Commentary on "Deciphering the mystery of CHNG3".
作者信息
Cheon Chong Kun
机构信息
Department of Pediatrics, Pusan National University Children's Hospital, Yangsan, Korea.
出版信息
Ann Pediatr Endocrinol Metab. 2024 Oct;29(5):277-278. doi: 10.6065/apem.2424093edi05. Epub 2024 Oct 31.
Abstract
摘要
相似文献
1
Commentary on "Deciphering the mystery of CHNG3".关于《解读CHNG3之谜》的评论
Ann Pediatr Endocrinol Metab. 2024 Oct;29(5):277-278. doi: 10.6065/apem.2424093edi05. Epub 2024 Oct 31.
2
Deciphering the mystery of CHNG3.破解CHNG3的奥秘。
Ann Pediatr Endocrinol Metab. 2024 Oct;29(5):279-283. doi: 10.6065/apem.2448186.093. Epub 2024 Oct 31.
3
Deciphering the mystery of the leaky pulmonary valve in a new era of interventional cardiology.在介入心脏病学的新时代破解肺动脉瓣反流之谜。
Eur Heart J. 2007 Aug;28(15):1793-4. doi: 10.1093/eurheartj/ehm261. Epub 2007 Jun 26.
4
No easy way to explain cosmic expansion mystery.解释宇宙膨胀之谜没有简单的方法。
Science. 2023 Nov 3;382(6670):499-500. doi: 10.1126/science.adm6799. Epub 2023 Nov 2.
5
Deciphering the mystery of hexagon holes in an all-boron graphene α-sheet.解读全硼石墨烯 α 片层中六方孔的奥秘。
Phys Chem Chem Phys. 2011 Jun 28;13(24):11575-8. doi: 10.1039/c1cp20439d. Epub 2011 May 20.
6
Deciphering the mystery of combined factor V and factor VIII deficiency.破解联合因子V和因子VIII缺乏症之谜。
J Thromb Haemost. 2006 May;4(5):927-31. doi: 10.1111/j.1538-7836.2006.01939.x.
7
Deciphering the Mystery: Extracorporeal Photopheresis in Graft-versus-Host Disease.揭开谜团：体外光化学疗法治疗移植物抗宿主病
Biol Blood Marrow Transplant. 2015 Nov;21(11):1861-2. doi: 10.1016/j.bbmt.2015.09.011. Epub 2015 Sep 18.
8
Commentary: Bleeding events with novel bioprostheses: Still a mystery.评论：新型生物假体的出血事件：仍是一个谜。
J Thorac Cardiovasc Surg. 2021 Jan;161(1):78-79. doi: 10.1016/j.jtcvs.2019.10.052. Epub 2019 Oct 24.
9
Commentary: A riddle wrapped in a mystery inside an enigma.评论：一个包裹在谜团之中、深藏于奥秘之内的谜题。
J Thorac Cardiovasc Surg. 2022 Dec;164(6):1818-1819. doi: 10.1016/j.jtcvs.2021.01.041. Epub 2021 Jan 20.
10
Commentary: The immunologic mystery of cardiac myxoma.评论：心脏黏液瘤的免疫学之谜。
JTCVS Tech. 2020 Jan 10;1:73-74. doi: 10.1016/j.xjtc.2020.01.012. eCollection 2020 Mar.
本文引用的文献
1
Deciphering the mystery of CHNG3.破解CHNG3的奥秘。
Ann Pediatr Endocrinol Metab. 2024 Oct;29(5):279-283. doi: 10.6065/apem.2448186.093. Epub 2024 Oct 31.
2
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.15q26.1 上的 TTTG 微卫星中的功能变体导致家族性非自身免疫性甲状腺异常。
Nat Genet. 2024 May;56(5):869-876. doi: 10.1038/s41588-024-01735-5. Epub 2024 May 7.
3
Genetics of congenital hypothyroidism: Modern concepts.先天性甲状腺功能减退症的遗传学：现代概念
Pediatr Investig. 2022 May 14;6(2):123-134. doi: 10.1002/ped4.12324. eCollection 2022 Jun.
4
Genome wide characterization of simple sequence repeats in watermelon genome and their application in comparative mapping and genetic diversity analysis.西瓜基因组中简单序列重复序列的全基因组特征分析及其在比较作图和遗传多样性分析中的应用。
BMC Genomics. 2016 Aug 5;17:557. doi: 10.1186/s12864-016-2870-4.
5
Clinical description of infants with congenital hypothyroidism and iodide organification defects.先天性甲状腺功能减退症合并碘有机化缺陷婴儿的临床描述。
Horm Res. 2008;70(4):240-8. doi: 10.1159/000151597. Epub 2008 Sep 5.
6
Microsatellites: simple sequences with complex evolution.微卫星：具有复杂进化的简单序列。
Nat Rev Genet. 2004 Jun;5(6):435-45. doi: 10.1038/nrg1348.
7
Microsatellites in different eukaryotic genomes: survey and analysis.不同真核生物基因组中的微卫星：调查与分析。
Genome Res. 2000 Jul;10(7):967-81. doi: 10.1101/gr.10.7.967.
Zotero 插件