Kato T - Search Results

1

Copy number loss in SFMBT1 is common among Finnish and Norwegian patients with iNPH.

Korhonen VE, Helisalmi S, Jokinen A, Jokinen I, Lehtola JM, Oinas M, Lönnrot K, Avellan C, Kotkansalo A, Frantzen J, Rinne J, Ronkainen A, Kauppinen M, Junkkari A, Hiltunen M, Soininen H, Kurki M, Jääskeläinen JE, Koivisto AM, Sato H, Kato T, Remes AM, Eide PK, Leinonen V. Korhonen VE, et al. Among authors: kato t. Neurol Genet. 2018 Dec 3;4(6):e291. doi: 10.1212/NXG.0000000000000291. eCollection 2018 Dec. Neurol Genet. 2018. PMID: 30584596 Free PMC article.

2

Segmental copy number loss of SFMBT1 gene in elderly individuals with ventriculomegaly: a community-based study.

Kato T, Sato H, Emi M, Seino T, Arawaka S, Iseki C, Takahashi Y, Wada M, Kawanami T. Kato T, et al. Intern Med. 2011;50(4):297-303. doi: 10.2169/internalmedicine.50.4505. Epub 2011 Feb 15. Intern Med. 2011. PMID: 21325761 Free article.

3

[iNPH (Idiopathic normal pressure hydrocephalus) and AVIM (asymptomatic ventriculomegaly with features of iNPH on MRI)].

Kato T, Iseki C, Takahashi Y, Wada M, Kawanami T, Sato H, Emi M. Kato T, et al. Rinsho Shinkeigaku. 2010 Nov;50(11):963-5. Rinsho Shinkeigaku. 2010. PMID: 21921528 Japanese.

4

A Segmental Copy Number Loss of the SFMBT1 Gene Is a Genetic Risk for Shunt-Responsive, Idiopathic Normal Pressure Hydrocephalus (iNPH): A Case-Control Study.

Sato H, Takahashi Y, Kimihira L, Iseki C, Kato H, Suzuki Y, Igari R, Sato H, Koyama S, Arawaka S, Kawanami T, Miyajima M, Samejima N, Sato S, Kameda M, Yamada S, Kita D, Kaijima M, Date I, Sonoda Y, Kayama T, Kuwana N, Arai H, Kato T. Sato H, et al. Among authors: kato t, kato h. PLoS One. 2016 Nov 18;11(11):e0166615. doi: 10.1371/journal.pone.0166615. eCollection 2016. PLoS One. 2016. PMID: 27861535 Free PMC article.

5

Midnolin is a confirmed genetic risk factor for Parkinson's disease.

Obara Y, Sato H, Nakayama T, Kato T, Ishii K. Obara Y, et al. Among authors: kato t. Ann Clin Transl Neurol. 2019 Nov;6(11):2205-2211. doi: 10.1002/acn3.50914. Epub 2019 Oct 6. Ann Clin Transl Neurol. 2019. PMID: 31588691 Free PMC article.

6

Impact of nocturnal heart rate variability on cerebral small-vessel disease progression: a longitudinal study in community-dwelling elderly Japanese.

Yamaguchi Y, Wada M, Sato H, Nagasawa H, Koyama S, Takahashi Y, Kawanami T, Kato T. Yamaguchi Y, et al. Among authors: kato t. Hypertens Res. 2015 Aug;38(8):564-9. doi: 10.1038/hr.2015.38. Epub 2015 Mar 19. Hypertens Res. 2015. PMID: 25787037

7

Whole-exome sequencing and digital PCR identified a novel compound heterozygous mutation in the NPHP1 gene in a case of Joubert syndrome and related disorders.

Koyama S, Sato H, Wada M, Kawanami T, Emi M, Kato T. Koyama S, et al. Among authors: kato t. BMC Med Genet. 2017 Mar 27;18(1):37. doi: 10.1186/s12881-017-0399-2. BMC Med Genet. 2017. PMID: 28347285 Free PMC article.

8

Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease.

Obara Y, Imai T, Sato H, Takeda Y, Kato T, Ishii K. Obara Y, et al. Among authors: kato t. Sci Rep. 2017 Jul 19;7(1):5885. doi: 10.1038/s41598-017-05456-0. Sci Rep. 2017. PMID: 28724963 Free PMC article.

9

Frequent genomic rearrangements of BRCA1 associated protein-1 (BAP1) gene in Japanese malignant mesothelioma-characterization of deletions at exon level.

Emi M, Yoshikawa Y, Sato C, Sato A, Sato H, Kato T, Tsujimura T, Hasegawa S, Nakano T, Hashimoto-Tamaoki T. Emi M, et al. Among authors: kato t. J Hum Genet. 2015 Oct;60(10):647-9. doi: 10.1038/jhg.2015.91. Epub 2015 Aug 6. J Hum Genet. 2015. PMID: 26246155

10

Segmental copy-number gain within the region of isopentenyl diphosphate isomerase genes in sporadic amyotrophic lateral sclerosis.

Kato T, Emi M, Sato H, Arawaka S, Wada M, Kawanami T, Katagiri T, Tsuburaya K, Toyoshima I, Tanaka F, Sobue G, Matsubara K. Kato T, et al. Biochem Biophys Res Commun. 2010 Nov 12;402(2):438-42. doi: 10.1016/j.bbrc.2010.10.056. Epub 2010 Oct 16. Biochem Biophys Res Commun. 2010. PMID: 20955688

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