米国のヒトゲノムプロジェクトのための新しい5年計画.

Pulmonary Artery Stenting for Widespread Distal Congenital Stenoses.

JACC. Case reports·2025

Replacing fishmeal with plant protein in Atlantic salmon (Salmo salar) diets by supplementation with fish protein hydrolysate.

Scientific reports·2020

Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrum.

Clinical genetics·2015

Report on a clinical evaluation of the KerraPro Heel silicone heel pad.

Journal of wound care·2013

Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome.

Clinical genetics·2013

Towards predictive stochastic dynamical modeling of cancer genesis and progression.

Interdisciplinary sciences, computational life sciences·2010

Antibodies sculpt adult brain circuits.

Science (New York, N.Y.)·2026

Ice as a geochemical reactor.

Science (New York, N.Y.)·2026

To eat or to breathe?

Science (New York, N.Y.)·2026

Roots navigate around decay regions by sensing local pH gradients.

Science (New York, N.Y.)·2026

In Science Journals.

Science (New York, N.Y.)·2026

Transient assembly of precision-tuned platinum-skin intermetallic catalysts for fuel cells.

Science (New York, N.Y.)·2026

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 FN1 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

関連する実験動画

米国のヒトゲノムプロジェクトのための新しい5年計画

関連する概念動画

Pulmonary Artery Stenting for Widespread Distal Congenital Stenoses.

Replacing fishmeal with plant protein in Atlantic salmon (Salmo salar) diets by supplementation with fish protein hydrolysate.

Congenital generalized lipodystrophy: identification of novel variants and expansion of clinical spectrum.

Report on a clinical evaluation of the KerraPro Heel silicone heel pad.

Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome.

Towards predictive stochastic dynamical modeling of cancer genesis and progression.

Antibodies sculpt adult brain circuits.

Ice as a geochemical reactor.

To eat or to breathe?

Roots navigate around decay regions by sensing local pH gradients.

In Science Journals.

Transient assembly of precision-tuned platinum-skin intermetallic catalysts for fuel cells.

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 FN1 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.

関連する実験動画

米国のヒトゲノムプロジェクトのための新しい5年計画

関連する概念動画

関連記事