Detalhe da pesquisa
1.
CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.
Am J Hum Genet
; 110(7): 1086-1097, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37339631
2.
Spectra and characteristics of somatic mutations induced by ionizing radiation in hematopoietic stem cells.
Proc Natl Acad Sci U S A
; 120(15): e2216550120, 2023 04 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37018193
3.
Kv11 (ether-à-go-go-related gene) voltage-dependent K+ channels promote resonance and oscillation of subthreshold membrane potentials.
J Physiol
; 599(2): 547-569, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33151574
4.
Optineurin regulates osteoblastogenesis through STAT1.
Biochem Biophys Res Commun
; 525(4): 889-894, 2020 05 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32171527
5.
Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.
BMC Med Genet
; 21(1): 68, 2020 03 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-32234020
6.
The first Japanese case of primary familial brain calcification caused by an MYORG variant.
J Hum Genet
; 65(10): 917-920, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32451491
7.
Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.
J Hum Genet
; 65(4): 363-369, 2020 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31907387
8.
Aggressive periodontitis and NOD2 variants.
J Hum Genet
; 65(10): 841-846, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32424308
9.
Ligand-Controlled Stereodivergent, Enantioselective Conjugate Addition of 2-Oxazoline- and 2-Thiazoline-4-carboxylate to Nitroalkene Catalyzed by Chiral Copper Complexes.
J Org Chem
; 81(17): 7939-7944, 2016 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27494779
10.
Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation.
J Neurol Neurosurg Psychiatry
; 91(2): 220-222, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31431468
11.
Radiopacity Measurement of Restorative Resins Using Film and Three Digital Systems for Comparison with ISO 4049: International Standard.
Bull Tokyo Dent Coll
; 56(4): 207-14, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657519
12.
Characteristic findings on panoramic radiography and cone-beam CT to predict paresthesia after extraction of impacted third molar.
Bull Tokyo Dent Coll
; 56(1): 1-8, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25765570
13.
Exposure time reduction of secondary radiographs used in digital subtraction radiography in detecting intrabony change.
Oral Radiol
; 30: 20-26, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24391352
14.
Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation.
Mov Disord Clin Pract
; 11(6): 720-727, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38605589
15.
Accessory mandibular foramina: a CT study of 300 cases.
Surg Radiol Anat
; 35(4): 323-30, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23192239
16.
A Basic Study for Predicting Dysphagia in Panoramic X-ray Images Using Artificial Intelligence (AI)-Part 1: Determining Evaluation Factors and Cutoff Levels.
Int J Environ Res Public Health
; 19(8)2022 04 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35457398
17.
Massive expansion of multiple clones in the mouse hematopoietic system long after whole-body X-irradiation.
Sci Rep
; 12(1): 17276, 2022 10 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-36241679
18.
Effect of computer assistance on observer performance of approximal caries diagnosis using intraoral digital radiography.
Clin Oral Investig
; 14(3): 319-25, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19557443
19.
Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel CaV3.1 caused by a mutation responsible for spinocerebellar ataxia.
Mol Brain
; 13(1): 163, 2020 11 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33243296
20.
Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.
Neurol Genet
; 6(1): e396, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32042923