-
1
-
-
34250355048
-
Mitochondrial genetic background modifies breast cancer risk
-
Bai R.K., Leal S.M., Covarrubias D., Liu A., Wong L.J. Mitochondrial genetic background modifies breast cancer risk. Cancer Res. 2007, 67(10):4687-4694.
-
(2007)
Cancer Res.
, vol.67
, Issue.10
, pp. 4687-4694
-
-
Bai, R.K.1
Leal, S.M.2
Covarrubias, D.3
Liu, A.4
Wong, L.J.5
-
2
-
-
24744442376
-
Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women
-
Canter J.A., Kallianpur A.R., Parl F.F., Millikan R.C. Mitochondrial DNA G10398A polymorphism and invasive breast cancer in African-American women. Cancer Res. 2005, 65(17):8028-8033.
-
(2005)
Cancer Res.
, vol.65
, Issue.17
, pp. 8028-8033
-
-
Canter, J.A.1
Kallianpur, A.R.2
Parl, F.F.3
Millikan, R.C.4
-
3
-
-
77953023689
-
Mitochondrial NADH-dehydrogenase subunit 3 (ND3) polymorphism (A10398G) and sporadic breast cancer in Poland
-
Czarnecka A.M., Krawczyk T., Zdrozny M., Lubinski J., Arnold R.S., Kukwa W., Scinska A., Golik P., Bartnik E., Petros J.A. Mitochondrial NADH-dehydrogenase subunit 3 (ND3) polymorphism (A10398G) and sporadic breast cancer in Poland. Breast Cancer Res. Treat. 2009, 34:45-56.
-
(2009)
Breast Cancer Res. Treat.
, vol.34
, pp. 45-56
-
-
Czarnecka, A.M.1
Krawczyk, T.2
Zdrozny, M.3
Lubinski, J.4
Arnold, R.S.5
Kukwa, W.6
Scinska, A.7
Golik, P.8
Bartnik, E.9
Petros, J.A.10
-
4
-
-
35648979576
-
Increased risk of oral cancer in relation to common Indian mitochondrial polymorphisms and autosomal GSTP1 locus
-
Datta S., Majumder M., Biswas N.K., Sikdar N., Roy B. Increased risk of oral cancer in relation to common Indian mitochondrial polymorphisms and autosomal GSTP1 locus. Cancer 2007, 110(9):1991-1999.
-
(2007)
Cancer
, vol.110
, Issue.9
, pp. 1991-1999
-
-
Datta, S.1
Majumder, M.2
Biswas, N.K.3
Sikdar, N.4
Roy, B.5
-
5
-
-
0037972522
-
Mitochondrial respiratory-chain diseases
-
DiMauro S., Schon E.A. Mitochondrial respiratory-chain diseases. New Engl. J. Med. 2003, 348(26):2656-2668.
-
(2003)
New Engl. J. Med.
, vol.348
, Issue.26
, pp. 2656-2668
-
-
DiMauro, S.1
Schon, E.A.2
-
6
-
-
33846625058
-
Associating mitochondrial DNA variation with complex traits
-
(author reply 382-383)
-
Elson J.L., Majamaa K., Howell N., Chinnery P.F. Associating mitochondrial DNA variation with complex traits. Am. J. Hum. Genet. 2007, 80(2):378-382. (author reply 382-383).
-
(2007)
Am. J. Hum. Genet.
, vol.80
, Issue.2
, pp. 378-382
-
-
Elson, J.L.1
Majamaa, K.2
Howell, N.3
Chinnery, P.F.4
-
7
-
-
33847191391
-
Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians
-
Fuku N., Park K.S., Yamada Y., Nishigaki Y., Cho Y.M., Matsuo H., Segawa T., Watanabe S., Kato K., Yokoi K., Nozawa Y., Lee H.K., Tanaka M. Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians. Am. J. Hum. Genet. 2007, 80(3):407-415.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, Issue.3
, pp. 407-415
-
-
Fuku, N.1
Park, K.S.2
Yamada, Y.3
Nishigaki, Y.4
Cho, Y.M.5
Matsuo, H.6
Segawa, T.7
Watanabe, S.8
Kato, K.9
Yokoi, K.10
Nozawa, Y.11
Lee, H.K.12
Tanaka, M.13
-
8
-
-
0034682803
-
Mitochondria shape hormonally induced cytoplasmic calcium oscillations and modulate exocytosis
-
Kaftan E.J., Xu T., Abercrombie R.F., Hille B. Mitochondria shape hormonally induced cytoplasmic calcium oscillations and modulate exocytosis. J. Biol. Chem. 2000, 275(33):25465-25470.
-
(2000)
J. Biol. Chem.
, vol.275
, Issue.33
, pp. 25465-25470
-
-
Kaftan, E.J.1
Xu, T.2
Abercrombie, R.F.3
Hille, B.4
-
9
-
-
33748087125
-
Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics
-
Kazuno A.A., Munakata K., Nagai T., Shimozono S., Tanaka M., Yoneda M., Kato N., Miyawaki A., Kato T. Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamics. PLoS Genet. 2006, 2(8):e128.
-
(2006)
PLoS Genet.
, vol.2
, Issue.8
-
-
Kazuno, A.A.1
Munakata, K.2
Nagai, T.3
Shimozono, S.4
Tanaka, M.5
Yoneda, M.6
Kato, N.7
Miyawaki, A.8
Kato, T.9
-
10
-
-
0036360796
-
The prevalence of the mitochondrial DNA 16189 variant in non-diabetic Korean adults and its association with higher fasting glucose and body mass index
-
Kim J.H., Park K.S., Cho Y.M., Kang B.S., Kim S.K., Jeon H.J., Kim S.Y., Lee H.K. The prevalence of the mitochondrial DNA 16189 variant in non-diabetic Korean adults and its association with higher fasting glucose and body mass index. Diabet. Med. 2002, 19(8):681-684.
-
(2002)
Diabet. Med.
, vol.19
, Issue.8
, pp. 681-684
-
-
Kim, J.H.1
Park, K.S.2
Cho, Y.M.3
Kang, B.S.4
Kim, S.K.5
Jeon, H.J.6
Kim, S.Y.7
Lee, H.K.8
-
11
-
-
25444493633
-
High prevalence of hyperuricemia in elderly Taiwanese
-
Lee M.S., Lin S.C., Chang H.Y., Lyu L.C., Tsai K.S., Pan W.H. High prevalence of hyperuricemia in elderly Taiwanese. Asia Pac. J. Clin. Nutr. 2005, 14(3):285-292.
-
(2005)
Asia Pac. J. Clin. Nutr.
, vol.14
, Issue.3
, pp. 285-292
-
-
Lee, M.S.1
Lin, S.C.2
Chang, H.Y.3
Lyu, L.C.4
Tsai, K.S.5
Pan, W.H.6
-
12
-
-
3042561892
-
Prevalence of the metabolic syndrome among 40,698 Korean metropolitan subjects
-
Lee W.Y., Park J.S., Noh S.Y., Rhee E.J., Kim S.W., Zimmet P.Z. Prevalence of the metabolic syndrome among 40,698 Korean metropolitan subjects. Diabet. Res. Clin. Pract. 2004, 65(2):143-149.
-
(2004)
Diabet. Res. Clin. Pract.
, vol.65
, Issue.2
, pp. 143-149
-
-
Lee, W.Y.1
Park, J.S.2
Noh, S.Y.3
Rhee, E.J.4
Kim, S.W.5
Zimmet, P.Z.6
-
13
-
-
0032486118
-
Yield of mtDNA mutation analysis in 2000 patients
-
Liang M.H., Wong L.J. Yield of mtDNA mutation analysis in 2000 patients. Am. J. Med. Genet. 1998, 77(5):395-400.
-
(1998)
Am. J. Med. Genet.
, vol.77
, Issue.5
, pp. 395-400
-
-
Liang, M.H.1
Wong, L.J.2
-
14
-
-
54749151061
-
Novel mutations of mitochondrial DNA associated with type 2 diabetes in Chinese Han population
-
Liao W.Q., Pang Y., Yu C.A., Wen J.Y., Zhang Y.G., Li X.H. Novel mutations of mitochondrial DNA associated with type 2 diabetes in Chinese Han population. Tohoku J. Exp. Med. 2008, 215(4):377-384.
-
(2008)
Tohoku J. Exp. Med.
, vol.215
, Issue.4
, pp. 377-384
-
-
Liao, W.Q.1
Pang, Y.2
Yu, C.A.3
Wen, J.Y.4
Zhang, Y.G.5
Li, X.H.6
-
15
-
-
54249156545
-
Metabolic syndrome: from epidemiology to systems biology
-
Lusis A.J., Attie A.D., Reue K. Metabolic syndrome: from epidemiology to systems biology. Nat. Rev. Genet. 2008, 9(11):819-830.
-
(2008)
Nat. Rev. Genet.
, vol.9
, Issue.11
, pp. 819-830
-
-
Lusis, A.J.1
Attie, A.D.2
Reue, K.3
-
16
-
-
0038054341
-
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
-
Mootha V.K., Lindgren C.M., Eriksson K.F., Subramanian A., Sihag S., Lehar J., Puigserver P., Carlsson E., Ridderstrale M., Laurila E., Houstis N., Daly M.J., Patterson N., Mesirov J.P., Golub T.R., Tamayo P., Spiegelman B., Lander E.S., Hirschhorn J.N., Altshuler D., Groop L.C. PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nat. Genet. 2003, 34(3):267-273.
-
(2003)
Nat. Genet.
, vol.34
, Issue.3
, pp. 267-273
-
-
Mootha, V.K.1
Lindgren, C.M.2
Eriksson, K.F.3
Subramanian, A.4
Sihag, S.5
Lehar, J.6
Puigserver, P.7
Carlsson, E.8
Ridderstrale, M.9
Laurila, E.10
Houstis, N.11
Daly, M.J.12
Patterson, N.13
Mesirov, J.P.14
Golub, T.R.15
Tamayo, P.16
Spiegelman, B.17
Lander, E.S.18
Hirschhorn, J.N.19
Altshuler, D.20
Groop, L.C.21
more..
-
17
-
-
34047160902
-
Metabolic syndrome and mitochondrial function: molecular replacement and antioxidant supplements to prevent membrane peroxidation and restore mitochondrial function
-
Nicolson G.L. Metabolic syndrome and mitochondrial function: molecular replacement and antioxidant supplements to prevent membrane peroxidation and restore mitochondrial function. J. Cell Biochem. 2007, 100(6):1352-1369.
-
(2007)
J. Cell Biochem.
, vol.100
, Issue.6
, pp. 1352-1369
-
-
Nicolson, G.L.1
-
18
-
-
5644243261
-
Mitochondrial polymporphisms in Parkinson's disease
-
Otaegui D., Paisan C., Saenz A., Marti I., Ribate M., Marti-Masso J.F., Perez-Tur J., Lopez de Munain A. Mitochondrial polymporphisms in Parkinson's disease. Neurosci. Lett. 2004, 370(2-3):171-174.
-
(2004)
Neurosci. Lett.
, vol.370
, Issue.2-3
, pp. 171-174
-
-
Otaegui, D.1
Paisan, C.2
Saenz, A.3
Marti, I.4
Ribate, M.5
Marti-Masso, J.F.6
Perez-Tur, J.7
Lopez de Munain, A.8
-
19
-
-
65449143954
-
The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk
-
Pezzotti A., Kraft P., Hankinson S.E., Hunter D.J., Buring J., Cox D.G. The mitochondrial A10398G polymorphism, interaction with alcohol consumption, and breast cancer risk. PLoS One 2009, 4(4):e5356.
-
(2009)
PLoS One
, vol.4
, Issue.4
-
-
Pezzotti, A.1
Kraft, P.2
Hankinson, S.E.3
Hunter, D.J.4
Buring, J.5
Cox, D.G.6
-
20
-
-
0037096760
-
Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study
-
Poulton J., Luan J., Macaulay V., Hennings S., Mitchell J., Wareham N.J. Type 2 diabetes is associated with a common mitochondrial variant: evidence from a population-based case-control study. Hum. Mol. Genet. 2002, 11(13):1581-1583.
-
(2002)
Hum. Mol. Genet.
, vol.11
, Issue.13
, pp. 1581-1583
-
-
Poulton, J.1
Luan, J.2
Macaulay, V.3
Hennings, S.4
Mitchell, J.5
Wareham, N.J.6
-
21
-
-
0024160877
-
Banting lecture 1988. Role of insulin resistance in human disease
-
Reaven G.M. Banting lecture 1988. Role of insulin resistance in human disease. Diabetes 1988, 37(12):1595-1607.
-
(1988)
Diabetes
, vol.37
, Issue.12
, pp. 1595-1607
-
-
Reaven, G.M.1
-
22
-
-
0032490099
-
Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect
-
Robinson B.H. Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect. Biochim. Biophys. Acta 1998, 1364(2):271-286.
-
(1998)
Biochim. Biophys. Acta
, vol.1364
, Issue.2
, pp. 271-286
-
-
Robinson, B.H.1
-
23
-
-
1842587584
-
Polymorphism, heteroplasmy, mitochondrial fusion and diabetes
-
Sato A., Endo H., Umetsu K., Sone H., Yanagisawa Y., Saigusa A., Aita S., Kagawa Y. Polymorphism, heteroplasmy, mitochondrial fusion and diabetes. Biosci. Rep. 2003, 23(5-6):313-337.
-
(2003)
Biosci. Rep.
, vol.23
, Issue.5-6
, pp. 313-337
-
-
Sato, A.1
Endo, H.2
Umetsu, K.3
Sone, H.4
Yanagisawa, Y.5
Saigusa, A.6
Aita, S.7
Kagawa, Y.8
-
24
-
-
33745273048
-
Comprehensive association testing of common mitochondrial DNA variation in metabolic disease
-
Saxena R., de Bakker P.I., Singer K., Mootha V., Burtt N., Hirschhorn J.N., Gaudet D., Isomaa B., Daly M.J., Groop L., Ardlie K.G., Altshuler D. Comprehensive association testing of common mitochondrial DNA variation in metabolic disease. Am. J. Hum. Genet. 2006, 79(1):54-61.
-
(2006)
Am. J. Hum. Genet.
, vol.79
, Issue.1
, pp. 54-61
-
-
Saxena, R.1
de Bakker, P.I.2
Singer, K.3
Mootha, V.4
Burtt, N.5
Hirschhorn, J.N.6
Gaudet, D.7
Isomaa, B.8
Daly, M.J.9
Groop, L.10
Ardlie, K.G.11
Altshuler, D.12
-
25
-
-
33745410626
-
Mitochondrial disease
-
Schapira A.H. Mitochondrial disease. Lancet 2006, 368(9529):70-82.
-
(2006)
Lancet
, vol.368
, Issue.9529
, pp. 70-82
-
-
Schapira, A.H.1
-
26
-
-
38849174376
-
Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women
-
Setiawan V.W., Chu L.H., John E.M., Ding Y.C., Ingles S.A., Bernstein L., Press M.F., Ursin G., Haiman C.A., Neuhausen S.L. Mitochondrial DNA G10398A variant is not associated with breast cancer in African-American women. Cancer Genet. Cytogenet. 2008, 181(1):16-19.
-
(2008)
Cancer Genet. Cytogenet.
, vol.181
, Issue.1
, pp. 16-19
-
-
Setiawan, V.W.1
Chu, L.H.2
John, E.M.3
Ding, Y.C.4
Ingles, S.A.5
Bernstein, L.6
Press, M.F.7
Ursin, G.8
Haiman, C.A.9
Neuhausen, S.L.10
-
27
-
-
0033762782
-
Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes
-
Silva J.P., Kohler M., Graff C., Oldfors A., Magnuson M.A., Berggren P.O., Larsson N.G. Impaired insulin secretion and beta-cell loss in tissue-specific knockout mice with mitochondrial diabetes. Nat. Genet. 2000, 26(3):336-340.
-
(2000)
Nat. Genet.
, vol.26
, Issue.3
, pp. 336-340
-
-
Silva, J.P.1
Kohler, M.2
Graff, C.3
Oldfors, A.4
Magnuson, M.A.5
Berggren, P.O.6
Larsson, N.G.7
-
28
-
-
0033358590
-
Human mitochondrial complex I in health and disease
-
Smeitink J., van den Heuvel L. Human mitochondrial complex I in health and disease. Am. J. Hum. Genet. 1999, 64(6):1505-1510.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, Issue.6
, pp. 1505-1510
-
-
Smeitink, J.1
van den Heuvel, L.2
-
29
-
-
0029966749
-
Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line, MIN6
-
Soejima A., Inoue K., Takai D., Kaneko M., Ishihara H., Oka Y., Hayashi J.I. Mitochondrial DNA is required for regulation of glucose-stimulated insulin secretion in a mouse pancreatic beta cell line, MIN6. J. Biol. Chem. 1996, 271(42):26194-26199.
-
(1996)
J. Biol. Chem.
, vol.271
, Issue.42
, pp. 26194-26199
-
-
Soejima, A.1
Inoue, K.2
Takai, D.3
Kaneko, M.4
Ishihara, H.5
Oka, Y.6
Hayashi, J.I.7
-
30
-
-
33847048982
-
Women with mitochondrial haplogroup N9a are protected against metabolic syndrome
-
Tanaka M., Fuku N., Nishigaki Y., Matsuo H., Segawa T., Watanabe S., Kato K., Yokoi K., Ito M., Nozawa Y., Yamada Y. Women with mitochondrial haplogroup N9a are protected against metabolic syndrome. Diabetes 2007, 56(2):518-521.
-
(2007)
Diabetes
, vol.56
, Issue.2
, pp. 518-521
-
-
Tanaka, M.1
Fuku, N.2
Nishigaki, Y.3
Matsuo, H.4
Segawa, T.5
Watanabe, S.6
Kato, K.7
Yokoi, K.8
Ito, M.9
Nozawa, Y.10
Yamada, Y.11
-
31
-
-
0037385480
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
-
van der Walt J.M., Nicodemus K.K., Martin E.R., Scott W.K., Nance M.A., Watts R.L., Hubble J.P., Haines J.L., Koller W.C., Lyons K., Pahwa R., Stern M.B., Colcher A., Hiner B.C., Jankovic J., Ondo W.G., Allen F.H., Goetz C.G., Small G.W., Mastaglia F., Stajich J.M., McLaurin A.C., Middleton L.T., Scott B.L., Schmechel D.E., Pericak-Vance M.A., Vance J.M. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. Am. J. Hum. Genet. 2003, 72(4):804-811.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, Issue.4
, pp. 804-811
-
-
van der Walt, J.M.1
Nicodemus, K.K.2
Martin, E.R.3
Scott, W.K.4
Nance, M.A.5
Watts, R.L.6
Hubble, J.P.7
Haines, J.L.8
Koller, W.C.9
Lyons, K.10
Pahwa, R.11
Stern, M.B.12
Colcher, A.13
Hiner, B.C.14
Jankovic, J.15
Ondo, W.G.16
Allen, F.H.17
Goetz, C.G.18
Small, G.W.19
Mastaglia, F.20
Stajich, J.M.21
McLaurin, A.C.22
Middleton, L.T.23
Scott, B.L.24
Schmechel, D.E.25
Pericak-Vance, M.A.26
Vance, J.M.27
more..
-
32
-
-
34447498590
-
Mitochondrial genetic polymorphisms and pancreatic cancer risk
-
Wang L., Bamlet W.R., de Andrade M., Boardman L.A., Cunningham J.M., Thibodeau S.N., Petersen G.M. Mitochondrial genetic polymorphisms and pancreatic cancer risk. Cancer Epidemiol. Biomarkers Prev. 2007, 16(7):1455-1459.
-
(2007)
Cancer Epidemiol. Biomarkers Prev.
, vol.16
, Issue.7
, pp. 1455-1459
-
-
Wang, L.1
Bamlet, W.R.2
de Andrade, M.3
Boardman, L.A.4
Cunningham, J.M.5
Thibodeau, S.N.6
Petersen, G.M.7
-
33
-
-
24344486784
-
Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults
-
Weng S.W., Liou C.W., Lin T.K., Wei Y.H., Lee C.F., Eng H.L., Chen S.D., Liu R.T., Chen J.F., Chen I.Y., Chen M.H., Wang P.W. Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults. J. Clin. Endocrinol. Metab. 2005, 90(9):5037-5040.
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, Issue.9
, pp. 5037-5040
-
-
Weng, S.W.1
Liou, C.W.2
Lin, T.K.3
Wei, Y.H.4
Lee, C.F.5
Eng, H.L.6
Chen, S.D.7
Liu, R.T.8
Chen, J.F.9
Chen, I.Y.10
Chen, M.H.11
Wang, P.W.12
-
34
-
-
0030850573
-
Direct detection of multiple point mutations in mitochondrial DNA
-
Wong L.J., Senadheera D. Direct detection of multiple point mutations in mitochondrial DNA. Clin. Chem. 1997, 43(10):1857-1861.
-
(1997)
Clin. Chem.
, vol.43
, Issue.10
, pp. 1857-1861
-
-
Wong, L.J.1
Senadheera, D.2
|