• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Biallelic mutations in cause Shwachman-Diamond syndrome.

作者信息

Dhanraj Santhosh, Matveev Anna, Li Hongbing, Lauhasurayotin Supanun, Jardine Lawrence, Cada Michaela, Zlateska Bozana, Tailor Chetankumar S, Zhou Joseph, Mendoza-Londono Roberto, Vincent Ajoy, Durie Peter R, Scherer Stephen W, Rommens Johanna M, Heon Elise, Dror Yigal

机构信息

Program in Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.

Institute of Medical Science, University of Toronto, Toronto, ON, Canada.

出版信息

Blood. 2017 Mar 16;129(11):1557-1562. doi: 10.1182/blood-2016-08-735431. Epub 2017 Jan 6.

DOI:10.1182/blood-2016-08-735431
PMID:28062395
Abstract
摘要

相似文献

1
Biallelic mutations in cause Shwachman-Diamond syndrome.[基因名称]的双等位基因突变导致施瓦赫曼-戴蒙德综合征。 (这里原文中“in”后面缺少具体基因名称,所以翻译只能到这个程度,需补充完整基因信息才能准确翻译全句)
Blood. 2017 Mar 16;129(11):1557-1562. doi: 10.1182/blood-2016-08-735431. Epub 2017 Jan 6.
2
A novel missense mutation outside the DNAJ domain of DNAJC21 is associated with Shwachman-Diamond syndrome.DNAJC21的DNAJ结构域之外的一种新型错义突变与施-戴二氏综合征相关。
Br J Haematol. 2022 Jun;197(6):e88-e93. doi: 10.1111/bjh.18112. Epub 2022 Mar 17.
3
Refining the phenotype associated with biallelic DNAJC21 mutations.细化与双等位基因突变相关的表型。
Clin Genet. 2018 Aug;94(2):252-258. doi: 10.1111/cge.13370. Epub 2018 Jun 7.
4
[Pediatric Shwachman-diamond syndrome: report on 5 cases and literature review].[小儿施瓦赫曼-戴蒙德综合征:5例报告及文献复习]
Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):970-4.
5
Breast cancer in a case of Shwachman Diamond syndrome.一例 Shwachman Diamond 综合征相关乳腺癌。
Pediatr Blood Cancer. 2012 Nov;59(5):945-6. doi: 10.1002/pbc.24052. Epub 2011 Dec 27.
6
Absence of SBDS mutations in sporadic paediatric acute myeloid leukaemia.散发性小儿急性髓细胞白血病中无SBDS突变
Br J Haematol. 2013 Feb;160(4):559-61. doi: 10.1111/bjh.12134. Epub 2012 Nov 28.
7
Shwachman-Diamond syndrome in India.印度的施瓦赫曼-戴蒙德综合征。
Pediatr Blood Cancer. 2012 Mar;58(3):479-80. doi: 10.1002/pbc.23332. Epub 2011 Oct 11.
8
Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives.Shwachman-Diamond 综合征:分子机制与研究现状。
Mol Diagn Ther. 2019 Apr;23(2):281-290. doi: 10.1007/s40291-018-0368-2.
9
The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data.希腊舒-戴综合征注册登记处:分子与临床数据。
Pediatr Blood Cancer. 2017 Nov;64(11). doi: 10.1002/pbc.26630. Epub 2017 May 16.
10
Dysplastic neutrophils in the bone marrow of a Shwachman-Diamond syndrome patient.一名施瓦茨曼-戴蒙德综合征患者骨髓中的发育异常中性粒细胞。
Blood. 2017 Jul 6;130(1):96. doi: 10.1182/blood-2017-03-773846.

引用本文的文献

1
Structural Implications of Missense Point Mutations in Shwachman-Bodian-Diamond Syndrome Protein (SBDS): A Combined SAXS/MD Investigation.施瓦赫曼-博迪安-戴蒙德综合征蛋白(SBDS)中错义点突变的结构影响:小角X射线散射/分子动力学联合研究
ACS Omega. 2025 Aug 1;10(31):35103-35118. doi: 10.1021/acsomega.5c04764. eCollection 2025 Aug 12.
2
Adult presentation of Shwachman-Diamond syndrome complicated by liver cirrhosis and pancreatic fat infiltration: A case report.成人期呈现的施瓦赫曼-戴蒙德综合征合并肝硬化及胰腺脂肪浸润:一例报告
World J Hepatol. 2025 Jun 27;17(6):108558. doi: 10.4254/wjh.v17.i6.108558.
3
Clinical characteristics and genetic mutation analysis in 18 pediatric patients with Shwachman-Diamond syndrome.
18例施瓦赫曼-戴蒙德综合征患儿的临床特征及基因突变分析
Front Genet. 2025 Jun 18;16:1603782. doi: 10.3389/fgene.2025.1603782. eCollection 2025.
4
Emerging roles of ribosome translation in stem cells and stem cell therapy - a review.核糖体翻译在干细胞及干细胞治疗中的新作用——综述
Cell Biosci. 2025 May 28;15(1):71. doi: 10.1186/s13578-025-01412-y.
5
Shwachman-Diamond syndrome due to biallelic EFL1 variants with complex and fatal clinical course in early infancy.双等位基因EFL1变异导致的舒-戴综合征,在婴儿早期临床病程复杂且致命。
Br J Haematol. 2024 Dec;205(6):2363-2369. doi: 10.1111/bjh.19793. Epub 2024 Oct 8.
6
Inherited Predispositions to Myeloid Neoplasms: Pathogenesis and Clinical Implications.髓系肿瘤的遗传易感性:发病机制与临床意义
Annu Rev Pathol. 2025 Jan;20(1):87-114. doi: 10.1146/annurev-pathmechdis-111523-023420. Epub 2025 Jan 2.
7
[Allogeneic hematopoietic stem cell transplantation for Shwachman-Diamond syndrome: a report of three cases and literature review].[异基因造血干细胞移植治疗施瓦茨曼-戴蒙德综合征:三例报告及文献复习]
Zhonghua Xue Ye Xue Za Zhi. 2024 Jul 14;45(7):689-693. doi: 10.3760/cma.j.cn121090-20240107-00009.
8
Loss of Dnajc21 leads to cytopenia and altered nucleotide metabolism in zebrafish.DNajC21 的缺失导致斑马鱼血细胞减少和核苷酸代谢改变。
Leukemia. 2024 Oct;38(10):2115-2126. doi: 10.1038/s41375-024-02367-8. Epub 2024 Aug 13.
9
Lethal Complications and Complex Genotypes in Shwachman Diamond Syndrome: Report of a Family with Recurrent Neonatal Deaths and a Case-Based Brief Review of the Literature.施瓦赫曼-戴蒙德综合征的致命并发症与复杂基因型:一个有反复新生儿死亡病例的家族报告及基于病例的文献简要综述
Children (Basel). 2024 Jun 7;11(6):705. doi: 10.3390/children11060705.
10
A naturally occurring canine model of syndromic congenital microphthalmia.一种综合征型先天性小眼球的天然发生犬模型。
G3 (Bethesda). 2024 Jun 5;14(6). doi: 10.1093/g3journal/jkae067.