US 6596700B2
· Sommadossi
· 2003
[cited by applicant]
EA 005890
· 2005
[cited by applicant]
EP 3302499
· 2018
[cited by applicant]
RU 2300381
· 2007
[cited by applicant]
WO WO20120125848
· 2012
[cited by applicant]
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Saada et al., “Mitochondrial deoxyribonucleotide pools in deoxyguanosine kinase deficiency”, Molecular Genetics and Metabolism. Academic Press. Amsterdam. NL. vol. 95. No. 3. Nov. 1, 2008 (Nov. 1, 2008). pp. 169-173. XP…
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Cowan M J et al: “Deoxycytidine therapy in two patients with adenosine deaminase deficiency and severe immunodeficiency disease”, Clinical Immunology and Immunopathology, San Diego, CA, US, vol. 37, No. 1, Oct. 1, 1985 …
[cited by applicant]
Y. Camara et al: “Administration of deoxyribonucleosides or inhibition of their catabolism as a pharmacological approach for mitochondrial DNA depletion syndrome”, EPO Form 1703 01.91TRI Human Molecular Genetics, vol. 2…
[cited by applicant]
Julia Wang et al: “TK2-Related Mitochondrial DNA Maintenance Defect, Myopathic Form—GeneReviews—NCBI Bookshelf” In: “Gene Reviews”, Dec. 6, 2012 (Dec. 6, 2012), XP055520605.
[cited by applicant]
Steve Perrin: “Make mouse studies work” Nature, vo. 507, p. 423-425, Mar. 27, 2014.
[cited by applicant]
NIH Research Portfolio ONline Reporting Tools (RePORT), project #3—Pharmacological and gene therapy of TK2 deficiency in mice and human, Michio Hirano (accessed Jan. 30, 2018).
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Garone et al., “Deoxypyrimidine monophosphates treatment for thymidine kinase 2 deficiency”, Neurology, suppl. MeetingAbstracts 80.1, 65th American Acadamy of Neurology Annual Meeting, (Feb. 12, 2013), accessed Jan. 30,…
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Akman, Hasan O. “Thymidine kinase 2 (H126N) knockin mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance”, Human Molecular Genetics, May 8, 2008, vol. 17, No. 16, pp. 2433-244…
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Van Goethem, et al. (Jul. 2001) Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. Nature Genet. 28:211-212.
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Akman, et al. (May 6, 2008) Thymidine kinase 2 (H126N) knock in mice show the essential role of balanced deoxynucleotide pools for mitochondrial DNA maintenance. Hum Mol Genet 17:2433-2440.
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Alston, et al. (Dec. 3, 2013) Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions. Neurology. 81:2051-3.
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Bartesaghi, et al. (Jan. 26, 2010) Loss of thymidine kinase 2 alters neuronal bioenergetics and leads to neurodegeneration. Hum Mol Genet. 19:1669-77.
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Blakely, et al. (Apr. 14, 2008) Novel mutations in the TK2 gene associated with fatal mitochondrial DNA depletion myopathy. Neuromuscular Disorders 18:557-560.
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Bourdon, et al. (May 7, 2007) Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion. Nat Genet 39: 776-780.
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Chanprasert, et al. (Jul. 10, 2013) Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene. Mol Genet Metab. 110:153-…
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Chanprasert, et al. (Dec. 6, 2012) TK2-Related Mitochondrial DNA Depletion Syndrome, Myopathic Form. GeneReviews® Internet.
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Collins, et al. (Aug. 4, 2009) Progressive myofiber loss with extensive fibro-fatty replacement in a child with mitochondrial DNA depletion syndrome and novel thymidine kinase 2 gene mutations. Neuromuscular Disorders 1…
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Copeland (Mar. 21, 2008) Inherited mitochondrial diseases of DNA replication. Ann. Rev. Med. 59:131-146.
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DiMauro, et al. (Feb. 20, 1987) Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol 22: 498-506.
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DiMauro, Schon. (Jul. 1, 2003) Mitochondrial respiratory-chain diseases. N Engl J Med 348:2656-2668.
[cited by applicant]
DiMauro, Hirano. (2005) Mitochondrial encephalomyopathies: an update. Neuromuscul Disord 15:276-286. Accepted Dec. 10, 2004.
[cited by applicant]
Dorado, et al. (2011) Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation. Hum Mol Genet. 20:155-64. Accepted Oct. 6, 2010.
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Elpeleg, et al. (Apr. 7, 2005) Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion. Am J Hum Genet 76: 1081-1086.
[cited by applicant]
Ferraro, et al. (2010) Quantitation of cellular deoxynucleoside triphosphates. Nucleic Acids Research 38: e85. Accepted Nov. 18, 2009.
[cited by applicant]
Galbiati, et al. (2006) New mutations in TK2 gene associated with mitochondrial DNA depletion. Pediatr Neurol 34: 177-185. Accepted Jul. 11, 2005.
[cited by applicant]
Garone, et al. (Sep. 10, 2012). MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA Deletions. Arch Neurol 69:1648-1651.
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Gotz, et al. (Sep. 3, 2008) Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome. Brain 131:2841-2850.
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Leshinsky-Silver, et al. (2008) A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletion. Eur J Paediatr Neurol 12:309-13. Accepted Sep. 2, 2007.
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Lesko, et al. (2010) Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion. Neuromuscul Disord 20:198-203. Accepted Nov. 25, 2009.
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Lopez, et al. (2009) Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase deficient mice. Hum Mol Genet 18: 714-722. Accepted Nov. 19, 2008.
[cited by applicant]
Mancuso, et al. (Jul. 2003) Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene. Arch Neurol. 60:1007-9.
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Mancuso, et al. (Jun. 20, 2002) Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA. Neurology. 59:1197-202.
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Mandel, et al. (Nov. 2001) The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. Nat Genet 29: 337-341.
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Martí, et al. (Apr. 8, 2010) Hearing loss in a patient with the myopathic form of mitochondrial DNA depletion syndrome and a novel mutation in the TK2 gene. Pediatr Res. 68:151-4.
[cited by applicant]
Martí, et al. (2012) Measurement of mitochondrial dNTP pools. Methods Mol Biol 837: 135-148. Dec. 20, 2011.
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Naviaux, Nguyen. (Feb. 4, 2004) POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann Neurol 55: 706-712.
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Oskoui, et al. (Aug. 2006) Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene. Arch Neurol 63:1122-1126.
[cited by applicant]
Ostergaard, et al. (Apr. 26, 2007) Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion. Am J Hum Genet 81: 383-387.
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Paradas, et al. (2012) TK2 mutation presenting as indolent myopathy. Neurology 29:504-506. Jan. 9, 2013.
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Roos, et al. (May 20, 2014) Mitochondrial DNA depletion in single fibers in a patient with novel TK2 mutations. Neuromuscul Disord. 24:713-20.
[cited by applicant]
Saada, et al. (Oct. 22, 2001) Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy. Nat Genet 29:342-344.
[cited by applicant]
Saada, et al. (Aug. 7, 2003) Mitochondrial deoxyribonucleoside triphosphate pools in thymidine kinase 2 deficiency. Biochem Biophys Res Commun 310:963-966.
[cited by applicant]
Spinazzola, et al. (Apr. 2, 2006) MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion. Nat Genet 38: 570-575.
[cited by applicant]
Tulinius, et al. (Mar. 6, 2005) Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion. Neuromuscul Disord. 15:412-415.
[cited by applicant]
Tyynismaa, et al. (2012) Thymidine kinase 2 mutations in autosomal recessive progressive exgternal ophthalmoplegia with multiple mitochondrial DNA deletions. Hum Mol Genet 21:66-75. Accepted Sep. 19, 2011.
[cited by applicant]
Vilà, et al. (Apr. 2003) Reversion of mtDNA depletion in a patient with TK2 deficiency. Neurology 60:1203-1205.
[cited by applicant]
Wang, et al. (2005) Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes. Mol Genet Metab. 84:75-82. Available online…
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Garonoe et al., “Deoxypyrimidine monophosphate bypass therapy for thymidine kinase 2 deficiency”. EMBO Mol Med Jun. 26, 2014 vol. 6 No. 8 pp. 1016-1027. Especially abstract, p. 1016 col. 2, p. 1017 col. 1 para 2, para 2…
[cited by applicant]
MedChem Express. Tipiracil hydrochloride (online) 2014 [retrieved Oct. 26, 2016] Available on the internet: <ULR: https://www.medchemexpress.com/Tipiracilhydrochloride.html?gclid=CjOKEQjwqMHABRDV16_hqKGDyNIBEiQAN-O9hEkN…
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Camara et al. “Feeding the deoxyribonucleoside salvage pathway to rescue mitochondrial DNA”. Drug Discov Today Oct. 2013 vol. 18 No. 19-20 pp. 950-957. Especially p. 955 col. 5 para 3-4.
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Garone et al., “Clinical and genetic spectrum of mitochondrial meurogastrointestinal encephalomyopathy”. Brain Nov. 2011 vol. 134 Pt 11 pp. 3326-3332. Especially p. 3328 col. 1 para 3.
[cited by applicant]
Carver, Jane D. “Dietary nucleotides: cellular immune, intestinal and hepatic system effects.” The Journal of nutrition 124.suppl_1 (1994): 144S-148S.
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Sonoda, Tomoko, and Masamiti Tatibana. “Metabolic fate of pyrimidines and purines in dietary nucleic acids ingested by mice.” Biochimica et Biophysica Acta (BBA)-Nucleic Acids and Protein Synthesis 521.1 (1978): 55-66.
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[cited by applicant]
Cámara, Yolanda, et al. “Feeding the deoxyribonucleoside salvage pathway to rescue mitochondrial DNA.” Drug discovery today 18.19-20 (Oct. 2013): 950-957.
[cited by applicant]
https://grantome.com/grant/NIH/P01-HD080642-01-5121, May 31, 2015 publication date asserted by SIPO in counterpart China Divisional Patent Application No. 2023107576092, budget start date of Sep. 30, 2014.
[cited by applicant]
Ramón et al., “Therapy Prospects for Mitochondrial DNA Maintenance Disorders,” Int. J. Mol. Sci., Jun. 16, 2021, vol. 22, No. 6447, 35 pages.
[cited by applicant]
Dombi et al., “Nucleoside Supplements as Treatments for Mitochondrial DNA Depletion Syndrome,” Front. Cell Dev. Biol., Apr. 2, 2024, vol. 12, No. 1260496, 17 pages.
[cited by applicant]
https://grantome.com/grant/NIH/P01-HD080642-01-5121, likely published in RePORTER on Monday Oct. 6, 2014 according to NIH RePORT Support Team.
[cited by applicant]