202 related articles for article (PubMed ID: 11576738)
1. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.
Sermon K; Seneca S; De Rycke M; Goossens V; Van de Velde H; De Vos A; Platteau P; Lissens W; Van Steirteghem A; Liebaers I
Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S77-85. PubMed ID: 11576738
[TBL] [Abstract][Full Text] [Related]
2. A simple and rapid analysis of triplet repeat diseases by expand long PCR.
Hećimović S; Vlasić J; Barisić L; Marković D; Culić V; Pavelić K
Clin Chem Lab Med; 2001 Dec; 39(12):1259-62. PubMed ID: 11798087
[TBL] [Abstract][Full Text] [Related]
3. Fragile X and other trinucleotide repeat diseases.
Wenstrom KD
Obstet Gynecol Clin North Am; 2002 Jun; 29(2):367-88, vii. PubMed ID: 12108834
[TBL] [Abstract][Full Text] [Related]
4. Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines.
Kramer PR; Pearson CE; Sinden RR
Hum Genet; 1996 Aug; 98(2):151-7. PubMed ID: 8698331
[TBL] [Abstract][Full Text] [Related]
5. [Genetic diseases and unstable expansions of trinucleotide repeats].
Mandel JL
Rev Prat; 1997 Jan; 47(2):155-61. PubMed ID: 9157513
[TBL] [Abstract][Full Text] [Related]
6. Single-cell analysis of unstable genes.
Daniels R; Holding C; Kontogianni E; Monk M
J Assist Reprod Genet; 1996 Feb; 13(2):163-9. PubMed ID: 8688590
[TBL] [Abstract][Full Text] [Related]
7. Molecular genetic analysis of trinucleotide repeat disorders (TRDs) in Indian population and application of repeat primed PCR.
Das Bhowmik A; Rangaswamaiah S; Srinivas G; Dalal AB
Eur J Med Genet; 2015 Mar; 58(3):160-7. PubMed ID: 25534560
[TBL] [Abstract][Full Text] [Related]
8. [The role of trinucleotide repeats in human genetic diseases].
Hietanen K
Duodecim; 1996; 112(3):188-93. PubMed ID: 10590627
[No Abstract] [Full Text] [Related]
9. [Triple expansion diseases: a new mutational concept].
Schorderet DF
Rev Med Suisse Romande; 1999 Feb; 119(2):103-6. PubMed ID: 10091545
[TBL] [Abstract][Full Text] [Related]
10. Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.
Hummerich H; Baxendale S; Mott R; Kirby SF; MacDonald ME; Gusella J; Lehrach H; Bates GP
Hum Mol Genet; 1994 Jan; 3(1):73-8. PubMed ID: 8162055
[TBL] [Abstract][Full Text] [Related]
11. Disabilities caused by unstable mutations in Costa Rica.
Cuenca P; Morales F; Castro I
Rev Biol Trop; 2004 Sep; 52(3):501-5. PubMed ID: 17361543
[TBL] [Abstract][Full Text] [Related]
12. PCR approach for detection of Fragile X syndrome and Huntington disease based on modified DNA: limits and utility.
Rosales-Reynoso MA; Vilatela EA; Ojeda RM; Arce-Rivas A; Sandoval L; Troyo-Sanromán R; Barros-Núñez P
Genet Test; 2007; 11(2):153-9. PubMed ID: 17627386
[TBL] [Abstract][Full Text] [Related]
13. Trinucleotide repeats in neurogenetic disorders.
Paulson HL; Fischbeck KH
Annu Rev Neurosci; 1996; 19():79-107. PubMed ID: 8833437
[TBL] [Abstract][Full Text] [Related]
14. Simple procedure for automatic detection of unstable alleles in the myotonic dystrophy and Huntington's disease loci.
Falk M; Vojtísková M; Lukás Z; Kroupová I; Froster U
Genet Test; 2006; 10(2):85-97. PubMed ID: 16792511
[TBL] [Abstract][Full Text] [Related]
15. RNA FISH for detecting expanded repeats in human diseases.
Urbanek MO; Krzyzosiak WJ
Methods; 2016 Apr; 98():115-123. PubMed ID: 26615955
[TBL] [Abstract][Full Text] [Related]
16. Trinucleotide repeat disorders in humans: discussions of mechanisms and medical issues.
Timchenko LT; Caskey CT
FASEB J; 1996 Dec; 10(14):1589-97. PubMed ID: 9002550
[TBL] [Abstract][Full Text] [Related]
17. Genes with triplet repeats: a new class of mutations causing neurological diseases.
Plassart E; Fontaine B
Biomed Pharmacother; 1994; 48(5-6):191-7. PubMed ID: 7999979
[TBL] [Abstract][Full Text] [Related]
18. FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.
Rajan-Babu IS; Lian M; Cheah FSH; Chen M; Tan ASC; Prasath EB; Loh SF; Chong SS
Expert Rev Mol Med; 2017 Jul; 19():e10. PubMed ID: 28720156
[TBL] [Abstract][Full Text] [Related]
19. Repeat RNA expansion disorders of the nervous system: post-transcriptional mechanisms and therapeutic strategies.
Schwartz JL; Jones KL; Yeo GW
Crit Rev Biochem Mol Biol; 2021 Feb; 56(1):31-53. PubMed ID: 33172304
[TBL] [Abstract][Full Text] [Related]
20. Results on single cell PCR for Huntington's gene and WAVE product analysis for preimplantation genetic diagnosis.
Drury KC; Liu MC; Lilleberg S; Kipersztok S; Williams RS
Mol Cell Endocrinol; 2001 Oct; 183 Suppl 1():S1-4. PubMed ID: 11576724
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
