[Familial occurrence of Basedow's disease]

Search for Dark Particles in K_{L}^{0}→γX at the KOTO Experiment.

Physical review letters·2026

Search for the K_{L}→π^{0}νν[over ¯] Decay at the J-PARC KOTO Experiment.

Physical review letters·2025

Search for the Pair Production of Dark Particles X with K_{L}^{0}→XX, X→γγ.

Physical review letters·2023

Study of the K_{L}→π^{0}νν[over ¯] Decay at the J-PARC KOTO Experiment.

Physical review letters·2021

Toward High Precision XCO<sub>2</sub> Retrievals From TanSat Observations: Retrieval Improvement and Validation Against TCCON Measurements.

Journal of geophysical research. Atmospheres : JGR·2021

Search for K_{L}→π^{0}νν[over ¯] and K_{L}→π^{0}X^{0} Decays at the J-PARC KOTO Experiment.

Physical review letters·2019

[The significance of platelet alpha 2-adrenoceptor and sympathetic nerve activity in the hypertensive mechanism under essential hypertension--with special reference to pressor response to norepinephrine].

Nihon Naibunpi Gakkai zasshi·1995

[Mechanism of inhibition of aldosterone secretion by a Ca2+ channel blocker in patients with essential hypertension and patients with primary aldosteronism].

Nihon Naibunpi Gakkai zasshi·1995

[The future of the Japan Endocrine Society].

Nihon Naibunpi Gakkai zasshi·1995

[Comment by a surgeon on Japan Endocrine Society, its past and future].

Nihon Naibunpi Gakkai zasshi·1995

[A view of basic endocrinology].

Nihon Naibunpi Gakkai zasshi·1995

[Treatment of hypothalamic-pituitary tumors--experiences at Hiroshima University School of Medicine].

Nihon Naibunpi Gakkai zasshi·1995

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

[Familial occurrence of Basedow's disease]

Related Concept Videos

Search for Dark Particles in K_{L}^{0}→γX at the KOTO Experiment.

Search for the K_{L}→π^{0}νν[over ¯] Decay at the J-PARC KOTO Experiment.

Search for the Pair Production of Dark Particles X with K_{L}^{0}→XX, X→γγ.

Study of the K_{L}→π^{0}νν[over ¯] Decay at the J-PARC KOTO Experiment.

Toward High Precision XCO<sub>2</sub> Retrievals From TanSat Observations: Retrieval Improvement and Validation Against TCCON Measurements.

Search for K_{L}→π^{0}νν[over ¯] and K_{L}→π^{0}X^{0} Decays at the J-PARC KOTO Experiment.

[The significance of platelet alpha 2-adrenoceptor and sympathetic nerve activity in the hypertensive mechanism under essential hypertension--with special reference to pressor response to norepinephrine].

[Mechanism of inhibition of aldosterone secretion by a Ca2+ channel blocker in patients with essential hypertension and patients with primary aldosteronism].

[The future of the Japan Endocrine Society].

[Comment by a surgeon on Japan Endocrine Society, its past and future].

[A view of basic endocrinology].

[Treatment of hypothalamic-pituitary tumors--experiences at Hiroshima University School of Medicine].

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Related Experiment Videos

[Familial occurrence of Basedow's disease]

Related Concept Videos

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