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Mitochondrial Genetics:     more books (100)

Length Variations in the COII-[tRNA.sup.Lys] Intergenic Region of Mitochondrial DNA in Indonesian Populations.: An article from: Human Biology by Herlina Y. Handoko, J. Koji Lum, et all 2001-04-01 Indonesian mitochondrial DNA and its opposition to a Pleistocene era origin of proto-Polynesians in island Southeast Asia.: An article from: Human Biology by Murray P. Cox, 2005-04-01 A cautionary tale on ancient migration detection: mitochondrial DNA variation in Santa Cruz Islands, Solomon Islands.: An article from: Human Biology by J.S. Friedlaender, Fred Gentz, et all 2002-06-01 Genetic diversity in managed subpopulations of Norway spruce [Picea abies (L.) Karst.] [An article from: Forest Ecology and Management] by F. Maghuly, W. Pinsker, et all Mitochondrial DNA sequence variation in Greeks.: An article from: Human Biology by Anastasia Kouvatsi, Nikoletta Karaiskou, et all 2001-12-01 Mitochondrial DNA and prehistoric settlements: native migrations on the western edge of North America.: An article from: Human Biology by Jason A. Eshleman, Ripan S. Malhi, et all 2004-02-01 Genetic differentiation of Artemia urmiana from various ecological populations of Urmia Lake assessed by PCR amplified RFLP analysis [An article from: ... of Experimental Marine Biology and Ecology] by A. Eimanifar, S. Rezvani, et all 2006-06-13 Major Mitochondrial DNA Haplotype Heterogeneity in Highland and Lowland Amerindian Populations from Bolivia.(Statistical Data Included): An article from: Human Biology by Francesc Bert, Alfons Corella, et all 2001-02-01 Mitochondrial DNA sequence variation across linguistic and geographic boundaries in Italy.: An article from: Human Biology by Guido Barbujani, Michele Stenico, et all 1996-04-01 Genomic diversities and affinities among four endogamous groups of Punjab (India) based on autosomal and mitochondrial DNA polymorphisms.: An article from: Human Biology by Inderjeet Kaur, Sangita Roy, et all 2002-12-01 Mitochondrial diversity in linguistic isolates of the Alps: a reappraisal. (Brief Communication).: An article from: Human Biology by Cristiano Vernesi, Silvia Fuselli, et all 2002-10-01 Mitochondrial DNA analysis of gene flow among six populations of collared lizards (Crotaphytus collaris) in West Central Texas.(Statistical Data Included): ... article from: The Texas Journal of Science by James H. Campbell, J. Kelly McCoy, 2002-05-01 Mitochondrial DNA Variation in Nicobarese Islanders.(Statistical Data Included): An article from: Human Biology by B.V. Ravi Prasad, Chris E. Ricker, et all 2001-10-01 Genetic Study of the Paleolithic and Neolithic Southeast Asians.: An article from: Human Biology by Hiroki Oota, Kunihiko Kurosaki, et all 2001-04-01

lists with details

41. JN 2003; Vol.16 N°2: 286-292
    Renal disease and mitochondrial genetics. Agnès Rötig INSERM Unit 393, Necker Hospital, Paris - France. Genetic heterogeneity of mitochondrial disorders.  
    http://www.sin-italia.org/jnonline/vol16n2/286.html
    
    Extractions: Table of Contents Meeting Proceeding J NEPHROL 2003; 16: 286-292 Renal disease and mitochondrial genetics Agnès Rötig - INSERM Unit 393, Necker Hospital, Paris - France Key words: Mitochondria, Respiratory chain, Tubulopathy The mitochondrial respiratory chain The mitochondrial respiratory chain (RC) catalyzes the oxidation of fuel molecules by oxygen and the concomitant energy transduction into adenosine triphosphate (ATP) via five complexes, embedded in the inner mitochondrial membrane (1) (Fig. 1). Complex I (NADH-coenzyme Q reductase) carries reducing equivalents from NADH to coenzyme Q (CoQ, ubiquinone) and consists of more than 40 different polypeptides, seven of which are encoded by mitochondrial DNA (mtDNA). Complex II (succinate-CoQ reductase) carries reducing equivalents from FADH to CoQ and contains four polypeptides, including the FAD-dependent succinate dehydrogenase and three iron-sulfur centers. This is the only complex that does not contain any mtDNA-encoded protein. Complex III (reduced CoQ-cytochrome c reductase) carries electrons from CoQ to cytochrome c . It contains 11 subunits, one of which (cytochrome

42. Oxford University Press - Genetics
    This international, edited book summarises the advances in human mitochondrial genetics made over the past decade and a half. In  
    http://www.oup.com.au/content/General.asp?ContentID=249&MasterID=216

43. MDA / Quest 6-4 / Mitochondrial Myopathy -- An Energy Crisis In The Cells
    THE mitochondrial genetics MAZE. The inheritance patterns of the mitochondrial encephalomyopathies can be quite complicated. The  
    http://www.mitoresearch.org/Quest_6_4a.htm
    
    Extractions: THE MITOCHONDRIAL GENETICS MAZE The inheritance patterns of the mitochondrial encephalomyopathies can be quite complicated. The mutations that cause these diseases can be in the chromosomes; this is what's usually meant when people talk about a genetic or inherited disease. But mitochondrial encephalomyopathies have a unique situation. People can also inherit one of these diseases through mutations in the mitochondrial DNA (mtDNA), which comes from the mother only. Mitochondria are the only parts of the cells that have their own DNA, separate from that of the chromosomes in the cell's nucleus, called nuclear DNA. This situation occurs because the mitochondrial respiratory chain, which is the final step in the energy-making process, is made up of proteins that come from both nuclear and mtDNA (see illustration). Although only 13 of roughly 100 respiratory chain proteins come from the mtDNA, these 13 proteins contribute to every part of the respiratory chain except complex II, and 24 other mitochondrial genes are required just to manufacture those 13 proteins. Thus, a defect in either a nuclear gene or one of the 37 mitochondrial genes can cause the respiratory chain to break down. (This respiratory chain has nothing to do with breathing.) When mitochondrial disease is caused by defects in the nuclear DNA, the inheritance follows a "Mendelian" pattern, just as other inherited disorders do (named for Gregor Mendel, the 19th-century scientist who first explained inheritance). These inheritance patterns include autosomal dominant, autosomal recessive and X-linked. Leigh syndrome (caused by defects in complexes I and IV) is one of the most common forms of mitochondrial encephalomyopathy inherited in this fashion. It's usually autosomal recessive, meaning that two copies of the defective gene, one from each parent, are required to produce the disease.

44. Molecular Biology & Genetics At Cornell University, Ithaca, New York.
    plants. She also has a significant research involvement in the mitochondrial genetics of higher plants, notably Petunia. Charles  
    http://www.mbg.cornell.edu/grad/gradhistG.html
    
    Extractions: AT CORNELL UNIVERSITY Antonie Blackler The geneticists of the new Section were drawn, for the most part, from the Department of Plant Breeding. This Department had a distinguished history that could be traced back to the era of Rollins A. Emerson and his "school" of maize geneticists of the 1920s and '30s. Emerson's group carried out research that established maize as one of the best known 'genetic' organisms and worked out many extensions of Mendelian principles. Some of Emerson's students and others associated with his group went on to be the most influential geneticists of their generation the Nobel laureates George W. Beadle and Barbara McClintock, and the distinguished geneticists Milislav Demerec, Marcus Rhoades, George Sprague, Charles Burnham, and E.G. Anderson In 1964 the geneticists of the new Section were Bruce Wallace, a population geneticist who did his experimental work with Drosophila ; Harry Stinson, an Oenothera geneticist; and Adrian Srb, a fungal geneticist working primarily with Neurospora . The need for strength in the biochemical aspects of genetics was met by a new faculty appointment

45. NEJM -- Another Surprise From The Mitochondrial Genome
    Advances in the field of mitochondrial genetics have challenged the general principles of molecular biology on several occasions.  
    http://content.nejm.org/cgi/content/short/347/8/609
    
    Extractions: Add to Personal Archive ... PubMed Citation Advances in the field of mitochondrial genetics have challenged the general principles of molecular biology on several occasions. The universality of the genetic code that relates triplet-nucleotide sequences in DNA to specific amino acids in proteins was overturned by the discovery that the translation of mitochondrial proteins involves different coding rules. Studies of mitochondria led to the surprising discoveries of autocatalytic RNA (RNA with enzymatic activity in the absence of proteins), RNA editing (post-transcriptional modification of the nucleotide sequence in messenger RNA [mRNA]), and trans-splicing (the joining of two separate primary RNA transcripts to form a single mRNA molecule).

46. National Academy Of Sciences - Members
    Levings, CS North Carolina State University. Levings opened up the field and emerged as the major world figure in higher plant mitochondrial genetics.  
    http://www4.nationalacademies.org/nas/naspub.nsf/(urllinks)/NAS-58N334?opendocum

47. OUP USA: Genetics Of Mitochondrial Diseases: Ian James Holt
    book is a new addition to the successful Oxford Monographs on Medical Genetics series, providing a comprehensive review of the area of mitochondrial genetics.  
    http://www.oup.com/us/catalog/general/subject/Medicine/Genetics/?ci=0198508654&v

48. Modelling Mitochondrial Genetics
    Modelling mitochondrial genetics Mitochondria are the parts of the cell that generate energy. These cellular organelles contain  
    http://www.math.umn.edu/~yjkim/biogroup/01sep1.html

49. Advanced Human Genetics MBG 7600
    3/1/2002, F, Journal Club Multifactorial inheritance/ Linkage analysis, Tromp, 3/6/2002, W, mitochondrial genetics and human mitochondrial diseases, Grossman,  
    http://www.genetics.wayne.edu/mbg7600/mbg7600_w2002.html
    
    Extractions: Advanced Human Genetics MBG 7600 (4 credits) Winter Term - 2002 Wednesdays and Fridays at 3:00-4:50 p.m., in 2268 Scott Hall Course coordinator: John Tomkiel , Ph.D., Assistant Professor 5117 Biological Sciences Building Tel. (313) 577-1976 Fax: (313) 577-6200 e-mail: jtomkiel@geneitcs.wayne.edu date day topic Lecturer W Course Introduction Tomkiel F Human Chromosomes I Feldman W Human Chromosomes II/Karyotype analysis Heng F Chromosome Structure/Organization Tomkiel W Imprinting Tomkiel F X inactivation Tomkiel W Journal club - chromosomes/epigenetic phenomena Tomkiel F Mutational Analysis I - mutagens Kuivaniemi W Mutational Analysis II - types Kuivaniemi F Journal Club - disease gene identification Kuivaniemi W DNA Linkage Analysis Barnholtz-Sloan F DNA Linkage Analysis Barnholtz-Sloan W Exam I lectures 1/9-2/8 F Multifactorial inheritance Tromp W Multifactorial inheritance Tromp F Journal Club - Multifactorial inheritance/ Linkage analysis Tromp W Mitochondrial Genetics and human mitochondrial diseases Grossman F Developmental Genetics - animal models/stem cells/trangeni cs Li W SPRING BREAK F SPRING BREAK W Journal club- animal models for human disease Li F Exam II lectures 2/13 -3/13 W Genetic Testing and risk assessment Greb F Preimplantation diagnoses/mutation detection Hughes W Neurogenetics Kamholz F Genome Analysis Finley W Gene Therapy Kuivaniemi F Human viruses Lancaster W Cancer genetics Tainsky F Cancer Genetics Tainsky W Final exam lectures 3/17 -4/19 CMMG Home Calendar Directory Facilities ... Wayne State University For more information, please send inquiries to:

50. Press Release
    mitochondrial genetics is improving our understanding of human evolution and prehistoric migratory patterns. In addition, mitochondrial  
    http://www.mitokor.com/news/release/20020409
    
    Extractions: Careers Contact Us Search Establishes publicly available database of human mitochondrial genome sequences SAN DIEGO, CA (April 9, 2002) - MitoKor today announced the publication of a large, wide ranging study analyzing the mitochondrial DNA sequences of more than 500 individuals of different ethnic origins in The American Journal of Human Genetics. The study succeeded in identifying novel patterns arising from geographically distinct subpopulations, and will form the basis of ongoing investigations aimed at uncovering the association of variations in mitochondrial DNA with diseases of aging such as Alzheimer's and type 2 diabetes mellitus. The data may be accessed at http://www.mitokor.com/science/560mtdnas.php The paper entitled: 'Reduced-median-network analysis of complete mitochondrial DNA coding region sequences for the major African, Asian, and European haplogroups,' outlines a large DNA sequencing study undertaken at MitoKor in collaboration with scientists from the University of Newcastle upon Tyne, England, the VA Medical Center and University of California, San Diego, and Massachusetts General Hospital, Harvard Medical School. The study analyzed mitochondrial DNA sequence variations between ethnically diverse populations providing important information concerning human molecular evolution and population genetics. This data will also form the basis from which to understand how changes in mitochondrial DNA sequence can affect susceptibility to disease.

51. Mitochondrial Research Interest Group, URMC
    Ph.D. Assistant Professor in Human Genetics and Director of mitochondrial genetics Laboratory, Cincinnati Children s Hospital Medical Center Nuclear Modifier  
    http://www.urmc.rochester.edu/mrig/seminars2002.html

52. UCI Ecology And Evolutionary Biology
    Life Foundation Award for Medical Research in Alzheimer s Disease 2000 Passano Award 2000 for mitochondrial genetics, with Guiseppi Attardi 2000 Docteur  
    http://ecoevo.bio.uci.edu/Faculty/Wallace/wallace.html

53. CMGS-Mitochondrial Diseases (2)/28.11.00
    Nature Genetics 14 p146150. Lightowlers et al., (1997) Mammalian mitochondrial genetics hereditary, heteroplasmy and disease. TIG vol 13, p450-454.  
    http://www.ich.ucl.ac.uk/cmgs/mt2inh00.htm
    
    Extractions: Complex Inheritance - MRCPath course 2000-2001 Mitochondrial diseases (2) Segregation of mitochondria/ mitochondrial bottlenecks There is no strict definition for mitochondrial bottleneck. It has been described as an event, a series of events, at one or several stages of oogenesis. mtDNA molecules are selectively sampled from a large population for transmission and amplification. Recent reports indicate that recombination does not occur in mtDNA, therefore a different mechanism must account for genetic variation. A possible mechanism is a "bottleneck", ie. reduction in the number of mtDNA molecules during oogenesis. Followed by a rapid increase in mature oocytes (>100,000 copies). At some point the number of mtDNA molecules must decrease again to approx. 200 copies per cells in the oogonium. 1982- Study using Holstein cows.

54. European Science Foundation Workshop On "Trends In Mitochondrial Pharmacology An
    attention will be put to mitochondria as a target for various therapeutically applied substances and achievements in mitochondrial genetics and mitochondrially  
    http://www.nencki.gov.pl/iiclab/esf.html
    
    Extractions: on the site: Last modified: Webmaster: Wojciech Wojtowicz wwojtowi@ibb.waw.pl European Science Foundation workshop on Trends in Mitochondrial Pharmacology and Genetics 9-12 May 2003, Warsaw-M±dralin, POLAND Organizer: Nencki Institute of Experimental Biology Invitation The purpose of the Workshop will be to sum up recent state of our knowledge on mitochondrial functions within the cell with the numerous aspects of cell energetics, development and transformation. Special attention will be put to mitochondria as a target for various therapeutically applied substances and achievements in mitochondrial genetics and mitochondrially based diseases. This exchange of information, ideas and experience will form a basis for European scientific collaboration.

55. Obsah JAB
    The chromosome end replication lessons from mitochondrial genetics Jozef Nosek, Lubomir Tomaska and Blanka Kucejova Address Jozef Nosek, Department of  
    http://www.zsf.jcu.cz/vyzkum/jab/2_2/nosek.htm

56. Mitochondrial Biogenesis And Genetics, Part B
    Features This volume covers methodology used in Mitochondrial gene expression mitochondrial genetics and gene manipulation Mitochondrial diseases and aging.  
    http://www.harcourt-international.com/catalogue/title.cfm?ISBN=012182165X

57. Highlight_archive2000_mf.html
    84 . mitochondrial genetics A clever way to model defects . . . 84 . mitochondrial genetics . . . and a new way to rescue them. 85 .  
    http://www.nature.com/nrg/archive/highlight_archive2000_mf.html

58. SCU | Centre For Animal Conservation Genetics
    Susan Fuller Molecular phylogenetics of the world s goannas. Fiona Harriss - PhD mitochondrial genetics of island populations of the Australian bush rat.  
    http://www.scu.edu.au/research/cacg/ppstudies.html
    
    Extractions: Nick Campbell - PhD: Mitochondrial Control Region variation in two genera of Australian rodents; Melomys and Uromys. Application to phylogenetics, phylogeography and conservation. Jenny Seddon - MSc: Molecular phylogeny of the Gondwanan turtles Tania Dow - BSc Hons: Maternal population genetic structure of the endangered Hastings River mouse Steve Garland - BSc Hons: Myoglobin intron variation in Australian Rattus Dean Jerry - PhD: Population ecology and genetics of the Australian bass, Macquaria novemaculeata. Toni Pacey - BSc Hons: Molecular evolutionary relationships of the marsupials: superfamily Peramelomorphia. Carol Todd - MSc: Population genetics of buffalo fly in Australia. Susan Fuller - Molecular phylogenetics of the world's goannas. Fiona Harriss - PhD: Mitochondrial genetics of island populations of the Australian bush rat. Jenny Seddon - PhD: Mhc variation in island populations of the Australian bush rat.

59. MU IPG Faculty: Kathleen J. Newton
    Biological Sciences 105 Tucker Hall University of MissouriColumbia Columbia, MO 65211. Website Plant molecular genetics and mitochondrial genetics.  
    http://www.plantgroup.org/faculty-view.php?id=26

60. OUP: Genetics Of Mitochondrial Diseases: Holt
    Genetics of Mitochondrial diseases. This international edited book summarises the advances in human mitochondrial genetics made over the past decade and a half.  
    http://www.oup.co.uk/isbn/0-19-850865-4
    
    Extractions: VIEW BASKET Quick Links About OUP Career Opportunities Contacts Need help? oup.com Search the Catalogue Site Index American National Biography Booksellers' Information Service Children's Fiction and Poetry Children's Reference Dictionaries Dictionary of National Biography Digital Reference English Language Teaching Higher Education Textbooks Humanities International Education Unit Journals Law Medicine Music Oxford English Dictionary Reference Rights and Permissions Science School Books Social Sciences World's Classics UK and Europe Book Catalogue Help with online ordering How to order Postage Returns policy ... Table of contents Edited by Ian James Holt

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