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 *

96 related articles for article (PubMed ID: 16922691)

  • 1. Huge proteins in the human proteome and their participation in hereditary diseases.
    Sakharkar MK; Kangueane P; Sakharkar KR; Zhong Z
    In Silico Biol; 2006; 6(4):275-9. PubMed ID: 16922691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proteomics approaches to study genetic and metabolic disorders.
    Gloerich J; Wevers RA; Smeitink JA; van Engelen BG; van den Heuvel LP
    J Proteome Res; 2007 Feb; 6(2):506-12. PubMed ID: 17269707
    [TBL] [Abstract][Full Text] [Related]  

  • 3. mRNA Metabolism and hereditary disorders: a tale of surveillance and escape.
    Neu-Yilik G; Kulozik AE
    Klin Padiatr; 2004; 216(6):304-14. PubMed ID: 15565545
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Variations of the length of exons and introns in human genome genes].
    Ivashchenko AT; Khaĭlenko VA; Atambaeva ShA
    Genetika; 2009 Jan; 45(1):22-9. PubMed ID: 19239093
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RNA-binding proteins in human genetic disease.
    Lukong KE; Chang KW; Khandjian EW; Richard S
    Trends Genet; 2008 Aug; 24(8):416-25. PubMed ID: 18597886
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Molecular biological studies of hereditary diseases].
    Bochkov NP; Limborskaia SA
    Vestn Akad Med Nauk SSSR; 1979; (8):35-42. PubMed ID: 494718
    [No Abstract]   [Full Text] [Related]  

  • 7. Spatial positions of homopolymeric repeats in the human proteome and their effect on cellular toxicity.
    Siwach P; Sengupta S; Parihar R; Ganesh S
    Biochem Biophys Res Commun; 2009 Mar; 380(2):382-6. PubMed ID: 19250635
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The origins of modern proteomes.
    Kurland CG; Canbäck B; Berg OG
    Biochimie; 2007 Dec; 89(12):1454-63. PubMed ID: 17949885
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel human pathological mutations.
    Hum Genet; 2008 Jun; 123(5):537-55. PubMed ID: 18465145
    [No Abstract]   [Full Text] [Related]  

  • 10. Assigning functions to genes--the main challenge of the post-genomics era.
    Janitz M
    Rev Physiol Biochem Pharmacol; 2007; 159():115-29. PubMed ID: 17846923
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic defects of intracellular-membrane transport.
    Olkkonen VM; Ikonen E
    N Engl J Med; 2000 Oct; 343(15):1095-104. PubMed ID: 11027745
    [No Abstract]   [Full Text] [Related]  

  • 12. [Genetics of cytoplasmic organoids and hereditary diseases in man].
    Neĭfakh SA
    Vestn Akad Med Nauk SSSR; 1976; (7):54-61. PubMed ID: 1027302
    [No Abstract]   [Full Text] [Related]  

  • 13. Multifunctionality dominantly determines the rate of human housekeeping and tissue specific interacting protein evolution.
    Podder S; Mukhopadhyay P; Ghosh TC
    Gene; 2009 Jun; 439(1-2):11-6. PubMed ID: 19306918
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Domain altering SNPs in the human proteome and their impact on signaling pathways.
    Liu Y; Tozeren A
    PLoS One; 2010 Sep; 5(9):e12890. PubMed ID: 20886114
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PCHM: A bioinformatic resource for high-throughput human mitochondrial proteome searching and comparison.
    Kim T; Kim E; Park SJ; Joo H
    Comput Biol Med; 2009 Aug; 39(8):689-96. PubMed ID: 19541297
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Hereditary diseases in pathologoanatomy practice].
    Bochkov NP
    Arkh Patol; 2000; 62(3):5-9. PubMed ID: 10897429
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stops along the RAS pathway in human genetic disease.
    Bentires-Alj M; Kontaridis MI; Neel BG
    Nat Med; 2006 Mar; 12(3):283-5. PubMed ID: 16520774
    [No Abstract]   [Full Text] [Related]  

  • 18. [The ratio of hereditary and environmental factors in the origination of noninfectious human diseases].
    Ivanov VI
    Tsitol Genet; 1996; 30(1):36-42. PubMed ID: 8743016
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Translation matters: protein synthesis defects in inherited disease.
    Scheper GC; van der Knaap MS; Proud CG
    Nat Rev Genet; 2007 Sep; 8(9):711-23. PubMed ID: 17680008
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A human phenome-interactome network of protein complexes implicated in genetic disorders.
    Lage K; Karlberg EO; Størling ZM; Olason PI; Pedersen AG; Rigina O; Hinsby AM; Tümer Z; Pociot F; Tommerup N; Moreau Y; Brunak S
    Nat Biotechnol; 2007 Mar; 25(3):309-16. PubMed ID: 17344885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.