med.
, vol.122
, pp. 341-345
-
-
Goios, A.1
Prieto, L.2
Amorim, A.3
Pereira, L.4
-
10
-
-
10844287252
-
Transfer of a mitochondrial DNA fragment to MCOLN1 causes an inherited case of mucolipidosis IV
-
Goldin E., Stahl S., Cooney A.M., Kaneski C.R., Gupta S., Brady R.O., Ellis J.R., Schiffmann R. Transfer of a mitochondrial DNA fragment to MCOLN1 causes an inherited case of mucolipidosis IV. Hum. Mutat. 2004, 24:460-465.
-
(2004)
Hum. Mutat.
, vol.24
, pp. 460-465
-
-
Goldin, E.1
Stahl, S.2
Cooney, A.M.3
Kaneski, C.R.4
Gupta, S.5
Brady, R.O.6
Ellis, J.R.7
Schiffmann, R.8
-
11
-
-
0032729633
-
Mitochondrial gene mutation, but not large-scale deletion, is a feature of colorectal carcinomas with mitochondrial microsatellite instability
-
Habano W., Sugai T., Yoshida T., Nakamura S. Mitochondrial gene mutation, but not large-scale deletion, is a feature of colorectal carcinomas with mitochondrial microsatellite instability. Int. J. Cancer 1999, 83:625-629.
-
(1999)
Int. J. Cancer
, vol.83
, pp. 625-629
-
-
Habano, W.1
Sugai, T.2
Yoshida, T.3
Nakamura, S.4
-
12
-
-
70349895392
-
Mitochondrial insertions into primate nuclear genomes suggest the use of numts as a tool for phylogeny
-
Hazkani-Covo E. Mitochondrial insertions into primate nuclear genomes suggest the use of numts as a tool for phylogeny. Mol. Biol. Evol. 2009, 26:2175-2179.
-
(2009)
Mol. Biol. Evol.
, vol.26
, pp. 2175-2179
-
-
Hazkani-Covo, E.1
-
13
-
-
55449085777
-
Numt-mediated double-strand break repair mitigates deletions during primate genome evolution
-
Hazkani-Covo E., Covo S. Numt-mediated double-strand break repair mitigates deletions during primate genome evolution. PLoS Genet. 2008, 4:e1000237.
-
(2008)
PLoS Genet.
, vol.4
-
-
Hazkani-Covo, E.1
Covo, S.2
-
14
-
-
33845907665
-
A comparative analysis of numt evolution in human and chimpanzee
-
Hazkani-Covo E., Graur D. A comparative analysis of numt evolution in human and chimpanzee. Mol. Biol. Evol. 2007, 24:13-18.
-
(2007)
Mol. Biol. Evol.
, vol.24
, pp. 13-18
-
-
Hazkani-Covo, E.1
Graur, D.2
-
15
-
-
0037309706
-
Evolutionary dynamics of large numts in the human genome: rarity of independent insertions and abundance of post-insertion duplications
-
Hazkani-Covo E., Sorek R., Graur D. Evolutionary dynamics of large numts in the human genome: rarity of independent insertions and abundance of post-insertion duplications. J. Mol. Evol. 2003, 56:169-174.
-
(2003)
J. Mol. Evol.
, vol.56
, pp. 169-174
-
-
Hazkani-Covo, E.1
Sorek, R.2
Graur, D.3
-
16
-
-
77649210966
-
Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes
-
Hazkani-Covo E., Zeller R.M., Martin W. Molecular poltergeists: mitochondrial DNA copies (numts) in sequenced nuclear genomes. PLoS Genet. 2010, 6:e1000834.
-
(2010)
PLoS Genet.
, vol.6
-
-
Hazkani-Covo, E.1
Zeller, R.M.2
Martin, W.3
-
17
-
-
33745034691
-
Mitochondrial disorders in renal tumors
-
Hervouet E., Godinot C. Mitochondrial disorders in renal tumors. Mitochondrion 2006, 6:105-117.
-
(2006)
Mitochondrion
, vol.6
, pp. 105-117
-
-
Hervouet, E.1
Godinot, C.2
-
19
-
-
34548127859
-
Relationship between mitochondrial DNA mutations and clinical characteristics in human lung cancer
-
Jin X., Zhang J., Gao Y., Ding K., Wang N., Zhou D., Jen J., Cheng S. Relationship between mitochondrial DNA mutations and clinical characteristics in human lung cancer. Mitochondrion 2007, 7:347-353.
-
(2007)
Mitochondrion
, vol.7
, pp. 347-353
-
-
Jin, X.1
Zhang, J.2
Gao, Y.3
Ding, K.4
Wang, N.5
Zhou, D.6
Jen, J.7
Cheng, S.8
-
20
-
-
0035866352
-
Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations
-
Jones J.B., Song J.J., Hempen P.M., Parmigiani G., Hruban R.H., Kern S.E. Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations. Cancer Res. 2001, 61:1299-1304.
-
(2001)
Cancer Res.
, vol.61
, pp. 1299-1304
-
-
Jones, J.B.1
Song, J.J.2
Hempen, P.M.3
Parmigiani, G.4
Hruban, R.H.5
Kern, S.E.6
-
21
-
-
35348857507
-
Mitochondrial DNA mutations in pancreatic cancer
-
Kassauei K., Habbe N., Mullendore M.E., Karikari C.A., Maitra A., Feldmann G. Mitochondrial DNA mutations in pancreatic cancer. Int. J. Gastrointest. Cancer 2006, 37:57-64.
-
(2006)
Int. J. Gastrointest. Cancer
, vol.37
, pp. 57-64
-
-
Kassauei, K.1
Habbe, N.2
Mullendore, M.E.3
Karikari, C.A.4
Maitra, A.5
Feldmann, G.6
-
22
-
-
66449102561
-
DNA transfer from organelles to the nucleus: the idiosyncratic genetics of endosymbiosis
-
Kleine T., Maier U.G., Leister D. DNA transfer from organelles to the nucleus: the idiosyncratic genetics of endosymbiosis. Annu. Rev. Plant Biol. 2009, 60:115-138.
-
(2009)
Annu. Rev. Plant Biol.
, vol.60
, pp. 115-138
-
-
Kleine, T.1
Maier, U.G.2
Leister, D.3
-
23
-
-
47249160395
-
The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS
-
Lascaro D., Castellana S., Gasparre G., Romeo G., Saccone C., Attimonelli M. The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS. BMC Genomics 2008, 9:267.
-
(2008)
BMC Genomics
, vol.9
, pp. 267
-
-
Lascaro, D.1
Castellana, S.2
Gasparre, G.3
Romeo, G.4
Saccone, C.5
Attimonelli, M.6
-
24
-
-
27744526687
-
Origin, evolution and genetic effects of nuclear insertions of organelle DNA
-
Leister D. Origin, evolution and genetic effects of nuclear insertions of organelle DNA. Trends Genet. 2005, 21:655-663.
-
(2005)
Trends Genet.
, vol.21
, pp. 655-663
-
-
Leister, D.1
-
25
-
-
20644445442
-
Clinical value of mitochondrial mutations in colorectal cancer
-
Lievre A., Chapusot C., Bouvier A.M., Zinzindohoue F., Piard F., Roignot P., Arnould L., Beaune P., Faivre J., Laurent-Puig P. Clinical value of mitochondrial mutations in colorectal cancer. J. Clin. Oncol. 2005, 23:3517-3525.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 3517-3525
-
-
Lievre, A.1
Chapusot, C.2
Bouvier, A.M.3
Zinzindohoue, F.4
Piard, F.5
Roignot, P.6
Arnould, L.7
Beaune, P.8
Faivre, J.9
Laurent-Puig, P.10
-
26
-
-
0035882029
-
High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas
-
Liu V.W., Shi H.H., Cheung A.N., Chiu P.M., Leung T.W., Nagley P., Wong L.C., Ngan H.Y. High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas. Cancer Res. 2001, 61:5998-6001.
-
(2001)
Cancer Res.
, vol.61
, pp. 5998-6001
-
-
Liu, V.W.1
Shi, H.H.2
Cheung, A.N.3
Chiu, P.M.4
Leung, T.W.5
Nagley, P.6
Wong, L.C.7
Ngan, H.Y.8
-
27
-
-
0141433448
-
Homoplasmic MELAS A3243G mtDNA mutation in a colon cancer sample
-
Lorenc A., Bryk J., Golik P., Kupryjanczyk J., Ostrowski J., Pronicki M., Semczuk A., Szolkowska M., Bartnik E. Homoplasmic MELAS A3243G mtDNA mutation in a colon cancer sample. Mitochondrion 2003, 3:119-124.
-
(2003)
Mitochondrion
, vol.3
, pp. 119-124
-
-
Lorenc, A.1
Bryk, J.2
Golik, P.3
Kupryjanczyk, J.4
Ostrowski, J.5
Pronicki, M.6
Semczuk, A.7
Szolkowska, M.8
Bartnik, E.9
-
28
-
-
1042299965
-
Mitochondrial DNA-like sequences in the nucleus (NUMTs): insights into our African origins and the mechanism of foreign DNA integration
-
Mishmar D., Ruiz-Pesini E., Brandon M., Wallace D.C. Mitochondrial DNA-like sequences in the nucleus (NUMTs): insights into our African origins and the mechanism of foreign DNA integration. Hum. Mutat. 2004, 23:125-133.
-
(2004)
Hum. Mutat.
, vol.23
, pp. 125-133
-
-
Mishmar, D.1
Ruiz-Pesini, E.2
Brandon, M.3
Wallace, D.C.4
-
29
-
-
34547699355
-
Mitochondrial mutations are a late event in the progression of head and neck squamous cell cancer
-
Mithani S.K., Taube J.M., Zhou S., Smith I.M., Koch W.M., Westra W.H., Califano J.A. Mitochondrial mutations are a late event in the progression of head and neck squamous cell cancer. Clin. Cancer Res. 2007, 13:4331-4335.
-
(2007)
Clin. Cancer Res.
, vol.13
, pp. 4331-4335
-
-
Mithani, S.K.1
Taube, J.M.2
Zhou, S.3
Smith, I.M.4
Koch, W.M.5
Westra, W.H.6
Califano, J.A.7
-
30
-
-
0037314430
-
Mutations of mtDNA in renal cell tumours arising in end-stage renal disease
-
Nagy A., Wilhelm M., Kovacs G. Mutations of mtDNA in renal cell tumours arising in end-stage renal disease. J. Pathol. 2003, 199:237-242.
-
(2003)
J. Pathol.
, vol.199
, pp. 237-242
-
-
Nagy, A.1
Wilhelm, M.2
Kovacs, G.3
-
31
-
-
0032499526
-
Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations
-
Parfait B., Rustin P., Munnich A., Rotig A. Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations. Biochem. Biophys. Res. Commun. 1998, 247:57-59.
-
(1998)
Biochem. Biophys. Res. Commun.
, vol.247
, pp. 57-59
-
-
Parfait, B.1
Rustin, P.2
Munnich, A.3
Rotig, A.4
-
32
-
-
33745984239
-
Somatic mitochondrial DNA mutations in prostate cancer and normal appearing adjacent glands in comparison to age-matched prostate samples without malignant histology
-
Parr R.L., Dakubo G.D., Crandall K.A., Maki J., Reguly B., Aguirre A., Wittock R., Robinson K., Alexander J.S., Birch-Machin M.A., Abdel-Malak M., Froberg M.K., Diamandis E.P., Thayer R.E. Somatic mitochondrial DNA mutations in prostate cancer and normal appearing adjacent glands in comparison to age-matched prostate samples without malignant histology. J. Mol. Diagn. 2006, 8:312-319.
-
(2006)
J. Mol. Diagn.
, vol.8
, pp. 312-319
-
-
Parr, R.L.1
Dakubo, G.D.2
Crandall, K.A.3
Maki, J.4
Reguly, B.5
Aguirre, A.6
Wittock, R.7
Robinson, K.8
Alexander, J.S.9
Birch-Machin, M.A.10
Abdel-Malak, M.11
Froberg, M.K.12
Diamandis, E.P.13
Thayer, R.E.14
-
33
-
-
33747133231
-
The pseudo-mitochondrial genome influences mistakes in heteroplasmy interpretation
-
Parr R.L., Maki J., Reguly B., Dakubo G.D., Aguirre A., Wittock R., Robinson K., Jakupciak J.P., Thayer R.E. The pseudo-mitochondrial genome influences mistakes in heteroplasmy interpretation. BMC Genomics 2006, 7:185.
-
(2006)
BMC Genomics
, vol.7
, pp. 185
-
-
Parr, R.L.1
Maki, J.2
Reguly, B.3
Dakubo, G.D.4
Aguirre, A.5
Wittock, R.6
Robinson, K.7
Jakupciak, J.P.8
Thayer, R.E.9
-
34
-
-
0035886843
-
Detection of mitochondrial DNA mutations in primary breast cancer and fine-needle aspirates
-
Parrella P., Xiao Y., Fliss M., Sanchez-Cespedes M., Mazzarelli P., Rinaldi M., Nicol T., Gabrielson E., Cuomo C., Cohen D., Pandit S., Spencer M., Rabitti C., Fazio V.M., Sidransky D. Detection of mitochondrial DNA mutations in primary breast cancer and fine-needle aspirates. Cancer Res. 2001, 61:7623-7626.
-
(2001)
Cancer Res.
, vol.61
, pp. 7623-7626
-
-
Parrella, P.1
Xiao, Y.2
Fliss, M.3
Sanchez-Cespedes, M.4
Mazzarelli, P.5
Rinaldi, M.6
Nicol, T.7
Gabrielson, E.8
Cuomo, C.9
Cohen, D.10
Pandit, S.11
Spencer, M.12
Rabitti, C.13
Fazio, V.M.14
Sidransky, D.15
-
35
-
-
20044364344
-
MtDNA mutations increase tumorigenicity in prostate cancer
-
Petros J.A., Baumann A.K., Ruiz-Pesini E., Amin M.B., Sun C.Q., Hall J., Lim S., Issa M.M., Flanders W.D., Hosseini S.H., Marshall F.F., Wallace D.C. mtDNA mutations increase tumorigenicity in prostate cancer. Proc. Natl. Acad. Sci. U.S.A. 2005, 102:719-724.
-
(2005)
Proc. Natl. Acad. Sci. U.S.A.
, vol.102
, pp. 719-724
-
-
Petros, J.A.1
Baumann, A.K.2
Ruiz-Pesini, E.3
Amin, M.B.4
Sun, C.Q.5
Hall, J.6
Lim, S.7
Issa, M.M.8
Flanders, W.D.9
Hosseini, S.H.10
Marshall, F.F.11
Wallace, D.C.12
-
36
-
-
0031736203
-
Somatic mutations of the mitochondrial genome in human colorectal tumours
-
Polyak K., Li Y., Zhu H., Lengauer C., Willson J.K., Markowitz S.D., Trush M.A., Kinzler K.W., Vogelstein B. Somatic mutations of the mitochondrial genome in human colorectal tumours. Nat. Genet. 1998, 20:291-293.
-
(1998)
Nat. Genet.
, vol.20
, pp. 291-293
-
-
Polyak, K.1
Li, Y.2
Zhu, H.3
Lengauer, C.4
Willson, J.K.5
Markowitz, S.D.6
Trush, M.A.7
Kinzler, K.W.8
Vogelstein, B.9
-
37
-
-
69249240129
-
Human mitochondrial DNA complete amplification and sequencing: a new validated primer set that prevents nuclear DNA sequences of mitochondrial origin co-amplification
-
Ramos A., Santos C., Alvarez L., Nogués R., Aluja M.P. Human mitochondrial DNA complete amplification and sequencing: a new validated primer set that prevents nuclear DNA sequences of mitochondrial origin co-amplification. Electrophoresis 2009, 30:1-7.
-
(2009)
Electrophoresis
, vol.30
, pp. 1-7
-
-
Ramos, A.1
Santos, C.2
Alvarez, L.3
Nogués, R.4
Aluja, M.P.5
-
38
-
-
79952778118
-
Validated primer set that prevents nuclear DNA sequences of mitochondrial origin co-amplification: a revision based on the New Human Genome Reference Sequence (GRCh37)
-
Ramos A., Santos C., Barbena E., Mateiu L., Alvarez L., Nogues R., Aluja M.P. Validated primer set that prevents nuclear DNA sequences of mitochondrial origin co-amplification: a revision based on the New Human Genome Reference Sequence (GRCh37). Electrophoresis 2011, 32:782-783.
-
(2011)
Electrophoresis
, vol.32
, pp. 782-783
-
-
Ramos, A.1
Santos, C.2
Barbena, E.3
Mateiu, L.4
Alvarez, L.5
Nogues, R.6
Aluja, M.P.7
-
39
-
-
19344368527
-
Continued colonization of the human genome by mitochondrial DNA
-
Ricchetti M., Tekaia F., Dujon B. Continued colonization of the human genome by mitochondrial DNA. PLoS Biol. 2004, 2:E273.
-
(2004)
PLoS Biol.
, vol.2
-
-
Ricchetti, M.1
Tekaia, F.2
Dujon, B.3
-
40
-
-
2442637641
-
NUMTs in sequenced eukaryotic genomes
-
Richly E., Leister D. NUMTs in sequenced eukaryotic genomes. Mol. Biol. Evol. 2004, 21:1081-1084.
-
(2004)
Mol. Biol. Evol.
, vol.21
, pp. 1081-1084
-
-
Richly, E.1
Leister, D.2
-
41
-
-
23944434487
-
A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics
-
Salas A., Carracedo A., Macaulay V., Richards M., Bandelt H.J. A practical guide to mitochondrial DNA error prevention in clinical, forensic, and population genetics. Biochem. Biophys. Res. Commun. 2005, 335:891-899.
-
(2005)
Biochem. Biophys. Res. Commun.
, vol.335
, pp. 891-899
-
-
Salas, A.1
Carracedo, A.2
Macaulay, V.3
Richards, M.4
Bandelt, H.J.5
-
42
-
-
57849143324
-
Mitochondrial DNA mutations in cancer: a review
-
Santos C., Martínez M., Lima M., Hao Y.-J., Simoes N., Montiel R. Mitochondrial DNA mutations in cancer: a review. Curr. Top. Med. Chem. 2008, 8:1351-1366.
-
(2008)
Curr. Top. Med. Chem.
, vol.8
, pp. 1351-1366
-
-
Santos, C.1
Martínez, M.2
Lima, M.3
Hao, Y.-J.4
Simoes, N.5
Montiel, R.6
-
43
-
-
18644368714
-
The BioPerl toolkit: Perl modules for the life sciences
-
Stajich J., Block D., Boulez K., Brenner S., Chervitz S., Dagdigian C., Fuellen G., Gilbert J., Korf I., Lapp H., Lehväslaiho H., Matsalla C., Mungall C., Osborne B., Pocock M., Schattner P., Senger M., Stein L., Stupka E., Wilkinson M., Birney E. The BioPerl toolkit: Perl modules for the life sciences. Genome Res. 2002, 12:1611-1618.
-
(2002)
Genome Res.
, vol.12
, pp. 1611-1618
-
-
Stajich, J.1
Block, D.2
Boulez, K.3
Brenner, S.4
Chervitz, S.5
Dagdigian, C.6
Fuellen, G.7
Gilbert, J.8
Korf, I.9
Lapp, H.10
Lehväslaiho, H.11
Matsalla, C.12
Mungall, C.13
Osborne, B.14
Pocock, M.15
Schattner, P.16
Senger, M.17
Stein, L.18
Stupka, E.19
Wilkinson, M.20
Birney, E.21
more..
-
44
-
-
33646559185
-
Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer
-
Tan D.J., Chang J., Liu L.L., Bai R.K., Wang Y.F., Yeh K.T., Wong L.J. Significance of somatic mutations and content alteration of mitochondrial DNA in esophageal cancer. BMC Cancer 2006, 6:93.
-
(2006)
BMC Cancer
, vol.6
, pp. 93
-
-
Tan, D.J.1
Chang, J.2
Liu, L.L.3
Bai, R.K.4
Wang, Y.F.5
Yeh, K.T.6
Wong, L.J.7
-
45
-
-
12444335944
-
Nuclear insertions help and hinder inference of the evolutionary history of gorilla mtDNA
-
Thalmann O., Serre D., Hofreiter M., Lukas D., Eriksson J., Vigilant L. Nuclear insertions help and hinder inference of the evolutionary history of gorilla mtDNA. Mol. Ecol. 2005, 14:179-188.
-
(2005)
Mol. Ecol.
, vol.14
, pp. 179-188
-
-
Thalmann, O.1
Serre, D.2
Hofreiter, M.3
Lukas, D.4
Eriksson, J.5
Vigilant, L.6
-
46
-
-
0036296922
-
Structure and chromosomal distribution of human mitochondrial pseudogenes
-
Tourmen Y., Baris O., Dessen P., Jacques C., Malthiery Y., Reynier P. Structure and chromosomal distribution of human mitochondrial pseudogenes. Genomics 2002, 80:71-77.
-
(2002)
Genomics
, vol.80
, pp. 71-77
-
-
Tourmen, Y.1
Baris, O.2
Dessen, P.3
Jacques, C.4
Malthiery, Y.5
Reynier, P.6
-
47
-
-
0037359926
-
Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer
-
(112, 303-309)
-
Turner C., Killoran C., Thomas N.S.T., Rosenberg M., Chuzhanova N.A., Johnston J., Kemel Y., Cooper D.N., Biesecker L.G. Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer. Hum. Genet. 2003, 112:303-309. (112, 303-309).
-
(2003)
Hum. Genet.
, vol.112
, pp. 303-309
-
-
Turner, C.1
Killoran, C.2
Thomas, N.S.T.3
Rosenberg, M.4
Chuzhanova, N.A.5
Johnston, J.6
Kemel, Y.7
Cooper, D.N.8
Biesecker, L.G.9
-
48
-
-
34248655678
-
ND4 mutation in transitional cell carcinoma: does mitochondrial mutation occur before tumorigenesis?
-
Tzen C.Y., Mau B.L., Wu T.Y. ND4 mutation in transitional cell carcinoma: does mitochondrial mutation occur before tumorigenesis?. Mitochondrion 2007, 7:273-278.
-
(2007)
Mitochondrion
, vol.7
, pp. 273-278
-
-
Tzen, C.Y.1
Mau, B.L.2
Wu, T.Y.3
-
49
-
-
64049089255
-
Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation
-
Van Oven M., Kayser M. Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation. Hum. Mutat. 2009, 30:E386-E394.
-
(2009)
Hum. Mutat.
, vol.30
-
-
Van Oven, M.1
Kayser, M.2
-
50
-
-
0036073133
-
Pattern of organization of human mitochondrial pseudogenes in the nuclear genome
-
Woischnik M., Moraes C.T. Pattern of organization of human mitochondrial pseudogenes in the nuclear genome. Genome Res. 2002, 12:885-893.
-
(2002)
Genome Res.
, vol.12
, pp. 885-893
-
-
Woischnik, M.1
Moraes, C.T.2
-
51
-
-
1842614835
-
A call for mtDNA data quality control in forensic science
-
Yao Y.G., Bravi C.M., Bandelt H.J. A call for mtDNA data quality control in forensic science. Forensic Sci. Int. 2004, 141:1-6.
-
(2004)
Forensic Sci. Int.
, vol.141
, pp. 1-6
-
-
Yao, Y.G.1
Bravi, C.M.2
Bandelt, H.J.3
-
52
-
-
56649112226
-
Pseudomitochondrial genome haunts disease studies
-
Yao Y.G., Kong Q.P., Salas A., Bandelt H.J. Pseudomitochondrial genome haunts disease studies. J. Med. Genet. 2008, 45:769-772.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 769-772
-
-
Yao, Y.G.1
Kong, Q.P.2
Salas, A.3
Bandelt, H.J.4
-
53
-
-
34250624498
-
Frequency and phenotypic implications of mitochondrial DNA mutations in human squamous cell cancers of the head and neck
-
Zhou S., Kachhap S., Sun W., Wu G., Chuang A., Poeta L., Grumbine L., Mithani S.K., Chatterjee A., Koch W., Westra W.H., Maitra A., Glazer C., Carducci M., Sidransky D., McFate T., Verma A., Califano J.A. Frequency and phenotypic implications of mitochondrial DNA mutations in human squamous cell cancers of the head and neck. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:7540-7545.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 7540-7545
-
-
Zhou, S.1
Kachhap, S.2
Sun, W.3
Wu, G.4
Chuang, A.5
Poeta, L.6
Grumbine, L.7
Mithani, S.K.8
Chatterjee, A.9
Koch, W.10
Westra, W.H.11
Maitra, A.12
Glazer, C.13
Carducci, M.14
Sidransky, D.15
McFate, T.16
Verma, A.17
Califano, J.A.18
|