Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

1,737 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
The FHA domain of aprataxin interacts with the C-terminal region of XRCC1.
Date H, Igarashi S, Sano Y, Takahashi T, Takahashi T, Takano H, Tsuji S, Nishizawa M, Onodera O. Date H, et al. Among authors: takano h. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1279-85. doi: 10.1016/j.bbrc.2004.10.162. Biochem Biophys Res Commun. 2004. PMID: 15555565
Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.
Matsukawa T, Asheuer M, Takahashi Y, Goto J, Suzuki Y, Shimozawa N, Takano H, Onodera O, Nishizawa M, Aubourg P, Tsuji S. Matsukawa T, et al. Among authors: takano h. Neurogenetics. 2011 Feb;12(1):41-50. doi: 10.1007/s10048-010-0253-6. Epub 2010 Jul 27. Neurogenetics. 2011. PMID: 20661612 Free PMC article.
Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.
Sato A, Shimohata T, Koide R, Takano H, Sato T, Oyake M, Igarashi S, Tanaka K, Inuzuka T, Nawa H, Tsuji S. Sato A, et al. Among authors: takano h. Hum Mol Genet. 1999 Jun;8(6):997-1006. doi: 10.1093/hmg/8.6.997. Hum Mol Genet. 1999. PMID: 10332031
No mutation in the entire coding region of the alpha-synuclein gene in pathologically confirmed cases of multiple system atrophy.
Ozawa T, Takano H, Onodera O, Kobayashi H, Ikeuchi T, Koide R, Okuizumi K, Shimohata T, Wakabayashi K, Takahashi H, Tsuji S. Ozawa T, et al. Among authors: takano h. Neurosci Lett. 1999 Jul 30;270(2):110-2. doi: 10.1016/s0304-3940(99)00475-9. Neurosci Lett. 1999. PMID: 10462110
Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmission.
Shimohata T, Ishiguro H, Makino K, Takano H, Tanaka H, Tsuji S, Hirota K. Shimohata T, et al. Among authors: takano h. Neurology. 1998 Jan;50(1):282-3. doi: 10.1212/wnl.50.1.282. Neurology. 1998. PMID: 9443494
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
Ikeuchi T, Sanpei K, Takano H, Sasaki H, Tashiro K, Cancel G, Brice A, Bird TD, Schellenberg GD, Pericak-Vance MA, Welsh-Bohmer KA, Clark LN, Wilhelmsen K, Tsuji S. Ikeuchi T, et al. Among authors: takano h. Genomics. 1998 Apr 15;49(2):321-6. doi: 10.1006/geno.1998.5266. Genomics. 1998. PMID: 9598323
Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.
Onodera O, Idezuka J, Igarashi S, Takiyama Y, Endo K, Takano H, Oyake M, Tanaka H, Inuzuka T, Hayashi T, Yuasa T, Ito J, Miyatake T, Tsuji S. Onodera O, et al. Among authors: takano h. Ann Neurol. 1998 Mar;43(3):288-96. doi: 10.1002/ana.410430305. Ann Neurol. 1998. PMID: 9506544
1,737 results
Jump to page
Feedback