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Novel and highly recurrent chromosomal alterations in SÃ©zary syndrome

ChEBI2010-05-18 更新2026-07-21 收录

皮肤T细胞淋巴瘤基因组学

染色体异常

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-16384 数据链接链接失效反馈

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资源简介：

Novel and highly recurrent chromosomal alterations in SÃ©zary syndrome

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创建时间：

2010-05-18

胎儿发育

染色体异常

This dataset contains data used for analysis in this paper as excel sheets. Also contains tables of statistical analysis and a few examples of images wherein the measurements were obtained.

DataCite Commons2021-04-12 更新80

Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells. Homo sapiens

细胞基因组不稳定性

染色体异常

array-CGH analysis of human neural stem cells derived from human ES cells during long term in vitro culture Overall design: array-CGH analysis of human neural stem cells derived from human ES cells co

NIAID Data Ecosystem50

Comparison of clinical outcomes from baseline analysis of the two screening approaches in a general screening population.

筛查评估

染色体异常

NIPT, non-invasive prenatal testing * 70% of total affected pregnancies (30% receive no screening). † Assuming termination rates for trisomy 21, trisomy 18, trisomy 13, and monosomy X of 87%, 81%, 90%

NIAID Data Ecosystem40

The Mutational Landscape of CTCL and Sezary Syndrome.

皮肤T细胞淋巴瘤基因组学

肿瘤靶向治疗遗传标记

Sezary syndrome is a leukemic and aggressive form of cutaneous T-cell lymphoma (CTCL) resulting from the malignant transformation of skin-homing central memory CD4+ T cells. To identify new genetic al

NIAID Data Ecosystem60

Summary of individuals with isolated 1p36 deletions and cardiovascular malformations identified from the DECIPHER database.

染色体异常

血管畸形

= Deletion defines a cardiac critical region.

Figshare2015-12-02 更新50