63 related articles for article (PubMed ID: 34024776)
1. Massive contractions of myotonic dystrophy type 2-associated CCTG tetranucleotide repeats occur via double-strand break repair with distinct requirements for DNA helicases.
Papp D; Hernandez LA; Mai TA; Haanen TJ; O'Donnell MA; Duran AT; Hernandez SM; Narvanto JE; Arguello B; Onwukwe MO; Mirkin SM; Kim JC
G3 (Bethesda); 2024 Feb; 14(2):. PubMed ID: 37950892
[TBL] [Abstract][Full Text] [Related]
2. Myotonic Dystrophies: A Genetic Overview.
Soltanzadeh P
Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205411
[TBL] [Abstract][Full Text] [Related]
3. Myotonic dystrophy: emerging mechanisms for DM1 and DM2.
Cho DH; Tapscott SJ
Biochim Biophys Acta; 2007 Feb; 1772(2):195-204. PubMed ID: 16876389
[TBL] [Abstract][Full Text] [Related]
4. Ancestral Origin of the First Indian Families with Myotonic Dystrophy Type 2.
Damen M; Schijvenaars M; Schimmel-Naber M; Groothuismink J; Coenen M; Tieleman A
J Neuromuscul Dis; 2021; 8(4):715-722. PubMed ID: 34024776
[TBL] [Abstract][Full Text] [Related]
5. Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype.
Coenen MJ; Tieleman AA; Schijvenaars MM; Leferink M; Ranum LP; Scheffer H; van Engelen BG
Eur J Hum Genet; 2011 May; 19(5):567-70. PubMed ID: 21224892
[TBL] [Abstract][Full Text] [Related]
6. Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.
Bachinski LL; Udd B; Meola G; Sansone V; Bassez G; Eymard B; Thornton CA; Moxley RT; Harper PS; Rogers MT; Jurkat-Rott K; Lehmann-Horn F; Wieser T; Gamez J; Navarro C; Bottani A; Kohler A; Shriver MD; Sallinen R; Wessman M; Zhang S; Wright FA; Krahe R
Am J Hum Genet; 2003 Oct; 73(4):835-48. PubMed ID: 12970845
[TBL] [Abstract][Full Text] [Related]
7. Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract.
Liquori CL; Ikeda Y; Weatherspoon M; Ricker K; Schoser BG; Dalton JC; Day JW; Ranum LP
Am J Hum Genet; 2003 Oct; 73(4):849-62. PubMed ID: 14505273
[TBL] [Abstract][Full Text] [Related]
8. Myotonic dystrophy type 2 in Japan: ancestral origin distinct from Caucasian families.
Saito T; Amakusa Y; Kimura T; Yahara O; Aizawa H; Ikeda Y; Day JW; Ranum LP; Ohno K; Matsuura T
Neurogenetics; 2008 Feb; 9(1):61-3. PubMed ID: 18057971
[TBL] [Abstract][Full Text] [Related]
9. Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients.
Santoro M; Fontana L; Maiorca F; Centofanti F; Massa R; Silvestri G; Novelli G; Botta A
Biochim Biophys Acta Mol Basis Dis; 2018 Mar; 1864(3):917-924. PubMed ID: 29291944
[TBL] [Abstract][Full Text] [Related]
10. Hearing impairment in patients with myotonic dystrophy type 2.
van Vliet J; Tieleman AA; van Engelen BGM; Bassez G; Servais L; Béhin A; Stojkovic T; Meulstee J; Engel JAM; Lamas G; Eymard B; Verhagen WIM; Mamelle E
Neurology; 2018 Feb; 90(7):e615-e622. PubMed ID: 29343467
[TBL] [Abstract][Full Text] [Related]
11. Early onset posterior subscapular cataract in a series of myotonic dystrophy type 2 patients.
Papadopoulos C; Kekou K; Xirou S; Kitsiou-Tzeli S; Kararizou E; Papadimas GK
Eye (Lond); 2018 Mar; 32(3):622-625. PubMed ID: 29219952
[TBL] [Abstract][Full Text] [Related]
12. High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2.
Hilbert JE; Barohn RJ; Clemens PR; Luebbe EA; Martens WB; McDermott MP; Parkhill AL; Tawil R; Thornton CA; Moxley RT;
Neurology; 2017 Sep; 89(13):1348-1354. PubMed ID: 28855409
[TBL] [Abstract][Full Text] [Related]
13. Frontostriatal dysexecutive syndrome: a core cognitive feature of myotonic dystrophy type 2.
Peric S; Mandic-Stojmenovic G; Stefanova E; Savic-Pavicevic D; Pesovic J; Ilic V; Dobricic V; Basta I; Lavrnic D; Rakocevic-Stojanovic V
J Neurol; 2015 Jan; 262(1):142-8. PubMed ID: 25346064
[TBL] [Abstract][Full Text] [Related]
14. Diagnostic odyssey of patients with myotonic dystrophy.
Hilbert JE; Ashizawa T; Day JW; Luebbe EA; Martens WB; McDermott MP; Tawil R; Thornton CA; Moxley RT
J Neurol; 2013 Oct; 260(10):2497-504. PubMed ID: 23807151
[TBL] [Abstract][Full Text] [Related]
15. Uninterrupted CCTG tracts in the myotonic dystrophy type 2 associated locus.
Radvanszky J; Surovy M; Polak E; Kadasi L
Neuromuscul Disord; 2013 Jul; 23(7):591-8. PubMed ID: 23561036
[TBL] [Abstract][Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
