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 *

48 related articles for article (PubMed ID: 3178779)

  • 1. Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene.
    Rosenthal A; Speer A; Billwitz H; Cross GS; Forrest SM; Davies KE
    Biomed Biochim Acta; 1988; 47(2):K13-5. PubMed ID: 3178779
    [No Abstract]   [Full Text] [Related]  

  • 2. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP; Neve RL; Colletti-Feener C; Bertelson CJ; Kurnit DM; Kunkel LM
    Nature; 1986 Oct 16-22; 323(6089):646-50. PubMed ID: 3773991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Expression of the putative Duchenne muscular dystrophy gene in differentiated myogenic cell cultures and in the brain.
    Nudel U; Robzyk K; Yaffe D
    Nature; 1988 Feb; 331(6157):635-8. PubMed ID: 3340214
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patient.
    Prior TW; Papp AC; Snyder PJ; Burghes AH; Bartolo C; Sedra MS; Western LM; Mendell JR
    Nat Genet; 1993 Aug; 4(4):357-60. PubMed ID: 8401582
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Specific T cell receptor gene rearrangements at the site of muscle degeneration in Duchenne muscular dystrophy.
    Gussoni E; Pavlath GK; Miller RG; Panzara MA; Powell M; Blau HM; Steinman L
    J Immunol; 1994 Nov; 153(10):4798-805. PubMed ID: 7963545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family.
    Frydman M; Straussberg R; Shomrat R; Goebel H; Legum C; Shiloh Y
    Am J Med Genet; 1995 Sep; 58(3):209-12. PubMed ID: 8533818
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pathophysiology of muscular dystrophy.
    Partridge T
    Br J Hosp Med; 1993 Jan 6-19; 49(1):26-36. PubMed ID: 8431724
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testing.
    Prior TW; Wenger GD; Papp AC; Snyder PJ; Sedra MS; Bartolo C; Moore JW; Highsmith WE
    Hum Mutat; 1995; 5(3):263-8. PubMed ID: 7599638
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.
    Nishio H; Takeshima Y; Narita N; Yanagawa H; Suzuki Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M
    J Clin Invest; 1994 Sep; 94(3):1037-42. PubMed ID: 8083345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.
    Narita N; Nishio H; Kitoh Y; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M
    J Clin Invest; 1993 May; 91(5):1862-7. PubMed ID: 8387534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
    Heilig R; Lemaire C; Mandel JL; Dandolo L; Amar L; Avner P
    Nature; 1987 Jul 9-15; 328(6126):168-70. PubMed ID: 3600794
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N; Cross GS; Cavanna JS; Fisher EM; Lyon MF; Davies KE; Brown SD
    Nature; 1987 Jul 9-15; 328(6126):166-8. PubMed ID: 3600793
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.
    Koenig M; Hoffman EP; Bertelson CJ; Monaco AP; Feener C; Kunkel LM
    Cell; 1987 Jul; 50(3):509-17. PubMed ID: 3607877
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Rapid screening of the Duchenne muscular dystrophy gene deletion by two multiplex PCR].
    Ma S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Feb; 15(1):74-8. PubMed ID: 8324844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular studies of progressive muscular dystrophy (Duchenne).
    Kunkel LM; Monaco AP; Hoffman E; Koenig M; Feener C; Bertelson C
    Enzyme; 1987; 38(1-4):72-5. PubMed ID: 3440453
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL; Ji L; Li YD
    Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.
    Kawai H; Akaike M; Endo T; Adachi K; Inui T; Mitsui T; Kashiwagi S; Fujiwara T; Okuno S; Shin S
    J Clin Invest; 1995 Sep; 96(3):1202-7. PubMed ID: 7657792
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis.
    Patiño A; Narbona J; García-Delgado M
    Am J Med Genet; 1995 Nov; 59(2):182-7. PubMed ID: 8588583
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duchenne muscular dystrophy. Collaboration and progress.
    Goodfellow PN
    Nature; 1986 Jul 3-9; 322(6074):12-3. PubMed ID: 3724849
    [No Abstract]   [Full Text] [Related]  

  • 20. Conservation of the Duchenne muscular dystrophy gene in mice and humans.
    Hoffman EP; Monaco AP; Feener CC; Kunkel LM
    Science; 1987 Oct; 238(4825):347-50. PubMed ID: 3659917
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.