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A heterozygous protein‐truncating RFX6 variant in a family with childhood‐onset, pregnancy‐associated and adult‐onset diabetes

Diabetic medicine, 2020-10, Vol.37 (10), p.1772-1776

2020

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Catastrophic cellular events leading to complex chromosomal rearrangements in the germline

Clinical genetics, 2017-05, Vol.91 (5), p.653-660

2017

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Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool

Human reproduction (Oxford), 2019-09, Vol.34 (9), p.1762-1769

2019

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Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients

Human reproduction (Oxford), 2015-03, Vol.30 (3), p.499-506

2015

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All-Optical Cryogenic Thermometry Based on Nitrogen-Vacancy Centers in Nanodiamonds

Physical review applied, 2019-07, Vol.12 (1), Article 014042

2019

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Protein‐altering variants of PTPN2 in childhood‐onset Type 1A diabetes

Diabetic medicine, 2018-03, Vol.35 (3), p.376-380

2018

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First Report of Grapevine Algerian latent virus Infection on Alstroemeria spp. in Japan

Plant disease, 2016-06, Vol.100 (6), p.1251-1251

2016

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Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes

Diabetic medicine, 2020-12, Vol.37 (12), p.2131-2135

2020

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Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)mat

Clinical genetics, 2016-05, Vol.89 (5), p.614-619

2016

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Next‐generation sequencing for patients with non‐obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations

Andrology (Oxford), 2017-07, Vol.5 (4), p.824-831

2017

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Copy number variations in the amylase gene (AMY2B) in Japanese native dog breeds

Animal genetics, 2015-10, Vol.46 (5), p.580-583

2015

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FUT2 non‐secretor status is associated with Type 1 diabetes susceptibility in Japanese children

Diabetic medicine, 2017-04, Vol.34 (4), p.586-589

2017

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Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21

Diabetic medicine, 2016-12, Vol.33 (12), p.1717-1722

2016

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The Hippocampal Cholinergic Neurostimulating Peptide, the N-terminal Fragment of the Secreted Phosphatidylethanolamine-binding Protein, Possesses a New Biological Activity on Cardiac Physiology

The Journal of biological chemistry, 2004-03, Vol.279 (13), p.13054-13064

2004

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Genomic variation in the azf region associated with the risk of azoospermia

Fertility and sterility, 2014-09, Vol.102 (3), p.e350-e350

2014

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Polymorphisms of MAMLD1 gene in hypospadias

Journal of pediatric urology, 2011-12, Vol.7 (6), p.585-591

2011

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Macular Hole Surgery as a Historical Perspective

Clinical ophthalmology (Auckland, N.Z.), 2024-07, Vol.18, p.1981-1989

2024

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A heterozygous protein‐truncating RFX 6 variant in a family with childhood‐onset, pregnancy‐associated and adult‐onset diabetes

Diabetic medicine, 2020-10, Vol.37 (10), p.1772-1776

2020

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MAMLD1 (CXorf6): A New Gene for Hypospadias

Sexual development, 2008-01, Vol.2 (4-5), p.244-250

2008

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Genotypic differences in effects of cadmium on growth and nutrient compositions in wheat

Journal of plant nutrition, 2000-09, Vol.23 (9), p.1337-1350

2000

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Vitrectomy for macular edema due to retinal vein occlusion

Clinical ophthalmology (Auckland, N.Z.), 2019-06, Vol.13, p.969-984

2019

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Long-term outcomes of intravitreous bevacizumab or tissue plasminogen activator or vitrectomy for macular edema due to branch retinal vein occlusion

Clinical ophthalmology (Auckland, N.Z.), 2019-04, Vol.13, p.617-626

2019

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Influence of cadmium on mineral concentrations and yield components in wheat genotypes differing in Cd tolerance at seedling stage

Field crops research, 2002-09, Vol.77 (2), p.93-98

2002

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Rub epilepsy: a somatosensory evoked reflex epilepsy induced by prolonged cutaneous stimulation

Journal of neurology, neurosurgery and psychiatry, 2001-04, Vol.70 (4), p.541-543

2001

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A heterozygous protein‐truncating RFX6 variant in a family with childhood‐onset, pregnancy‐associated and adult‐onset diabetes

Catastrophic cellular events leading to complex chromosomal rearrangements in the germline

Aneuploid rescue precedes X-chromosome inactivation and increases the incidence of its skewness by reducing the size of the embryonic progenitor cell pool

Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients

All-Optical Cryogenic Thermometry Based on Nitrogen-Vacancy Centers in Nanodiamonds

Protein‐altering variants of PTPN2 in childhood‐onset Type 1A diabetes

First Report of Grapevine Algerian latent virus Infection on Alstroemeria spp. in Japan

Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes

Risk assessment of medically assisted reproduction and advanced maternal ages in the development of Prader-Willi syndrome due to UPD(15)mat

Next‐generation sequencing for patients with non‐obstructive azoospermia: implications for significant roles of monogenic/oligogenic mutations

Construction of an integrated high density simple sequence repeat linkage map in cultivated strawberry (Fragaria × ananassa) and its applicability

Copy number variations in the amylase gene (AMY2B) in Japanese native dog breeds

FUT2 non‐secretor status is associated with Type 1 diabetes susceptibility in Japanese children

Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21

The Hippocampal Cholinergic Neurostimulating Peptide, the N-terminal Fragment of the Secreted Phosphatidylethanolamine-binding Protein, Possesses a New Biological Activity on Cardiac Physiology

Genomic variation in the azf region associated with the risk of azoospermia

Polymorphisms of MAMLD1 gene in hypospadias

Macular Hole Surgery as a Historical Perspective

A heterozygous protein‐truncating RFX 6 variant in a family with childhood‐onset, pregnancy‐associated and adult‐onset diabetes

MAMLD1 (CXorf6): A New Gene for Hypospadias

Genotypic differences in effects of cadmium on growth and nutrient compositions in wheat

Vitrectomy for macular edema due to retinal vein occlusion

Long-term outcomes of intravitreous bevacizumab or tissue plasminogen activator or vitrectomy for macular edema due to branch retinal vein occlusion

Influence of cadmium on mineral concentrations and yield components in wheat genotypes differing in Cd tolerance at seedling stage

Rub epilepsy: a somatosensory evoked reflex epilepsy induced by prolonged cutaneous stimulation

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