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	181.	A linkage study of the loci for Huntington's disease and some common polymorphic markers. [electronic resource] by Brackenridge, C J Case, J Chiu, E Propert, D N Teltscher, B Wallace, D C Producer: 19790223 In: Annals of human genetics vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	MITOMAP: a human mitochondrial genome database. [electronic resource] by Kogelnik, A M Lott, M T Brown, M D Navathe, S B Wallace, D C Producer: 19960410 In: Nucleic acids research vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	Immunocytochemical characterization of the mitochondrially encoded ND1 subunit of complex I (NADH : ubiquinone oxidoreductase) in rat brain. [electronic resource] by Pettus, E H Betarbet, R Cottrell, B Wallace, D C Madyastha, V Greenamyre, J T Producer: 20000717 In: Journal of neurochemistry vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	[Mitochondrial DNA variation in Kets and Nganasans and the early peoples of Northern Eurasia]. [electronic resource] by Derbeneva, O A Starikovskaia, E B Volod'ko, N V Wallace, D C Sukernik, R I Producer: 20030212 In: Genetika vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	185.	MITOMAP: an update on the status of the human mitochondrial genome database. [electronic resource] by Kogelnik, A M Lott, M T Brown, M D Navathe, S B Wallace, D C Producer: 19970228 In: Nucleic acids research vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Mitochondrial DNA polymorphisms in Italy. II. Molecular analysis of new and rare morphs from Sardinia and Rome. [electronic resource] by Santachiara Benerecetti, A S Scozzari, R Semino, O Torroni, A Brega, A Wallace, D C Producer: 19881114 In: Annals of human genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	MITOMAP: a human mitochondrial genome database--1998 update. [electronic resource] by Kogelnik, A M Lott, M T Brown, M D Navathe, S B Wallace, D C Producer: 19980218 In: Nucleic acids research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation. [electronic resource] by Brown, M D Trounce, I A Jun, A S Allen, J C Wallace, D C Producer: 20010201 In: The Journal of biological chemistry vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia. [electronic resource] by Jun, A S Trounce, I A Brown, M D Shoffner, J M Wallace, D C Producer: 19960618 In: Molecular and cellular biology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse. [electronic resource] by Levy, S E Waymire, K G Kim, Y L MacGregor, G R Wallace, D C Producer: 19990917 In: Transgenic research vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. [electronic resource] by Bonné-Tamir, B Johnson, M J Natali, A Wallace, D C Cavalli-Sforza, L L Producer: 19860409 In: American journal of human genetics vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	192.	mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World. [electronic resource] by Starikovskaya, Y B Sukernik, R I Schurr, T G Kogelnik, A M Wallace, D C Producer: 19981223 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I. [electronic resource] by Brown, M D Yang, C C Trounce, I Torroni, A Lott, M T Wallace, D C Producer: 19920901 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	194.	mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. [electronic resource] by Chen, Y S Olckers, A Schurr, T G Kogelnik, A M Huoponen, K Wallace, D C Producer: 20000531 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy. [electronic resource] by Brown, M D Torroni, A Huoponen, K Chen, Y S Lott, M T Wallace, D C Producer: 19940815 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	196.	Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. [electronic resource] by Johnson, M J Wallace, D C Ferris, S D Rattazzi, M C Cavalli-Sforza, L L Producer: 19831021 In: Journal of molecular evolution vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	197.	Renal amino acid transport in adults with oxidative phosphorylation diseases. [electronic resource] by Shoffner, J M Voljavec, A S Dixon, J Kaufman, A Wallace, D C Mitch, W E Producer: 19950717 In: Kidney international vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	Oxidative phosphorylation diseases and cerebellar ataxia. [electronic resource] by Shoffner, J M Kaufman, A Koontz, D Krawiecki, N Smith, E Topp, M Wallace, D C Producer: 19950824 In: Clinical neuroscience (New York, N.Y.) vol. 3 Availability: No items available. Save to lists Add to cart (remove)
	199.	Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease. [electronic resource] by Corral-Debrinski, M Stepien, G Shoffner, J M Lott, M T Kanter, K Wallace, D C Producer: 19911017 In: JAMA vol. 266 Availability: No items available. Save to lists Add to cart (remove)
	200.	mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. [electronic resource] by Torroni, A Lott, M T Cabell, M F Chen, Y S Lavergne, L Wallace, D C Producer: 19941025 In: American journal of human genetics vol. 55 Availability: No items available. Save to lists Add to cart (remove)

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