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Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis

Journal of human genetics, 2016-07, Vol.61 (7), p.585-591

2016

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Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature

Journal of human genetics, 2015-09, Vol.60 (9), p.553-556

2015

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The Phase Structure of the Gross-Neveu Model with Thirring Interaction at the Next-to-Leading Order of the 1/N Expansion

Progress of theoretical physics, 1997-06, Vol.97 (6), p.921-937

Dateki, T.

1997

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MLD-Based MU-MIMO Detection Scheme for LTE Downlink

2012 IEEE 75th Vehicular Technology Conference (VTC Spring), 2012, p.1-5

2012

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New OFDM Channel Estimation Method by Adding a Virtual Channel Frequency Response

IEEE Vehicular Technology Conference, 2006, p.1-5

2006

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Evaluation of New NLMS and RLS Chip Equalizers using Tentative Decision Data for HSDPA Systems

2006 IEEE 63rd Vehicular Technology Conference, 2006, Vol.5, p.2429-2433

2006

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ACAN mutations as a cause of familial short stature

Clinical Pediatric Endocrinology, 2017, Vol.26(3), pp.119-125

Dateki, Sumito

2017

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RAN Slicing with Inter-Cell Interference Control and Link Adaptation for Reliable Wireless Communications

IEICE transactions on communications, 2024-07, Vol.E107-B (7), p.513-528

2024

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Donepezil‐induced oligodendrocyte differentiation is mediated through estrogen receptors

Journal of neurochemistry, 2020-12, Vol.155 (5), p.494-507

2020

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High allele discrimination in the typing of single nucleotide polymorphisms of miRNA

Bioorganic & medicinal chemistry, 2021-09, Vol.46, p.116363-116363, Article 116363

2021

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Neuronal Ca2+‐dependent activator protein 1 (NCDAP1) induces neuronal cell death by activating p53 pathway following traumatic brain injury

Journal of neurochemistry, 2019-12, Vol.151 (6), p.795-809

2019

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Identification of a novel heterozygous mutation of the Aggrecan gene in a family with idiopathic short stature and multiple intervertebral disc herniation

Journal of human genetics, 2017-07, Vol.62 (7), p.717-721

2017

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A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency

Journal of human genetics, 2019-04, Vol.64 (4), p.341-346

2019

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Nicotinic acetylcholine receptors mediate donepezil‐induced oligodendrocyte differentiation

Journal of neurochemistry, 2015-12, Vol.135 (6), p.1086-1098

2015

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A novel strategy of selective gene delivery by using a uniform magnetic field

Biotechnology journal, 2021-04, Vol.16 (4), p.e2000233-n/a

2021

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NF-κB plays an important role in indoxyl sulfate-induced cellular senescence, fibrotic gene expression, and inhibition of proliferation in proximal tubular cells

American Journal of Physiology: Cell Physiology, 2011-11, Vol.301 (5), p.C1201-C1212

2011

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Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Endocrine Journal, 2017, Vol.64(10), pp.947-954

2017

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Neuronal Ca 2+ -dependent activator protein 1 (NCDAP1) induces neuronal cell death by activating p53 pathway following traumatic brain injury

Journal of neurochemistry, 2019-12, Vol.151 (6), p.795-809

2019

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Donepezil promotes differentiation of neural stem cells into mature oligodendrocytes at the expense of astrogenesis

Journal of neurochemistry, 2017-01, Vol.140 (2), p.231-244

2017

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Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome

Journal of human genetics, 2019-05, Vol.64 (5), p.467-471

2019

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A case of ezetimibe-effective hypercholesterolemia with a novel heterozygous variant in ABCG5

Endocrine Journal, 2020, Vol.67(11), pp.1099-1105

2020

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An Iron-chelating Agent Improved the Cardiac Function in a Patient with Severe Heart Failure Due to Hereditary Hemochromatosis

Internal Medicine, 2024/01/15, Vol.63(2), pp.253-258

2024

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A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome

Journal of human genetics, 2018-03, Vol.63 (3), p.387-390

2018

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A novel strategy for selective gene delivery by using the inhibitory effect of blue light on jetPRIME-mediated transfection

Biotechnology and bioengineering, 2016-07, Vol.113 (7), p.1560-1567

2016

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Numerous intertriginous xanthomas in infant: A diagnostic clue for sitosterolemia

Journal of dermatology, 2016-11, Vol.43 (11), p.1340-1344

2016

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Systematic molecular analyses of SHOX in Japanese patients with idiopathic short stature and Leri-Weill dyschondrosteosis

Rare pseudoautosomal copy-number variations involving SHOX and/or its flanking regions in individuals with and without short stature

The Phase Structure of the Gross-Neveu Model with Thirring Interaction at the Next-to-Leading Order of the 1/N Expansion

MLD-Based MU-MIMO Detection Scheme for LTE Downlink

New OFDM Channel Estimation Method by Adding a Virtual Channel Frequency Response

Evaluation of New NLMS and RLS Chip Equalizers using Tentative Decision Data for HSDPA Systems

ACAN mutations as a cause of familial short stature

RAN Slicing with Inter-Cell Interference Control and Link Adaptation for Reliable Wireless Communications

Donepezil‐induced oligodendrocyte differentiation is mediated through estrogen receptors

High allele discrimination in the typing of single nucleotide polymorphisms of miRNA

Neuronal Ca2+‐dependent activator protein 1 (NCDAP1) induces neuronal cell death by activating p53 pathway following traumatic brain injury

Identification of a novel heterozygous mutation of the Aggrecan gene in a family with idiopathic short stature and multiple intervertebral disc herniation

A homozygous splice site ROBO1 mutation in a patient with a novel syndrome with combined pituitary hormone deficiency

Nicotinic acetylcholine receptors mediate donepezil‐induced oligodendrocyte differentiation

A novel strategy of selective gene delivery by using a uniform magnetic field

NF-κB plays an important role in indoxyl sulfate-induced cellular senescence, fibrotic gene expression, and inhibition of proliferation in proximal tubular cells

Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Neuronal Ca 2+ -dependent activator protein 1 (NCDAP1) induces neuronal cell death by activating p53 pathway following traumatic brain injury

Donepezil promotes differentiation of neural stem cells into mature oligodendrocytes at the expense of astrogenesis

Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome

A case of ezetimibe-effective hypercholesterolemia with a novel heterozygous variant in ABCG5

An Iron-chelating Agent Improved the Cardiac Function in a Patient with Severe Heart Failure Due to Hereditary Hemochromatosis

A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome

A novel strategy for selective gene delivery by using the inhibitory effect of blue light on jetPRIME-mediated transfection

Numerous intertriginous xanthomas in infant: A diagnostic clue for sitosterolemia

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