结膜嗜酸性附属泪腺中的线粒体DNA突变。 - Suppr

Suppr

超能文献

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

作者信息

Bartoletti-Stella Anna, Salfi Nunzio C M, Ceccarelli Claudio, Attimonelli Marcella, Romeo Giovanni, Gasparre Giuseppe

出版信息

Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95.

DOI:10.1001/archophthalmol.2011.95

PMID:21555623

Abstract

摘要

相似文献

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95.

Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.

Cancer Res. 2006 Jun 15;66(12):6087-96. doi: 10.1158/0008-5472.CAN-06-0171.

Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.

Hum Mol Genet. 2008 Apr 1;17(7):986-95. doi: 10.1093/hmg/ddm371. Epub 2007 Dec 21.

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.

Hum Mutat. 2009 Mar;30(3):391-6. doi: 10.1002/humu.20870.

Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors.

Am J Pathol. 2002 May;160(5):1857-65. doi: 10.1016/S0002-9440(10)61132-7.

Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.

Clin Cancer Res. 2008 Apr 15;14(8):2270-5. doi: 10.1158/1078-0432.CCR-07-4131.

Oncocytic tumors are marked by enhanced mitochondrial content and mtDNA mutations of complex I in Chinese patients.

Mitochondrion. 2019 Mar;45:1-6. doi: 10.1016/j.mito.2018.01.008. Epub 2018 Jan 31.

Core I gene is overexpressed in Hürthle and non-Hürthle cell microfollicular adenomas and follicular carcinomas of the thyroid.

BMC Cancer. 2004 Mar 25;4:12. doi: 10.1186/1471-2407-4-12.

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

Proc Natl Acad Sci U S A. 2007 May 22;104(21):9001-6. doi: 10.1073/pnas.0703056104. Epub 2007 May 15.

[Analysis of mitochondrial DNA D-loop region mutation and its significance in human oncocytoma].

Zhonghua Zhong Liu Za Zhi. 2010 Oct;32(10):767-70.

引用本文的文献

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations.

Ann Clin Transl Neurol. 2024 Aug 2. doi: 10.1002/acn3.52141.

Rare Diseases of the Orbit.

Laryngorhinootologie. 2021 Apr;100(S 01):S1-S79. doi: 10.1055/a-1384-4641. Epub 2021 Apr 30.

Mitochondrial DNA variation and cancer.

Nat Rev Cancer. 2021 Jul;21(7):431-445. doi: 10.1038/s41568-021-00358-w. Epub 2021 May 27.

Mitochondrial somatic mutations and the lack of viral genomic variation in recurrent respiratory papillomatosis.

Sci Rep. 2019 Nov 12;9(1):16625. doi: 10.1038/s41598-019-53148-8.

Oncogenes, mitochondrial metabolism, and quality control in differentiated thyroid cancer.

Korean J Intern Med. 2017 Sep;32(5):780-789. doi: 10.3904/kjim.2016.420. Epub 2017 Aug 22.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells.

Cancer Metab. 2013 Mar 18;1(1):11. doi: 10.1186/2049-3002-1-11.

Relevance of mitochondrial genetics and metabolism in cancer development.

Cold Spring Harb Perspect Biol. 2013 Feb 1;5(2):a011411. doi: 10.1101/cshperspect.a011411.

Mitochondria and cancer.

Nat Rev Cancer. 2012 Oct;12(10):685-98. doi: 10.1038/nrc3365.

HmtDB, a genomic resource for mitochondrion-based human variability studies.

Nucleic Acids Res. 2012 Jan;40(Database issue):D1150-9. doi: 10.1093/nar/gkr1086. Epub 2011 Dec 1.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

作者信息

Bartoletti-Stella Anna, Salfi Nunzio C M, Ceccarelli Claudio, Attimonelli Marcella, Romeo Giovanni, Gasparre Giuseppe

出版信息

Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95.

DOI:10.1001/archophthalmol.2011.95

PMID:21555623

Abstract

摘要

相似文献

Mitochondrial DNA mutations in oncocytic adnexal lacrimal glands of the conjunctiva.

Arch Ophthalmol. 2011 May;129(5):664-6. doi: 10.1001/archophthalmol.2011.95.

Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.

Cancer Res. 2006 Jun 15;66(12):6087-96. doi: 10.1158/0008-5472.CAN-06-0171.

Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma.

Hum Mol Genet. 2008 Apr 1;17(7):986-95. doi: 10.1093/hmg/ddm371. Epub 2007 Dec 21.

An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells.

Hum Mutat. 2009 Mar;30(3):391-6. doi: 10.1002/humu.20870.

Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors.

Am J Pathol. 2002 May;160(5):1857-65. doi: 10.1016/S0002-9440(10)61132-7.

Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma.

Clin Cancer Res. 2008 Apr 15;14(8):2270-5. doi: 10.1158/1078-0432.CCR-07-4131.

Oncocytic tumors are marked by enhanced mitochondrial content and mtDNA mutations of complex I in Chinese patients.

Mitochondrion. 2019 Mar;45:1-6. doi: 10.1016/j.mito.2018.01.008. Epub 2018 Jan 31.

Core I gene is overexpressed in Hürthle and non-Hürthle cell microfollicular adenomas and follicular carcinomas of the thyroid.

BMC Cancer. 2004 Mar 25;4:12. doi: 10.1186/1471-2407-4-12.

Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors.

Proc Natl Acad Sci U S A. 2007 May 22;104(21):9001-6. doi: 10.1073/pnas.0703056104. Epub 2007 May 15.

[Analysis of mitochondrial DNA D-loop region mutation and its significance in human oncocytoma].

Zhonghua Zhong Liu Za Zhi. 2010 Oct;32(10):767-70.

引用本文的文献

Mitochondrial DNA disorders in neuromuscular diseases in diverse populations.

Ann Clin Transl Neurol. 2024 Aug 2. doi: 10.1002/acn3.52141.

Rare Diseases of the Orbit.

Laryngorhinootologie. 2021 Apr;100(S 01):S1-S79. doi: 10.1055/a-1384-4641. Epub 2021 Apr 30.

Mitochondrial DNA variation and cancer.

Nat Rev Cancer. 2021 Jul;21(7):431-445. doi: 10.1038/s41568-021-00358-w. Epub 2021 May 27.

Mitochondrial somatic mutations and the lack of viral genomic variation in recurrent respiratory papillomatosis.

Sci Rep. 2019 Nov 12;9(1):16625. doi: 10.1038/s41598-019-53148-8.

Oncogenes, mitochondrial metabolism, and quality control in differentiated thyroid cancer.

Korean J Intern Med. 2017 Sep;32(5):780-789. doi: 10.3904/kjim.2016.420. Epub 2017 Aug 22.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells.

Cancer Metab. 2013 Mar 18;1(1):11. doi: 10.1186/2049-3002-1-11.

Relevance of mitochondrial genetics and metabolism in cancer development.

Cold Spring Harb Perspect Biol. 2013 Feb 1;5(2):a011411. doi: 10.1101/cshperspect.a011411.

Mitochondria and cancer.

Nat Rev Cancer. 2012 Oct;12(10):685-98. doi: 10.1038/nrc3365.

HmtDB, a genomic resource for mitochondrion-based human variability studies.

Nucleic Acids Res. 2012 Jan;40(Database issue):D1150-9. doi: 10.1093/nar/gkr1086. Epub 2011 Dec 1.