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1
المؤلفون: M. T. Lott, Xiaowu Gai, Jeremy Leipzig, Marni J. Falk, Daniel Navarro-Gomez, Alphons P. M. Stassen, Janey L. Wiggs, Mannis van Oven, Lishuang Shen, Douglas C. Wallace
المساهمون: Genetic Identification
المصدر: Bioinformatics, 31(8), 1310-1312. Oxford University Press
مصطلحات موضوعية: Statistics and Probability, Mitochondrial DNA, Sequencing data, Computational biology, Biology, DNA, Mitochondrial, Biochemistry, Haplogroup, PHY, Humans, Molecular Biology, Genetics, Haplotype, Genetic Variation, High-Throughput Nucleotide Sequencing, Sequence Analysis, DNA, Applications Notes, Computer Science Applications, Computational Mathematics, Haplotypes, Computational Theory and Mathematics, Classifier (UML), Algorithms, Software, Reference genome, Human mitochondrial DNA haplogroup
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d449ace95961cfdac85e408fb1013ef
https://pure.eur.nl/en/publications/9f7ddbab-c084-4914-8bcb-fdf6ee21955d -
2
المؤلفون: M. G. Bialer, S. G. Pavlakis, Douglas C. Wallace, J. Dixon, Allan Kaufman, M. T. Lott, John M. Shoffner, S. Teichberg
المصدر: Neurology. 45:286-292
مصطلحات موضوعية: Genetics, Mitochondrial encephalomyopathy, Mutation, Mitochondrial DNA, Lineage (genetic), Mitochondrion, Biology, medicine.disease_cause, medicine.disease, Human mitochondrial genetics, Mitochondrial myopathy, medicine, Neurology (clinical), Chronic progressive external ophthalmoplegia
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::93026f958bdc87ad865988314c1fae77
https://doi.org/10.1212/wnl.45.2.286 -
3
المؤلفون: Marisol Corral-Debrinski, Terzah M. Horton, Douglas C. Wallace, M. T. Lott, M F Beal, Ann C. McKee, Brett H. Graham, John M. Shoffner
المصدر: Genomics. 23:471-476
مصطلحات موضوعية: Male, Mitochondrial DNA, medicine.medical_specialty, Cerebellum, Biology, medicine.disease_cause, DNA, Mitochondrial, Oxidative Phosphorylation, Central nervous system disease, Degenerative disease, Alzheimer Disease, Internal medicine, Genetics, medicine, Humans, Tissue Distribution, Aged, Sequence Deletion, Aged, 80 and over, Cerebral Cortex, Mutation, Putamen, Age Factors, Middle Aged, medicine.disease, Pathophysiology, Endocrinology, medicine.anatomical_structure, Female, Alzheimer's disease, DNA Damage
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4
المؤلفون: A, Torroni, M D, Brown, M T, Lott, N J, Newman, D C, Wallace
المصدر: Human mutation. 5(4)
مصطلحات موضوعية: Europe, Genetic Markers, Polymorphism, Genetic, Haplotypes, Africa, Optic Nerve Diseases, Indians, North American, Cuba, Humans, DNA, Mitochondrial, Polymerase Chain Reaction, Disease Outbreaks
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5
المؤلفون: A, Torroni, M T, Lott, M F, Cabell, Y S, Chen, L, Lavergne, D C, Wallace
المصدر: American journal of human genetics. 55(4)
مصطلحات موضوعية: Chromosome Aberrations, Canada, Base Sequence, Models, Genetic, Molecular Sequence Data, Restriction Mapping, Black People, Genetic Variation, Hominidae, Biological Evolution, DNA, Mitochondrial, Polymerase Chain Reaction, eye diseases, United States, White People, Time, Archaeology, Asian People, Haplotypes, Animals, Humans, Phylogeny, DNA Primers, Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::96396293dbd03c29167cb5424f4cc6eb
https://pubmed.ncbi.nlm.nih.gov/7942855 -
6
المؤلفون: N J, Newman, A, Torroni, M D, Brown, M T, Lott, M M, Fernandez, D C, Wallace
المصدر: American journal of ophthalmology. 118(2)
مصطلحات موضوعية: Adult, Aged, 80 and over, Electrophoresis, Agar Gel, Male, Adolescent, Cuba, Middle Aged, DNA, Mitochondrial, Polymerase Chain Reaction, Disease Outbreaks, Pedigree, Optic Atrophies, Hereditary, Mutation, Optic Nerve Diseases, Humans, Female, Child, Aged
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::2968f691d4e8633b622a36da482829e0
https://pubmed.ncbi.nlm.nih.gov/8053461 -
7
المؤلفون: A, Torroni, Y S, Chen, O, Semino, A S, Santachiara-Beneceretti, C R, Scott, M T, Lott, M, Winter, D C, Wallace
المصدر: American journal of human genetics. 54(2)
مصطلحات موضوعية: Male, Polymorphism, Genetic, Letter, Gene Frequency, Haplotypes, Y Chromosome, Humans, Female, DNA, Mitochondrial, Indians, Central American, Mexico, Phylogeny
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::409453598ae9146f02bafdb709393bfe
https://pubmed.ncbi.nlm.nih.gov/7726181 -
8
المؤلفون: Michael D. Brown, Rem I. Sukernik, Olga Derbeneva, M. T. Lott, N. V. Volodko, IY Bychkov, Irina E. Mikhailovskaya, Douglas C. Wallace, Elena B. Starikovskaya
المصدر: Journal of the Peripheral Nervous System. 7:211-212
مصطلحات موضوعية: Genetics, Mutation, Mitochondrial DNA, Natural selection, General Neuroscience, Mitochondrial disease, Point mutation, Biology, medicine.disease_cause, medicine.disease, Human mitochondrial genetics, Heteroplasmy, mitochondrial fusion, medicine, Neurology (clinical)
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المؤلفون: M D, Brown, C C, Yang, I, Trounce, A, Torroni, M T, Lott, D C, Wallace
المصدر: American journal of human genetics. 51(2)
مصطلحات موضوعية: Electron Transport Complex IV, Terminator Regions, Genetic, Base Sequence, Optic Atrophies, Hereditary, Molecular Sequence Data, Mutation, Humans, Electrophoresis, Polyacrylamide Gel, Amino Acid Sequence, DNA, Mitochondrial, eye diseases, Phylogeny, Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::de2491a3fe34c900c2134b20b7131b50
https://pubmed.ncbi.nlm.nih.gov/1322638 -
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المؤلفون: E M, Stone, N J, Newman, N R, Miller, D R, Johns, M T, Lott, D C, Wallace
المصدر: Journal of clinical neuro-ophthalmology. 12(1)
مصطلحات موضوعية: Male, Adolescent, Optic Atrophies, Hereditary, Mutation, Remission, Spontaneous, Vision Disorders, Visual Acuity, Humans, Female, Middle Aged, Visual Fields, Child, DNA, Mitochondrial
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::ab5d5fd474c6f525c5b8502d555a442a
https://pubmed.ncbi.nlm.nih.gov/1532593