212 related articles for article (PubMed ID: 21180173)
1. [Study of the gene deletions and the immunofluorescence of muscle in patients with DMD/BMD].
Dong YH; Lu PY; Wei C; Wang HB; Zhao BH
Zhongguo Ying Yong Sheng Li Xue Za Zhi; 2005 Nov; 21(4):453-6. PubMed ID: 21180173
[TBL] [Abstract][Full Text] [Related]
2. [Combining approach with multiplex PCR and MLPA to detect deletion and duplication in DMD patients, carriers, and prenatal diagnosis].
Li H; Ding J; Wang W; Chen Y; Lu W; Shao H; Wu BL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):318-22. PubMed ID: 19504448
[TBL] [Abstract][Full Text] [Related]
3. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
Al-Jumah M; Majumdar R; Al-Rajeh S; Chaves-Carballo E; Salih MM; Awada A; Al-Shahwan S; Al-Uthaim S
Saudi Med J; 2002 Dec; 23(12):1478-82. PubMed ID: 12518196
[TBL] [Abstract][Full Text] [Related]
4. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
Kumari D; Mital A; Gupta M; Goyle S
Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
[TBL] [Abstract][Full Text] [Related]
5. Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.
Voit T; Stuettgen P; Cremer M; Goebel HH
Neuropediatrics; 1991 Aug; 22(3):152-62. PubMed ID: 1944822
[TBL] [Abstract][Full Text] [Related]
6. Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.
Dastur RS; Kachwala MY; Khadilkar SV; Hegde MR; Gaitonde PS
Neurol India; 2011; 59(6):803-9. PubMed ID: 22234189
[TBL] [Abstract][Full Text] [Related]
7. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
Murugan S; Chandramohan A; Lakshmi BR
Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
[TBL] [Abstract][Full Text] [Related]
8. Molecular deletion patterns in Duchenne and Becker muscular dystrophy patients from KwaZulu Natal.
Hallwirth Pillay KD; Bill PL; Madurai S; Mubaiwa L; Rapiti P
J Neurol Sci; 2007 Jan; 252(1):1-3. PubMed ID: 17141273
[TBL] [Abstract][Full Text] [Related]
9. Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD/BMD patients.
Madania A; Zarzour H; Jarjour RA; Ghoury I
Clin Biochem; 2010 Jul; 43(10-11):836-42. PubMed ID: 20381484
[TBL] [Abstract][Full Text] [Related]
10. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy.
Béroud C; Tuffery-Giraud S; Matsuo M; Hamroun D; Humbertclaude V; Monnier N; Moizard MP; Voelckel MA; Calemard LM; Boisseau P; Blayau M; Philippe C; Cossée M; Pagès M; Rivier F; Danos O; Garcia L; Claustres M
Hum Mutat; 2007 Feb; 28(2):196-202. PubMed ID: 17041910
[TBL] [Abstract][Full Text] [Related]
11. [Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy].
Wang X; Xie Y; Zhang C; Liu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):239-42. PubMed ID: 12048687
[TBL] [Abstract][Full Text] [Related]
12. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
[TBL] [Abstract][Full Text] [Related]
13. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
Sertić J; Barisić N; Sostarko M; Brzović Z; Stavljenić-Rukavina A
Coll Antropol; 1997 Jun; 21(1):151-6. PubMed ID: 9225508
[TBL] [Abstract][Full Text] [Related]
14. MLPA Analyses Reveal a Spectrum of Dystrophin Gene Deletions/Duplications in Pakistani Patients Suspected of Having Duchenne/Becker Muscular Dystrophy: A Retrospective Study.
Ansar Z; Nasir A; Moatter T; Khan S; Kirmani S; Ibrahim S; Imam K; Ather A; Samreen A; Hasan Z
Genet Test Mol Biomarkers; 2019 Jul; 23(7):468-472. PubMed ID: 31157985
[No Abstract] [Full Text] [Related]
15. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
Malmgren H; White I; Johansson S; Levkov L; Iwarsson E; Fridström M; Blennow E
Mol Hum Reprod; 2006 May; 12(5):353-6. PubMed ID: 16608904
[TBL] [Abstract][Full Text] [Related]
16. The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicine.
Iskandar K; Dwianingsih EK; Pratiwi L; Kalim AS; Mardhiah H; Putranti AH; Nurputra DK; Triono A; Herini ES; Malueka RG; Gunadi ; Lai PS; Sunartini
BMC Res Notes; 2019 Oct; 12(1):704. PubMed ID: 31661024
[TBL] [Abstract][Full Text] [Related]
17. Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation.
Gentil C; Leturcq F; Ben Yaou R; Kaplan JC; Laforet P; Pénisson-Besnier I; Espil-Taris C; Voit T; Garcia L; Piétri-Rouxel F
Hum Mol Genet; 2012 Aug; 21(15):3449-60. PubMed ID: 22589245
[TBL] [Abstract][Full Text] [Related]
18. Exon deletion patterns of the dystrophin gene in 82 Vietnamese Duchenne/Becker muscular dystrophy patients.
Tran VK; Ta VT; Vu DC; Nguyen ST; Do HN; Ta MH; Tran TH; Matsuo M
J Neurogenet; 2013 Dec; 27(4):170-5. PubMed ID: 24099565
[TBL] [Abstract][Full Text] [Related]
19. Dystrophin gene analysis in Hungarian Duchenne/Becker muscular dystrophy families - detection of carrier status in symptomatic and asymptomatic female relatives.
Pikó H; Vancsó V; Nagy B; Bán Z; Herczegfalvi A; Karcagi V
Neuromuscul Disord; 2009 Feb; 19(2):108-12. PubMed ID: 19084397
[TBL] [Abstract][Full Text] [Related]
20. Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion.
Lee KA; Han SH; Choi JR; Chung JS; Choi YC
Pediatr Neurol; 2008 Aug; 39(2):129-32. PubMed ID: 18639760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
