References of Mitochondrial Interest (Authors M-Z)

Date of last update: 12/1/03. 
This page is part of 
Mitomap: A Human Mitochondrial Genome Database.

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M

Ma, H., Kunes, S., Schatz, P. J. and Botstein, D. (1987). "Plasmid construction by homologous recombination in yeast." Gene 58(2-3):201-216.

Maassen, J. A., van den Ouweland, J. M., tHart, L. M. and Lemkes, H. H. (1997). "Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA." Hormone & Metabolic Research 29(2):50-55.

Maca-Meyer, N., Gonzalez, A.M., Larruga, J.M., Flores, C. and Cabrera, V.M. (2001). "Major genomic mitochondrial lineages delineate early human expansions." BMC Genetics 2(1):13.

Maca-Meyer, N., Sanchez-Velasco, P., Flores, C., Larruga, J. M., Gonzalez, A. M., Oterino, A. and Leyva-Cobian, F. (2003). "Y chromosome and mitochondrial DNA characterization of Pasiegos, a human isolate from Cantabria (Spain)." Annals of Human Genetics 67(4):329-339.

Macaulay, V., Richards, M., Hickey, E., Vega, E., Cruciani, F., Guida, V., Scozzari, R., Bonne-Tamir, B., Sykes, B. and Torroni, A. (1999). "The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs." American Journal of Human Genetics 64(1):232-249.

Macaulay, V. A., Richards, M. B., Forster, P., Bendall, K. E., Watson, E., Sykes, B. and Bandelt, H. J. (1997). "mtDNA mutation rates--no need to panic." American Journal of Human Genetics 61(4):983-990.

MacGregor, R. R. (1987). "Alcohol and drugs as co-factors for AIDS." Advances in Alcohol & Substance Abuse 7(2):47-71.

Macho, A., Castedo, M., Marchetti, P., Aguilar, J. J., Decaudin, D., Zamzami, N., Girard, P. M., Uriel, J. and Kroemer, G. (1995). "Mitochondrial dysfunctions in circulating T lymphocytes from human immunodeficiency virus-1 carriers [see comments]." Blood 86(7):2481-2487.

Mack, S. J. and Erlich, H. A. (1998). "HLA class II polymorphism in the Ticuna of Brazil: evolutionary implications of the DRB10807 allele." Tissue Antigens 51(1):41-50.

Mackey, D. and Howell, N. (1992). "A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology." American Journal of Human Genetics 51(6):1218-1228.

Mackey, D. A. (1994). "Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy." Eye 8(Pt 4):431-436.

Mackey, D. A. and Buttery, R. G. (1992). "Leber hereditary optic neuropathy in Australia." Australian and New Zealand Journal of Ophthalmology 20(3):177-184.

Mackey, D. A., Oostra, R. J., Rosenberg, T., Nikoskelainen, E., Bronte-Stewart, J., Poulton, J., Harding, A. E., Govan, G., Bolhuis, P. A. and Norby, S. (1996). "Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy." American Journal of Human Genetics 59(2):481-485.

Macmillan, C., Kirkham, T., Fu, K., Allison, V., Andermann, E., Chitayat, D., Fortier, D., Gans, M., Hare, H., Quercia, N., Zackon, D. and Shoubridge, E. A. (1998). "Pedigree analysis of French Canadian families with 14484 T>C Leber's hereditary optic neuropathy." Neurology 50(2):417-422.

Macmillan, C., Lach, B. and Shoubridge, E. A. (1993). "Variable distribution of mutant mitochondrial DNAs (tRNALeu[3243]) in tissues of symptomatic relatives with MELAS: the role of mitotic segregation." Neurology 43(8):1586-1590.

Macreadie, I. G., Novitski, C. E., Maxwell, R. J., John, U., Ooi, B. G., McMullen, G. L., Lukins, H. B., Linnane, A. W. and Nagley, P. (1983). "Biogenesis of mitochondria: the mitochondrial gene (aap1) coding for mitochondrial ATPase subunit 8 in Saccharomyces cerevisiae." Nucleic Acids Research 11(13):4435-4451.

Madden, J. J., Donahoe, R. M., Zwemer-Collins, J., Shafer, D. A. and Falek, A. (1987). "Binding of naloxone to human T lymphocytes." Biochemical Pharmacology 36(23):4103-4109.

Madden, J. J., Ketelsen, D., Whaley, W. L., Donahoe, R. M. and Oleson, D. (1995). "Mitogenic activation of human T lymphocytes induces a high affinity morphine binding site." Advances in Experimental Medicine and Biology 373:37-40.

Madden, J. J., Whaley, W. L. and Ketelsen, D. (1998). "Opiate binding sites in the cellular immune system: expression and regulation." Journal of Neuroimmunology 83(1-2):57-62.

Madsen, C. S., Ghivizzani, S. C. and Hauswirth, W. W. (1993). "Protein binding to a single termination-associated sequence in the mitochondrial DNA D-loop region." Molecular and Cellular Biology 13(4):2162-2171.

Magnani, M., Fraternale, A., Casabianca, A., Schiavano, G. F., Chiarantini, L., Palamara, A. T., Ciriolo, M. R., Rotilio, G. and Garaci, E. (1997). "Antiretroviral effect of combined zidovudine and reduced glutathione therapy in murine AIDS." AIDS Research and Human Retroviruses 13(13):1093-1099.

Mahapatra, R. K., Mahapatra, D. and Yaden, S. (1987). "Clinical experience with a transdermal nitroglycerin system." Angiology 38(4):277-286.

Majamaa, K., Moilanen, J. S., Uimonen, S., Remes, A. M., Salmela, P. I., Karppa, M., Majamaa-Voltti, K. A., Rusanen, H., Sorri, M., Peuhkurinen, K. J. and Hassinen, I. E. (1998). "Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population." American Journal of Human Genetics 63(2):447-454.

Majamaa, K., Rusanen, H., Remes, A. and Hassinen, I. E. (1997). "Metabolic interventions against complex I deficiency in MELAS syndrome." Molecular & Cellular Biochemistry 174(1-2):291-296.

Majamaa, K., Turkka, J., Karppa, M., Winqvist, S. and Hassinen, I. E. (1997). "The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct." Neurology 49(5):1331-1334.

Majander, A., Finel, M., Savontaus, M. L., Nikoskelainen, E. and Wikstrom, M. (1996). "Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy." European Journal of Biochemistry 239(1):201-207.

Majander, A., Huoponen, K., Savontaus, M. L., Nikoskelainen, E. and Wikstrom, M. (1991). "Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)." FEBS Letters 292(1-2):289-292.

Majander, A., Lamminen, T., Juvonen, V., Aula, P., Nikoskelainen, E., Savontaus, M. L. and Wikstrom, M. (1997). "Mutations in subunit 6 of the F1F0-ATP synthase cause two entirely different diseases." FEBS Letters 412(2):351-354.

Majumder, P. P., Roy, B., Banerjee, S., Chakraborty, M., Dey, B., Mukherjee, N., Roy, M., Thakurta, P. G. and Sil, S. K. (1999). "Human-specific insertion/deletion polymorphisms in Indian populations and their possible evolutionary implications." European Journal of Human Genetics 7(4):435-446.

Mak, S. C., Chi, C. S. and Tsai, C. R. (1998). "Mitochondrial DNA 8993 T > C mutation presenting as juvenile Leigh syndrome with respiratory failure." Journal of Child Neurology 13(7):349-351.

Makela-Bengs, P., Suomalainen, A., Majander, A., Rapola, J., Kalimo, H., Nuutila, A. and Pihko, H. (1995). "Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome." Pediatric Research 37(5):634-639.

Makino, M., Horai, S., Goto, Y. and Nonaka, I. (1998). "Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome." Neuromuscular Disorders 8(3-4):149-151.

Makman, M. H., Dobrenis, K. and Surratt, C. K. (1998). "Properties of mu 3 opiate alkaloid receptors in macrophages, astrocytes, and HL-60 human promyelocytic leukemia cells." Advances in Experimental Medicine and Biology 437:137-148.

Malaisse, W. J. (1994). "The beta cell in NIDDM: giving light to the blind." Diabetologia 37:S36-42.

Malaisse-Lagae, F. and Malaisse, W. J. (1988). "Hexose metabolism in pancreatic islets: regulation of mitochondrial hexokinase binding." Biochemical Medicine and Metabolic Biology 39(1):80-89.

Malcovati, M., Marchetti, T., Zanelli, T. and Tenchini, M. L., Eds. (1991). Flavins and Flavoproteins 1990. Flavins and Flavoproteins 1990. Berlin, Walter de Gruyter & Co.

Malgat, M., Letellier, T., Jouaville, S. L. and Mazat, J. P. (1995). "Value of control theory in the study of cellular metabolism -- biomedical implications." Journal of Biological Systems 3(1):165-175.

Malhi, R. S., Eshleman, J. A., Greenberg, J. A., Weiss, D. A., Schultz Shook, B. A., Kaestle, F. A., Lorenz, J. G., Kemp, B. M., Johnson, J. R. and Smith, D. G. (2002). "The structure of diversity within New World mitochondrial DNA haplogroups: implications for the prehistory of North America." American Journal of Human Genetics 70(4):905-919.

Malyarchuk, B. A. (1997). "[Distribution of mitochondrial DNA markers in the European populations of Eurasia]." Genetika 33(7):986-991.

Malyarchuk, B. A. (1997). "[A mitochondrial portrait of Eastern Slavs]." Genetika 33(1):101-105.

Malyarchuk, B. A. (1997). "[The origin of caucasoid BamHI-3/MspI-4 mitochondrial DNA marker]." Genetika 33(12):1669-1674.

Malyarchuk, B. A. (1997). "[Similarity of geographic distribution of frequencies of p(c) allele of erythrocyte acid phosphatase and BamHI-3/MspI-4 types of mitochondrial DNA in Caucasoid human populations]." Genetika 33(3):393-398.

Malyarchuk, B. A., Grzybowski, T., Derenko, M. V., Czarny, J., Drobnic, K. and Miscicka-Sliwka, D. (2003). "Mitochondrial DNA variability in Bosnians and Slovenians." Annals of Human Genetics 67(5):412-425.

Malyarchuk, B. A., Grzybowski, T., Derenko, M. V., Czarny, J., Wozniak, M. and Miscicka-Sliwka, D. (2002). "Mitochondrial DNA variability in Poles and Russians." Annals of Human Genetics 66(4):261-283.

Man, P. Y., Griffiths, P. G., Brown, D. T., Howell, N., Turnbull, D. M. and Chinnery, P. F. (2003). "The epidemiology of Leber hereditary optic neuropathy in the North East of England." American Journal of Human Genetics 72(2):333-339.

Man, P. Y., Morris, C. M., Zeviani, M., Carrara, F., Turnbull, D. M. and Chinnery, P. F. (2003). "The role of APOE in the phenotypic expression of Leber hereditary optic neuropathy." Journal of Medical Genetics 40(4):e41.

Man, P. Y., Turnbull, D. M. and Chinnery, P. F. (2002). "Leber hereditary optic neuropathy." Journal of Medical Genetics 39(3):162-169.

Mancini, M., Nicholson, D. W., Roy, S., Thornberry, N. A., Peterson, E. P., Casciola-Rosen, L. A. and Rosen, A. (1998). "The caspase-3 precursor has a cytosolic and mitochondrial distribution: implications for apoptotic signaling." Journal of Cell Biology 140(6):1485-1495.

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Mandavilli, B. S., Santos, J. H. and Van Houten, B. (2002). "Mitochondrial DNA repair and aging." Mutation Research 509(1-2):127-151.

Manfredi, G., Bonilla, E., Schon, E. A., DiMauro, S. and Moraes, C. (1994). "A mitochondrial DNA missense mutation in the cytochrome oxidase subunit III gene associated with a progressive encephalopathy." Miami Short Reports 4:17.

Manfredi, G., Fu, J., Ojaimi, J., Sadlock, J. E., Kwong, J. Q., Guy, J. and Schon, E. A. (2002). "Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus." Nature Genetics 30(4):394-399.

Manfredi, G., Gupta, N., Vazquez-Memije, M. E., Sadlock, J. E., Spinazzola, A., De Vivo, D. C. and Schon, E. A. (1999). "Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene." Journal of Biological Chemistry 274(14):9386-9391.

Manfredi, G., Schon, E. A., Bonilla, E., Moraes, C. T., Shanske, S. and DiMauro, S. (1996). "Identification of a mutation in the mitochondrial tRNA(Cys) gene associated with mitochondrial encephalopathy." Human Mutation 7(2):158-163.

Manfredi, G., Schon, E. A., Moraes, C. T., Bonilla, E., Berry, G. T., Sladky, J. T. and DiMauro, S. (1995). "A new mutation associated with MELAS is located in a mitochondrial DNA polipeptide-coding gene." Neuromuscular Disorders 5(5):391-398.

Manfredi, G., Servidei, S., Bonilla, E., Shanske, S., Schon, E. A., DiMauro, S. and Moraes, C. T. (1995). "High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathy." Neurology 45(4):762-768.

Manfredi, G., Thyagarajan, D., Papadopoulou, L. C., Pallotti, F. and Schon, E. A. (1997). "The fate of human sperm-derived mtDNA in somatic cells." American Journal of Human Genetics 61(4):953-960.

Manfredi, G., Vu, T., Bonilla, E., Schon, E. A., DiMauro, S., Arnaudo, E., Zhang, L., Rowland, L. P. and Hirano, M. (1997). "Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?" Annals of Neurology 42(2):180-188.

Mann, V. M., Cooper, J. M., Krige, D., Daniel, S. E., Schapira, A. H. and Marsden, C. D. (1992). "Brain, skeletal muscle and platelet homogenate mitochondrial function in Parkinson's disease." Brain 115(Pt 2):333-342.

Mann, V. M., Cooper, J. M. and Schapira, A. H. V. (1992). "Quantitation of a mitochondrial DNA deletion in Parkinson's disease." FEBS Letters 299(3):218-222.

Manouvrier, S., Rotig, A., Hannebique, G., Gheerbrandt, J. D., Royer-Legrain, G., Munnich, A., Parent, M., Grunfeld, J. P., Largilliere, C., Lombes, A. and Bonnefont, J. P. (1995). "Point mutation of the mitochondrial tRNALeu gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness." Journal of Medical Genetics 32(8):654-656.

Mansergh, F. C., Millington-Ward, S., Kennan, A., Kiang, A. S., Humphries, M., Farrar, G. J., Humphries, P. and Kenna, P. F. (1999). "Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene." American Journal of Human Genetics 64(4):971-985.

Mansouri, A., Fromenty, B., Berson, A., Robin, M. A., Grimbert, S., Beaugrand, M., Erlinger, S. and Pessayre, D. (1997). "Multiple hepatic mitochondrial DNA deletions suggest premature oxidative aging in alcoholic patients." Journal of Hepatology 27(1):96-102.

Mansouri, A., Gaou, I., Fromenty, B., Berson, A., Letteron, P., Degott, C., Erlinger, S. and Pessayre, D. (1997). "Premature oxidative aging of hepatic mitochondrial DNA in Wilson's disease." Gastroenterology 113(2):599-605.

Mao, M., Fu, G., Wu, J. S., Zhang, Q. H., Zhou, J., Kan, L. X., Huang, Q. H., He, K. L., Gu, B. W., Han, Z. G., Shen, Y., Gu, J., Yu, Y. P., Xu, S. H., Wang, Y. X., Chen, S. J. and Chen, Z. (1998). "Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full- length cDNA cloning." Proceedings of the National Academy of Sciences of the United States of America 95(14):8175-8180.

Marangos, P. J., Patel, J., Boulenger, J. P. and Clark-Rosenberg, R. (1982). "Characterization of peripheral-type benzodiazepine binding sites in brain using [3H]Ro 5-4864." Molecular Pharmacology 22(1):26-32.

Marchington, D. R., Hartshorne, G. M., Barlow, D. and Poulton, J. (1997). "Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck." American Journal of Human Genetics 60(2):408-416.

Marchington, D. R., Macaulay, V., Hartshorne, G. M., Barlow, D. and Poulton, J. (1998). "Evidence from human oocytes for a genetic bottleneck in an mtDNA disease." American Journal of Human Genetics 63(3):769-775.

Marin-Garcia, J., Ananthakrishnan, R. and Goldenthal, M. J. (1995). "Heart mitochondria response to alcohol is different than brain and liver." Alcoholism: Clinical and Experimental Research 19(6):1463-1466.

Marin-Garcia, J., Ananthakrishnan, R. and Goldenthal, M. J. (1996). "Mitochondrial dysfunction after fetal alcohol exposure." Alcoholism: Clinical and Experimental Research 20(6):1029-1032.

Marin-Garcia, J., Ananthakrishnan, R., Goldenthal, M. J., Filiano, J. J. and Perez-Atayde, A. (1997). "Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy." Journal of Inherited Metabolic Disease 20(5):674-680.

Marin-Garcia, J. and Goldenthal, M. J. (1997). "Mitochondrial cardiomyopathy: molecular and biochemical analysis." Pediatric Cardiology 18(4):251-260.

Marin-Garcia, J., Goldenthal, M. J., Flores-Sarnat, L. and Sarnat, H. B. (2002). "Severe mitochondrial cytopathy with complete A-V block, PEO, and mtDNA deletions." Pediatric Neurology 27(3):213-216.

Mariotti, C., Savarese, N., Suomalainen, A., Rimoldi, M., Comi, G., Prelle, A., Antozzi, C., Servidei, S., Jarre, L., DiDonato, S. and Zeviani, M. (1995). "Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA." Journal of Neurology 242(5):304-312.

Mariotti, C., Tiranti, V., Carrara, F., Dallapiccola, B., DiDonato, S. and Zeviani, M. (1994). "Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNALeu(UUR) mutation associated with maternally inherited myopathy and cardiomyopathy." Journal of Clinical Investigation 93(3):1102-1107.

Mariottini, P., Chomyn, A., Attardi, G., Trovato, D., Strong, D. D. and Doolittle, R. F. (1983). "Antibodies against synthetic peptides reveal that the unidentified reading frame A6L, overlapping the ATPase 6 gene, is expressed in human mitochondria." Cell 32(4):1269-1277.

Markel, P., Shu, P., Ebeling, C., Carlson, G. A., Nagle, D. L., Smutko, J. S. and Moore, K. J. (1997). "Theoretical and empirical issues for marker-assisted breeding of congenic mouse strains [see comments]." Nature Genetics 17(3):280-284.

Martin, W. R., Clark, C., Ammann, W., Stoessl, A. J., Shtybel, W. and Hayden, M. R. (1992). "Cortical glucose metabolism in Huntington's disease." Neurology 42(1):223-229.

Martin-Negrier, M. L., Coquet, M., Moretto, B. T., Lacut, J. Y., Dupon, M., Bloch, B., Lestienne, P. and Vital, C. (1998). "Partial triplication of mtDNA in maternally transmitted diabetes mellitus and deafness." American Journal of Human Genetics 63(4):1227-1232.

Marzo, I., Brenner, C., Zamzami, N., Jurgensmeier, J. M., Susin, S. A., Vieira, H. L., Prevost, M. C., Xie, Z., Matsuyama, S., Reed, J. C. and Kroemer, G. (1998). "Bax and adenine nucleotide translocator cooperate in the mitochondrial control of apoptosis." Science 281(5385):2027-2031.

Marzuki, S., Berkovic, S. F., Saifuddin Noer, A., Kapsa, R. M., Kalnins, R. M., Byrne, E., Sasmono, T. and Sudoyo, H. (1997). "Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy." Journal of the Neurological Sciences 145(2):155-162.

Marzuki, S., Lertrit, P., Noer, A. S., Kapsa, R. M. I., Sudoyo, H., Byrne, E. and Thyagarajan, D. (1992). "Reply to Howell etal.: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA." American Journal of Human Genetics 50(6):1337-1340.

Marzuki, S., Noer, A. S., Letrit, P., Thyagarajan, D., Kapsa, R., Utthanaphol, P. and Byrne, E. (1991). "Normal variants of human mitochondrial DNA and translation products: the building of a reference data base." Human Genetics 88(2):139-145.

Mashima, Y., Hiida, Y., Kubota, R., Oguchi, Y., Kudoh, J. and Shimizu, N. (1994). "DNA diagnosis of Leber's hereditary optic neuropathy by using dried blood specimens [letter]." American Journal of Ophthalmology 116(6):773-774.

Mashima, Y., Hiida, Y. and Oguchi, Y. (1992). "Remission of Leber's hereditary optic neuropathy with idebenone [letter]." Lancet 340(8815):368-369.

Mashima, Y., Hiida, Y., Oguchi, Y., Kudoh, J. and Shimizu, N. (1993). "High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy." Human Genetics 92(1):101-102.

Mashima, Y., Hiida, Y., Saga, M., Oguchi, Y., Kudoh, J. and Shimizu, N. (1995). "Risk of false-positive molecular genetic diagnosis of Leber's hereditary optic neuropathy." American Journal of Ophthalmology 119(2):245-246.

Mashima, Y., Saga, M., Hiida, Y., Oguchi, Y., Wakakura, M., Kudoh, J. and Shimizu, N. (1995). "Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism." Investigative Ophthalmology and Visual Science 36(8):1714-1720.

Mashima, Y., Yamada, K., Wakakura, M., Kigasawa, K., Kudoh, J., Shimizu, N. and Oguchi, Y. (1998). "Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy." Current Eye Research 17(4):403-408.

Masoro, E. J. (1993). "Dietary restriction and aging." Journal of the American Geriatrics Society 41(9):994-999.

Masoro, E. J., McCarter, R. J., Katz, M. S. and McMahan, C. A. (1992). "Dietary restriction alters characteristics of glucose fuel use (published erratum appears in J Gerontol 1993 Mar;48(2):B73)." Journal of Gerontology 47(6):B202-B208.

Massin, P., Guillausseau, P. J., Vialettes, B., Paquis, V., Orsini, F., Grimaldi, A. D. and Gaudric, A. (1995). "Macular pattern dystrophy associated with a mutation of mitochondrial DNA." American Journal of Ophthalmology 120(2):247-248.

Massotti, M., Mele, L. and De Luca, C. (1990). "Involvement of the "peripheral" benzodiazepine receptor type (omega 3) in the tolerance to the electroencephalographic effects of benzodiazepines in rats: comparison of diazepam and clonazepam." Pharmacology Biochemsitry and Behavior 35(4):933-936.

Masucci, J. P., Davidson, M., Koga, Y., Schon, E. A. and King, M. P. (1995). "In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNALysgene: two genotypes produce similar phenotypes." Molecular and Cellular Biology 15(5):2872-2881.

Masucci, J. P., Schon, E. A. and King, M. P. (1997). "Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism." Molecular & Cellular Biochemistry 174(1-2):215-219.

Mather, M. W. and Rottenberg, H. (1998). "Intrinsic uncoupling of cytochrome c oxidase may cause the maternally inherited mitochondrial diseases MELAS and LHON." FEBS Letters 433(1-2):93-97.

Mathews, C. E. and Berdanier, C. D. (1998). "Noninsulin-dependent diabetes mellitus as a mitochondrial genomic disease." Proceedings of the Society for Experimental Biology & Medicine 219(2):97-108.

Matouk, C., Gosselin, D., Malo, D., Skamene, E. and Radzioch, D. (1996). "PCR-analyzed microsatellites for the inbred mouse strain 129/Sv, the strain most commonly used in gene knockout technology." Mammalian Genome 7(8):603-605.

Matsuda, C., Endo, H., Ohta, S. and Kagawa, Y. (1993). "Gene structure of human mitochondrial ATP synthase gamma-subunit. Tissue specificity produced by alternative RNA splicing." Journal of Biological Chemistry 268(33):24950-24958.

Matsumoto, M., Hayasaka, S., Hotta, Y., Fujiki, K., Fujimaki, T., Takeda, M., Ishida, N., Endo, S. and Kanai, A. (1998). "Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778." Journal of Human Genetics 43(4):242-245.

Matsumoto, M., Hayasaka, S., Kadoi, C., Hotta, Y., Fujiki, K., Fujimaki, T., Takeda, M., Ishida, N., Endo, S. and Kanai, A. (1999). "Secondary mutations of mitochondrial DNA in Japanese patients with Leber's hereditary optic neuropathy." Ophthalmic Genetics 20(3):153-160.

Matsuya, Y. and Yamane, I. (1985). "Cell fusion and cell agglutination: enhancing effect by a combined use of lectin and polycation." Somatic Cell & Molecular Genetics 11(3):247-255.

Matthews, D. E., Hessler, R. A., Denslow, N. D., Edwards, J. S. and O'Brien, T. W. (1982). "Protein composition of the bovine mitochondrial ribosome." Journal of Biological Chemistry 257(15):8788-8794.

Matthews, P. M., Brown, R. M., Morten, K., Marchington, D., Poulton, J. and Brown, G. (1995). "Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA." Human Genetics 96(3):261-268.

Matthews, P. M., Ford, B., Dandurand, R. J., Eidelman, D. H., O'Connor, D., Sherwin, A., Karpati, G., Andermann, F. and Arnold, D. L. (1993). "Coenzyme Q10 with multiple vitamins is generally ineffective in treatment of mitochondrial disease." Neurology 43(5):884-890.

Matthews, P. M., Hopkin, J., Brown, R. M., Stephenson, J. B., Hilton-Jones, D. and Brown, G. K. (1994). "Comparison of the relative levels of the 3243 (A-G) mtDNA mutation in heteroplasmic adult and fetal tissues." Journal of Medical Genetics 31(1):41-44.

Matthews, P. M., Marchington, D. R., Squier, M., Land, J., Brown, R. M. and Brown, G. K. (1993). "Molecular genetic characterization of an X-linked form of Leigh's syndrome." Annals of Neurology 33(6):652-655.

Matthijs, G., Claes, S., Longo-Mbenza, B. and Cassiman, J. J. (1994). "Teenage onset non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairese pedigree." American Journal of Human Genetics 55:A23 (abstract).

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