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 *

88 related articles for article (PubMed ID: 8162064)

  • 21. Instability of short tandem repeats (microsatellites) in human cancers.
    Wooster R; Cleton-Jansen AM; Collins N; Mangion J; Cornelis RS; Cooper CS; Gusterson BA; Ponder BA; von Deimling A; Wiestler OD
    Nat Genet; 1994 Feb; 6(2):152-6. PubMed ID: 8162069
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Absence of myotonic dystrophy protein kinase (DMPK) mRNA as a result of a triplet repeat expansion in myotonic dystrophy.
    Carango P; Noble JE; Marks HG; Funanage VL
    Genomics; 1993 Nov; 18(2):340-8. PubMed ID: 8288237
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Introduction to molecular biology and its application to pediatrics (5): clinical cases. Genetic alterations in XY gonadal dysgenesis and in myotonic dystrophy].
    Castaño L; Bilbao JR; Urrutia I
    An Esp Pediatr; 1997 May; 46(5):513-8. PubMed ID: 9297412
    [No Abstract]   [Full Text] [Related]  

  • 24. Myotonic dystrophy reviewed: back to the future?
    Wieringa B
    Hum Mol Genet; 1994 Jan; 3(1):1-7. PubMed ID: 8162011
    [No Abstract]   [Full Text] [Related]  

  • 25. Meiotic drive in female mice: an essay.
    Ruvinsky A
    Mamm Genome; 1995 May; 6(5):315-20. PubMed ID: 7626881
    [No Abstract]   [Full Text] [Related]  

  • 26. Characteristics of myotonic dystrophy in Istria: molecular genetic approach. Part II: Analysis of genetic polymorphisms.
    Medica I; Logar N; Peterlin B
    Coll Antropol; 2000 Dec; 24(2):287-94. PubMed ID: 11216395
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Meiotic drive at the myotonic dystrophy locus.
    Gennarelli M; Dallapiccola B; Baiget M; Martorell L; Novelli G
    J Med Genet; 1994 Dec; 31(12):980. PubMed ID: 7891386
    [No Abstract]   [Full Text] [Related]  

  • 28. North Eurasian origin of the myotonic dystrophy mutation.
    Novelli G; Spedini G; Destro-Bisol G; Gennarelli M; Fattorini C; Dallapiccola B
    Hum Mutat; 1994; 4(1):79-81. PubMed ID: 7951264
    [No Abstract]   [Full Text] [Related]  

  • 29. Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.
    Inglehearn CF; Gregory CY
    Am J Hum Genet; 1997 Jun; 60(6):1562-3. PubMed ID: 9199584
    [No Abstract]   [Full Text] [Related]  

  • 30. Origin of a regressed myotonic dystrophy allele.
    Giordano M; De Angelis MS; Mutani R; Richiardi PM
    J Med Genet; 1994 Feb; 31(2):130-2. PubMed ID: 8182718
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myotonic dystrophies.
    Meola G
    Curr Opin Neurol; 2000 Oct; 13(5):519-25. PubMed ID: 11073357
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic mapping of a second myotonic dystrophy locus.
    Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
    Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Questions of expansion.
    Mandel JL
    Nat Genet; 1993 May; 4(1):8-9. PubMed ID: 8513331
    [No Abstract]   [Full Text] [Related]  

  • 34. [Molecular genetic study in congenital myotonic dystrophy].
    Martín P; Sierra J; Losada A; Rufo M; Lucas M
    Rev Neurol; 1997 Jun; 25(142):833-6. PubMed ID: 9244607
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus.
    Leeflang EP; McPeek MS; Arnheim N
    Am J Hum Genet; 1996 Oct; 59(4):896-904. PubMed ID: 8808606
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Too many trinucleotide repeats.
    Davies K
    Nature; 1992 Jul; 358(6381):facing p. 91. PubMed ID: 1614518
    [No Abstract]   [Full Text] [Related]  

  • 37. [Correlation between degrees of the CTG repeat expansion and clinical features of myotonic dystrophy].
    Eguchi I; Koike R; Onodera O; Tanaka K; Kondo H; Tsuji S
    Rinsho Shinkeigaku; 1994 Feb; 34(2):118-23. PubMed ID: 8194263
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Multiple pilomatrixomata and myotonic dystrophy: a familial association.
    Geh JL; Moss AL
    Br J Plast Surg; 1999 Mar; 52(2):143-5. PubMed ID: 10434894
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG; Jacob P; O'Hoy K; MacDonald I; Mettler G; Tsilfidis C; Korneluk RG
    Am J Med Genet; 1993 Feb; 45(3):401-7. PubMed ID: 8434633
    [TBL] [Abstract][Full Text] [Related]  

  • 40. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R; Vihola A; Bachinski LL; Huoponen K; Haapasalo H; Hackman P; Zhang S; Sirito M; Kalimo H; Meola G; Horelli-Kuitunen N; Wessman M; Krahe R; Udd B
    Neuromuscul Disord; 2004 Apr; 14(4):274-83. PubMed ID: 15019706
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.