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Additional file 2 of Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

NIAID Data Ecosystem2026-05-01 收录

22q11.2缺失综合征

疾病分子通路研究

数据链接：

https://figshare.com/articles/dataset/Additional_file_2_of_Exploring_pathway_interactions_to_detect_molecular_mechanisms_of_disease_22q11_2_deletion_syndrome/24425829 数据链接链接失效反馈

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资源简介：

Supplementary Material 2

应用场景：

创建时间：

2023-10-24

先天性心脏病

22q11.2缺失综合征

Abstract Congenital heart defects are the most common birth defects and the leading cause of mortality in the first year of life. It is well known that the 22q11 deletion syndrome (22q11DS) is the mos

DataCite Commons2020-08-26 更新120

Evaluation of an online mindfulness training for adolescents with 22q11.2 Deletion Syndrome

22q11.2缺失综合征

正念干预

The goal of this study was to evaluate the effectiveness of the Aware Program, an online mindfulness education program, with adolescents (aged 12-19 years) with 22q11.2 Deletion Syndrome and one of th

DataCite Commons2024-11-29 更新50

Whole Genome Sequencing of Two Family Trios with 22q.11.2 Deletion Syndrome

22q11.2缺失综合征

遗传修饰因子识别

Two subjects with 22q11.2 deletion syndromes (22q11DS) and their parents were recruited for a whole genome sequencing study to identify candidate genetic modifiers of the various phenotypes seen in 22

NIAID Data Ecosystem30

Evaluation of an online mindfulness training for adolescents with 22q11.2 Deletion Syndrome

心理健康干预

22q11.2缺失综合征

DataCite Commons2024-11-29 更新90

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

精神分裂症遗传易感性

22q11.2缺失综合征

The location of a schizophrenia susceptibility locus at chromosome 22q11 has been suggested by genome-wide linkage studies. Additional support was provided by the observation of a higher-than-expected

PubMed Central2002-03-12 更新40

Additional file 2 of Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

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