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 *

81 related articles for article (PubMed ID: 7550238)

  • 1. Identification of a one-basepair deletion in exon 6 of the dystrophin gene.
    Kavaslar GN; Telatar M; Serdaroglu P; Deymeer F; Ozdemir C; Tolun A
    Hum Mutat; 1995; 6(1):85-6. PubMed ID: 7550238
    [No Abstract]   [Full Text] [Related]  

  • 2. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
    Le Thiet Thanh ; Nguyen Thi Man ; Hori S; Sewry CA; Dubowitz V; Morris GE
    Am J Med Genet; 1995 Aug; 58(2):177-86. PubMed ID: 8533812
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation.
    Wilton SD; Johnsen RD; Pedretti JR; Laing NG
    Am J Med Genet; 1993 Jun; 46(5):563-9. PubMed ID: 8322822
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M; Paditaporn R; Noonai A; Wasant P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():172-4. PubMed ID: 8629100
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Are there ethnic differences in deletions in the dystrophin gene?
    Banerjee M; Verma IC
    Am J Med Genet; 1997 Jan; 68(2):152-7. PubMed ID: 9028449
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Cloning and sequencing of the junction fragment of dystrophin gene with exons 3 to 5 deletion].
    Zhong M; Pan SY; Lu BX; Jiang L; Li W
    Nan Fang Yi Ke Da Xue Xue Bao; 2006 Jun; 26(6):757-9. PubMed ID: 16793593
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion detection in the dystrophin gene by multiplex gap ligase chain reaction and immunochromatographic strip technology.
    Jou C; Rhoads J; Bouma S; Ching S; Hoijer J; Schroeder-Poliak P; Zaun P; Smith S; Richards S; Caskey CT
    Hum Mutat; 1995; 5(1):86-93. PubMed ID: 7728154
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan].
    Odinokova ON; Puzyrev VP; Radzhabaliev ShF; Rakhmonov RA
    Genetika; 1996 Oct; 32(10):1392-5. PubMed ID: 9091412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy.
    Taşdemir HA; Topaloğlu H; Dinçer P; Göğüş S; Kotiloğlu E; Ozdirim E; Yalaz K
    Turk J Pediatr; 1997; 39(3):317-24. PubMed ID: 9339110
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.
    Prior TW; Bartolo C; Papp AC; Snyder PJ; Sedra MS; Burghes AH; Mendell JR
    Hum Mol Genet; 1994 Jul; 3(7):1173-4. PubMed ID: 7981690
    [No Abstract]   [Full Text] [Related]  

  • 14. [Detection of extensive deletions and duplications in the dystrophin gene].
    Fajkusová L; Kuhrová V; Hájek J; Fajkus J
    Cas Lek Cesk; 1997 Mar; 136(5):148-50. PubMed ID: 9221188
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.
    Shiga N; Takeshima Y; Sakamoto H; Inoue K; Yokota Y; Yokoyama M; Matsuo M
    J Clin Invest; 1997 Nov; 100(9):2204-10. PubMed ID: 9410897
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Problems found in genetic diagnosis of DMD/BMD].
    Matsuo M
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1413-5. PubMed ID: 8752414
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Infidelity in the structure of ectopic transcripts: a novel exon in lymphocyte dystrophin transcripts.
    Roberts RG; Bentley DR; Bobrow M
    Hum Mutat; 1993; 2(4):293-9. PubMed ID: 8401537
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements.
    Disset A; Bourgeois CF; Benmalek N; Claustres M; Stevenin J; Tuffery-Giraud S
    Hum Mol Genet; 2006 Mar; 15(6):999-1013. PubMed ID: 16461336
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Cloning and sequencing of junction fragment with exon 51 deletion of Dystrophin gene].
    Pan SY; Zhang C; Liu ZL; Chen GJ; Lu XL
    Yi Chuan Xue Bao; 2002 Feb; 29(2):105-10. PubMed ID: 11901990
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardation.
    Tuffery S; Lenk U; Roberts RG; Coubes C; Demaille J; Claustres M
    Hum Mutat; 1995; 6(2):126-35. PubMed ID: 7581396
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.