[Models for vulnerability and liability of schizophrenia--heredity, environment, and their interaction]

Summer carbon budget simulation in a lagoon ecosystem with submerged aquatic vegetation.

The Science of the total environment·2026

Demonstration of nuclear gamma-ray polarimetry based on a multi-layer CdTe Compton camera.

Scientific reports·2024

High-power laser experiment forming a supercritical collisionless shock in a magnetized uniform plasma at rest.

Physical review. E·2022

Sign of Hard-X-Ray Pulsation from the γ-Ray Binary System LS 5039.

Physical review letters·2020

A very-high-energy component deep in the γ-ray burst afterglow.

Nature·2019

Thumb boutonnière deformity without rheumatoid arthritis or trauma.

The Journal of hand surgery, European volume·2017

[The Current Issues of Crime Victim Support from a Clinical Point of View].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[The Role of Psychiatrists as Personal Support Specialists].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[Historical Re-evaluation of the System of Sending Psychiatrists to Okinawa and the Activities of the Japanese Society of Psychiatry and Neurology].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[Background of Okinawa's Acceptance of Dispatched Physicians and Its Current Status].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[Medical Dispatch to Okinawa and following Period].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[The Situation of Psychiatric Medicine and the System of Dispatching Medical Doctors Half a Century Ago in Okinawa].

Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica·2019

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

[Models for vulnerability and liability of schizophrenia--heredity, environment, and their interaction]

Related Concept Videos

Summer carbon budget simulation in a lagoon ecosystem with submerged aquatic vegetation.

Demonstration of nuclear gamma-ray polarimetry based on a multi-layer CdTe Compton camera.

High-power laser experiment forming a supercritical collisionless shock in a magnetized uniform plasma at rest.

Sign of Hard-X-Ray Pulsation from the γ-Ray Binary System LS 5039.

A very-high-energy component deep in the γ-ray burst afterglow.

Thumb boutonnière deformity without rheumatoid arthritis or trauma.

[The Current Issues of Crime Victim Support from a Clinical Point of View].

[The Role of Psychiatrists as Personal Support Specialists].

[Historical Re-evaluation of the System of Sending Psychiatrists to Okinawa and the Activities of the Japanese Society of Psychiatry and Neurology].

[Background of Okinawa's Acceptance of Dispatched Physicians and Its Current Status].

[Medical Dispatch to Okinawa and following Period].

[The Situation of Psychiatric Medicine and the System of Dispatching Medical Doctors Half a Century Ago in Okinawa].

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Related Experiment Videos

[Models for vulnerability and liability of schizophrenia--heredity, environment, and their interaction]

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