Day JW - Search Results

1

Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8.

Moseley ML, Zu T, Ikeda Y, Gao W, Mosemiller AK, Daughters RS, Chen G, Weatherspoon MR, Clark HB, Ebner TJ, Day JW, Ranum LP. Moseley ML, et al. Among authors: day jw. Nat Genet. 2006 Jul;38(7):758-69. doi: 10.1038/ng1827. Epub 2006 Jun 25. Nat Genet. 2006. PMID: 16804541

2

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.

Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LP. Koob MD, et al. Among authors: day jw. Nat Genet. 1998 Jan;18(1):72-5. doi: 10.1038/ng0198-72. Nat Genet. 1998. PMID: 9425905

3

Genetic mapping of a second myotonic dystrophy locus.

Ranum LP, Rasmussen PF, Benzow KA, Koob MD, Day JW. Ranum LP, et al. Among authors: day jw. Nat Genet. 1998 Jun;19(2):196-8. doi: 10.1038/570. Nat Genet. 1998. PMID: 9620781

4

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2).

Day JW, Roelofs R, Leroy B, Pech I, Benzow K, Ranum LP. Day JW, et al. Neuromuscul Disord. 1999 Jan;9(1):19-27. doi: 10.1016/s0960-8966(98)00094-7. Neuromuscul Disord. 1999. PMID: 10063831

We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob MD, Day JW. Nat Genet 1998;19:196-198]. The genetically distinct form of myotonic dystrophy in the MN1 kindred shares some of …

We have recently mapped the disease locus (DM2) in this family to a 10 cM region of chromosome 3q [Ranum LPW, Rasmussen PF, Benzow KA, Koob …

5

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).

Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, Ranum LP. Koob MD, et al. Among authors: day jw. Nat Genet. 1999 Apr;21(4):379-84. doi: 10.1038/7710. Nat Genet. 1999. PMID: 10192387

6

SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance.

Moseley ML, Schut LJ, Bird TD, Koob MD, Day JW, Ranum LP. Moseley ML, et al. Among authors: day jw. Hum Mol Genet. 2000 Sep 1;9(14):2125-30. doi: 10.1093/hmg/9.14.2125. Hum Mol Genet. 2000. PMID: 10958651

7

Spinocerebellar ataxia type 8: clinical features in a large family.

Day JW, Schut LJ, Moseley ML, Durand AC, Ranum LP. Day JW, et al. Neurology. 2000 Sep 12;55(5):649-57. doi: 10.1212/wnl.55.5.649. Neurology. 2000. PMID: 10980728

8

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9.

Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. Liquori CL, et al. Among authors: day jw. Science. 2001 Aug 3;293(5531):864-7. doi: 10.1126/science.1062125. Science. 2001. PMID: 11486088

9

Dominantly inherited, non-coding microsatellite expansion disorders.

Ranum LP, Day JW. Ranum LP, et al. Among authors: day jw. Curr Opin Genet Dev. 2002 Jun;12(3):266-71. doi: 10.1016/s0959-437x(02)00297-6. Curr Opin Genet Dev. 2002. PMID: 12076668 Review.

10

Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.

Ranum LP, Day JW. Ranum LP, et al. Among authors: day jw. Curr Neurol Neurosci Rep. 2002 Sep;2(5):465-70. doi: 10.1007/s11910-002-0074-6. Curr Neurol Neurosci Rep. 2002. PMID: 12169228 Review.

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