These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 18518963)

  • 1. Mutation patterns of mtDNA: empirical inferences for the coding region.
    Santos C; Montiel R; Arruda A; Alvarez L; Aluja MP; Lima M
    BMC Evol Biol; 2008 Jun; 8():167. PubMed ID: 18518963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Understanding differences between phylogenetic and pedigree-derived mtDNA mutation rate: a model using families from the Azores Islands (Portugal).
    Santos C; Montiel R; Sierra B; Bettencourt C; Fernandez E; Alvarez L; Lima M; Abade A; Aluja MP
    Mol Biol Evol; 2005 Jun; 22(6):1490-505. PubMed ID: 15814829
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of mitochondrial DNA variations in Indian patients with congenital cataract.
    Roshan M; Kabekkodu SP; Vijaya PH; Manjunath K; Graw J; Gopinath PM; Satyamoorthy K
    Mol Vis; 2012; 18():181-93. PubMed ID: 22312186
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Koolkarnkhai P; Intakham C; Sangthong P; Surat W; Wonnapinij P
    Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Dec; 30(8):848-860. PubMed ID: 31766903
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complete mtDNA genomes reveal similar penetrances of maternally inherited type 2 diabetes in two Chinese families.
    Yang Y; Zhou T; Peng M; Liu Y; Li Y; Wang H; Irwin DM; Zhang Y
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 May; 27(3):2040-4. PubMed ID: 25469813
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel G3337A mitochondrial ND1 mutation related to cardiomyopathy co-segregates with tRNALeu(CUN) A12308G and tRNAThr C15946T mutations.
    Zifa E; Theotokis P; Kaminari A; Maridaki H; Leze H; Petsiava E; Mamuris Z; Stathopoulos C
    Mitochondrion; 2008 Jun; 8(3):229-36. PubMed ID: 18502698
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region.
    Finnilä S; Hassinen IE; Majamaa K
    Mutat Res; 2001 Jun; 458(1-2):31-9. PubMed ID: 11406419
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.
    Finnilä S; Hassinen IE; Ala-Kokko L; Majamaa K
    Am J Hum Genet; 2000 Mar; 66(3):1017-26. PubMed ID: 10712215
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phylogenetic network for European mtDNA.
    Finnilä S; Lehtonen MS; Majamaa K
    Am J Hum Genet; 2001 Jun; 68(6):1475-84. PubMed ID: 11349229
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MtDNA substitution rate and segregation of heteroplasmy in coding and noncoding regions.
    Cavelier L; Jazin E; Jalonen P; Gyllensten U
    Hum Genet; 2000 Jul; 107(1):45-50. PubMed ID: 10982034
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy.
    Mahjoub S; Sternberg D; Boussaada R; Filaut S; Gmira F; Mechmech R; Jardel C; Arab SB
    Diagn Mol Pathol; 2007 Dec; 16(4):238-42. PubMed ID: 18043288
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.
    Hotta O; Inoue CN; Miyabayashi S; Furuta T; Takeuchi A; Taguma Y
    Kidney Int; 2001 Apr; 59(4):1236-43. PubMed ID: 11260383
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations.
    Ballana E; Govea N; de Cid R; Garcia C; Arribas C; Rosell J; Estivill X
    Hum Mutat; 2008 Feb; 29(2):248-57. PubMed ID: 17999439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
    Annunen-Rasila J; Finnilä S; Mykkänen K; Moilanen JS; Veijola J; Pöyhönen M; Viitanen M; Kalimo H; Majamaa K
    Neurogenetics; 2006 Jul; 7(3):185-94. PubMed ID: 16807713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.
    Kang E; Wu J; Gutierrez NM; Koski A; Tippner-Hedges R; Agaronyan K; Platero-Luengo A; Martinez-Redondo P; Ma H; Lee Y; Hayama T; Van Dyken C; Wang X; Luo S; Ahmed R; Li Y; Ji D; Kayali R; Cinnioglu C; Olson S; Jensen J; Battaglia D; Lee D; Wu D; Huang T; Wolf DP; Temiakov D; Belmonte JC; Amato P; Mitalipov S
    Nature; 2016 Dec; 540(7632):270-275. PubMed ID: 27919073
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA intra-individual variation in a bumblebee species: A challenge for evolutionary studies and molecular identification.
    Ricardo PC; Françoso E; Arias MC
    Mitochondrion; 2020 Jul; 53():243-254. PubMed ID: 32569843
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic structure and origin of peopling in the Azores islands (Portugal): the view from mtDNA.
    Santos C; Lima M; Montiel R; Angles N; Pires L; Abade A; Aluja MP
    Ann Hum Genet; 2003 Sep; 67(Pt 5):433-56. PubMed ID: 12940917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pedigree analysis and sequence analysis of mtDNA 12srRNA, tRNA(Leu(UUR)), tRNA(Ser(UCN)) gene in nonsyndromic inherited deafness pedigrees].
    Li W; Han D; Yuan H; Cao J
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2004 Oct; 18(10):582-5, 589. PubMed ID: 15620132
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J.
    Moilanen JS; Finnila S; Majamaa K
    Mol Biol Evol; 2003 Dec; 20(12):2132-42. PubMed ID: 12949126
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MtDNA mutations in maternally inherited diabetes: presence of the 3397 ND1 mutation previously associated with Alzheimer's and Parkinson's disease.
    Cavelier L; Erikson I; Tammi M; Jalonen P; Lindholm E; Jazin E; Smith P; Luthman H; Gyllensten U
    Hereditas; 2001; 135(1):65-70. PubMed ID: 12035616
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.