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 *

32 related articles for article (PubMed ID: 17807305)

  • 1. ATAVIC MUTATION.
    Murdoch J
    Science; 1903 Feb; 17(423):234-5. PubMed ID: 17807305
    [No Abstract]   [Full Text] [Related]  

  • 2. [Atavic variation or abnormality].
    Navarro JA
    Estomatol Cult; 1973; 7(2):191-2. PubMed ID: 4535993
    [No Abstract]   [Full Text] [Related]  

  • 3. [An unusual case of bilateral "atavic" foot].
    Tognolo P
    Minerva Ortop; 1969 Nov; 20(11):575-8. PubMed ID: 5379278
    [No Abstract]   [Full Text] [Related]  

  • 4. The pterygo-spinous muscle--an aberrant (atavic) remnant.
    Nathan H
    Anat Anz; 1989; 169(2):97-9. PubMed ID: 2589640
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The 16S ribosomal RNA mutation database (16SMDB).
    Triman KL
    Nucleic Acids Res; 1994 Sep; 22(17):3563-5. PubMed ID: 7937058
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mtDNA C11777A mutation in Leigh syndrome.
    Komaki H; Akanuma J; Iwata H; Takahashi T; Mashima Y; Nonaka I; Goto Y
    Mitochondrion; 2003 Mar; 2(4):293-304. PubMed ID: 16120329
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Intermediate mutation frequencies favor evolution of multidrug resistance in Escherichia coli.
    Denamur E; Tenaillon O; Deschamps C; Skurnik D; Ronco E; Gaillard JL; Picard B; Branger C; Matic I
    Genetics; 2005 Oct; 171(2):825-7. PubMed ID: 15965238
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel elastin gene mutation (1281delC) in a family with supravalvular aortic stenosis: a mutation cluster within exon 20.
    Dedic J; Weiss AS; Katahira J; Yu B; Trent RJ; Urbán Z
    Hum Mutat; 2001; 17(1):81. PubMed ID: 11139266
    [No Abstract]   [Full Text] [Related]  

  • 9. Truly hypervariable DNA fingerprints due to exceptionally high mutation rates.
    Lubjuhn T; Sramkova A; Masello JF; Quillfeldt P; Epplen JT
    Electrophoresis; 2002 Feb; 23(4):517-9. PubMed ID: 11870758
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The effect of mutation him1 characterized by enhanced induced mutagenesis on the genetic effects of 6-N-hydroxylaminopurine in Saccharomyces cerevisiae].
    Ivanov EL; Sadykov SN; Koroleva IK
    Genetika; 1990 Jan; 26(1):30-6. PubMed ID: 2188875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Spontaneous mutation of the H-2b-haplotype in C57BL/10SnY mice].
    Blandova ZK; Rat'kin AE
    Genetika; 1987 Jul; 23(7):1334-6. PubMed ID: 3308634
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A statistical treatment of biases affecting the estimation of mutation rates.
    Vicard P; Dawid AP
    Mutat Res; 2004 Mar; 547(1-2):19-33. PubMed ID: 15013695
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spontaneous mutation rates in continuous cultures: the effect of some environmental factors.
    Savva D
    Microbios; 1982; 33(132):81-92. PubMed ID: 7050639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neighboring-site effects of amino acid mutation.
    Wang GZ; Chen LL; Zhang HY
    Biochem Biophys Res Commun; 2007 Feb; 353(3):531-4. PubMed ID: 17198679
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Study on mutation of exon 8 of Wilson's disease gene].
    Xu P; Liang X; Ma S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Apr; 16(2):88-90. PubMed ID: 10200361
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gaucher mutation N188S is associated with myoclonic epilepsy.
    Kowarz L; Goker-Alpan O; Banerjee-Basu S; LaMarca ME; Kinlaw L; Schiffmann R; Baxevanis AD; Sidransky E
    Hum Mutat; 2005 Sep; 26(3):271-3; author reply 274-5. PubMed ID: 16086325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mutation BRCA1 gene in 186 breast cancer patients].
    Lai C; Jiang Z; Song S
    Zhonghua Zhong Liu Za Zhi; 2001 Nov; 23(6):483-5. PubMed ID: 11859716
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Basilar artery thrombosis in a child heterozygous for prothrombin gene G20210A mutation.
    Hüdaoglu O; Kurul S; Yis U; Dirik E; Cakmakçi H; Men S
    J Child Neurol; 2007 Mar; 22(3):329-31. PubMed ID: 17621506
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methylation and gene mutation in eukaryotic DNA.
    Liu CQ; Huang JF; Wang Y; Liu WB
    Acta Biol Hung; 1998; 49(2-4):185-91. PubMed ID: 10526960
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation of the prothrombin gene and thrombotic events in patients with polycythemia vera or essential thrombocythemia: a cohort study.
    Gisslinger H; Müllner M; Pabinger I; Heis-Vahidi-Fard N; Gisslinger B; Brichta A; Bachleitner-Hofmann T; Mannhalter C
    Haematologica; 2005 Mar; 90(3):408-10. PubMed ID: 15749677
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 2.