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Detection of heterozygous c.1708C>T and c.1978C>G thyroid peroxidase (TPO) mutations in Iraqi patients with toxic and nontoxic goiter

https://doi.org/10.1007/s00580-012-1572-9
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archinte.148.3.626openalex-snapshot
Graves' disease. Influence of age on clinical findings
inferredcites →https://doi.org/10.1001/archinte.1988.00380030132023openalex-snapshot
Graves' Disease
inferredcites →https://doi.org/10.1002/humu.1380060104openalex-snapshot
Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis
inferredcites →https://doi.org/10.1007/s00251-002-0453-9openalex-snapshot
The human anti-thyroid peroxidase autoantibody repertoire in Graves' and Hashimoto's autoimmune thyroid diseases
inferredcites →https://doi.org/10.1007/s12020-009-9280-1openalex-snapshot
Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/0888-7543(95)80028-kopenalex-snapshot
Regional localization of the gene for thyroid peroxidase to human chromosome 2p25 and mouse chromosome 12C
inferredcites →https://doi.org/10.1016/s0040-4020(98)00094-5openalex-snapshot
LNA (Locked Nucleic Acids): Synthesis of the adenine, cytosine, guanine, 5-methylcytosine, thymine and uracil bicyclonucleoside monomers, oligomerisation, and unprecedented nucleic acid recognition
inferredcites →https://doi.org/10.1016/s0040-4039(98)01084-3openalex-snapshot
Stability and structural features of the duplexes containing nucleoside analogues with a fixed N-type conformation, 2′-O,4′-C-methyleneribonucleosides
inferredcites →https://doi.org/10.1016/s0304-3835(00)00697-2openalex-snapshot
Thyroid cancer
inferredcites →https://doi.org/10.1038/ng1297-411openalex-snapshot
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
inferredcites →https://doi.org/10.1039/a708608copenalex-snapshot
LNA (locked nucleic acids): synthesis and high-affinity nucleic acid recognition
inferredcites →https://doi.org/10.1046/j.1365-2265.1999.00746.xopenalex-snapshot
A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect
inferredcites →https://doi.org/10.1046/j.1365-2265.2003.01823.xopenalex-snapshot
Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings
inferredcites →https://doi.org/10.1056/nejmoa012752openalex-snapshot
Inactivating Mutations in the Gene for Thyroid Oxidase 2 (THOX2) and Congenital Hypothyroidism
inferredcites →https://doi.org/10.1081/hem-100105221openalex-snapshot
THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION
inferredcites →https://doi.org/10.1089/105072501750362763openalex-snapshot
Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene
inferredcites →https://doi.org/10.1093/nar/29.1.17openalex-snapshot
The EMBL nucleotide sequence database
inferredcites →https://doi.org/10.1093/nar/29.17.e88openalex-snapshot
An efficient procedure for genotyping single nucleotide polymorphisms
inferredcites →https://doi.org/10.1093/nar/gki033openalex-snapshot
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
inferredcites →https://doi.org/10.1097/00000441-195610000-00020openalex-snapshot
THE THYROID. A FUNDAMENTAL AND CLINICAL TEXT
inferredcites →https://doi.org/10.1097/00008480-200108000-00014openalex-snapshot
Genetic defects in thyroid hormone synthesis
inferredcites →https://doi.org/10.1097/med.0b013e32832ff218openalex-snapshot
Mutations of the thyroglobulin gene and its relevance to thyroid disorders
inferredcites →https://doi.org/10.1111/j.1365-2265.2007.02804.xopenalex-snapshot
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in Israelis
inferredcites →https://doi.org/10.1136/jmg.2004.024158openalex-snapshot
Genetics of congenital hypothyroidism
inferredcites →https://doi.org/10.1148/radiology.173.2.2678263openalex-snapshot
Thyroid gland: US screening in middle-aged women with no previous thyroid disease.
inferredcites →https://doi.org/10.1148/radiology.215.3.r00jn07801openalex-snapshot
Importance of Thyroid Abnormalities Detected at US Screening: A 5-year Follow-up
inferredcites →https://doi.org/10.1155/2010/351679openalex-snapshot
Thyroid Cancer: Current Molecular Perspectives
inferredcites →https://doi.org/10.1172/jci115981openalex-snapshot
Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.
inferredcites →https://doi.org/10.1210/edrv-14-2-165openalex-snapshot
Defective Thyroglobulin Synthesis and Secretion Causing Goiter and Hypothyroidism *
inferredcites →https://doi.org/10.1210/jc.2002-020153openalex-snapshot
High Prevalence of a Novel Mutation (2268 insT) of the Thyroid Peroxidase Gene in Taiwanese Patients with Total Iodide Organification Defect, and Evidence for a Founder Effect
inferredcites →https://doi.org/10.1210/jc.2005-2302openalex-snapshot
Metastatic Follicular Thyroid Carcinoma Arising from Congenital Goiter as a Result of a Novel Splice Donor Site Mutation in the Thyroglobulin Gene
inferredcites →https://doi.org/10.1210/jc.2006-1242openalex-snapshot
Thyroglobulin Gene Mutations Producing Defective Intracellular Transport of Thyroglobulin Are Associated with Increased Thyroidal Type 2 Iodothyronine Deiodinase Activity
inferredcites →https://doi.org/10.1210/jc.2006-1402openalex-snapshot
Influences of Age, Gender, Smoking, and Family History on Autoimmune Thyroid Disease Phenotype
inferredcites →https://doi.org/10.1210/jc.2007-2276openalex-snapshot
Pseudodominant Inheritance of Goitrous Congenital Hypothyroidism Caused by TPO Mutations: Molecular and in Silico Studies
inferredcites →https://doi.org/10.1210/jc.2010-2583openalex-snapshot
Approach to the Patient with Nontoxic Multinodular Goiter
inferredcites →https://doi.org/10.1210/jc.77.1.210openalex-snapshot
A nonsense mutation causes human hereditary congenital goiter with preferential production of a 171-nucleotide-deleted thyroglobulin ribonucleic acid messenger
inferredcites →https://doi.org/10.1210/jcem-72-2-471openalex-snapshot
Genetic Linkage Studies of Thyroid Peroxidase (TPO) Gene in Families with TPO Deficiency*
inferredcites →https://doi.org/10.1210/jcem.79.1.8027236openalex-snapshot
A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism
inferredcites →https://doi.org/10.1210/jcem.82.2.3729openalex-snapshot
Molecular Analysis of Mutated Thyroid Peroxidase Detected in Patients with Total Iodide Organification Defects1
inferredcites →https://doi.org/10.1210/jcem.84.3.5541openalex-snapshot
Two Different Mutations in the Thyroid Peroxidase Gene of a Large Inbred Amish Kindred: Power and Limits of Homozygosity Mapping1
inferredcites →https://doi.org/10.1210/jcem.85.10.6878openalex-snapshot
Two Decades of Screening for Congenital Hypothyroidism in the Netherlands: TPO Gene Mutations in Total Iodide Organification Defects (an Update)
inferredcites →https://doi.org/10.1210/jcem.86.3.7313openalex-snapshot
Maternal Isodisomy for Chromosome 2p Causing Severe Congenital Hypothyroidism
inferredcites →https://doi.org/10.1210/jcem.87.5.8504openalex-snapshot
Risk of Malignancy in Nonpalpable Thyroid Nodules: Predictive Value of Ultrasound and Color-Doppler Features
inferredcites →https://doi.org/10.1385/0-89603-346-5:169openalex-snapshot
Hemoglobinopathies: Community Clues to Mutation Detection
inferredcites →https://doi.org/10.1530/eje-07-0037openalex-snapshot
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis
inferredcites →https://doi.org/10.1530/eje.0.1450019openalex-snapshot
Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism
inferredcites →https://doi.org/10.1530/eje.0.1460491openalex-snapshot
Two novel missense mutations in the thyroid peroxidase gene, R665W and G771R, result in a localization defect and cause congenital hypothyroidism
inferredcites →https://doi.org/10.1677/joe.0.1600267openalex-snapshot
A novel mutation in the human thyroid peroxidase gene resulting in a total iodide organification defect
inferredcites →https://doi.org/10.1677/joe.0.1720627openalex-snapshot
Mutation analysis of thyroid peroxidase gene in Chinese patients with total iodide organification defect: identification of five novel mutations
inferredcites →https://doi.org/10.2337/diab.20.12.839bopenalex-snapshot
The Thyroid: A Fundamental and Clinical Text
inferredcites →https://doi.org/10.4061/2011/264248openalex-snapshot
Predominant RET Germline Mutations in Exons 10, 11, and 16 in Iranian Patients with Hereditary Medullary Thyroid Carcinoma

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4145417openalex-extracted
inferred← citeshttps://doi.org/10.1007/s00580-012-1671-7openalex-snapshot
Micronucleus frequency among Iraqi thyroid disorder patients
inferred← citeshttps://doi.org/10.1007/s12020-022-03054-3openalex-snapshot
Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis
inferred← citeshttps://doi.org/10.1016/j.mce.2022.111748openalex-snapshot
Curating the GnomAD Database: Report of Novel Variants in the Thyroid Peroxidase Gene Using In Silico Bioinformatics Algorithms and a Literature Review
inferred← citeshttps://doi.org/10.1038/s41587-021-00943-2openalex-snapshot
Adenine base editor engineering reduces editing of bystander cytosines
inferred← citeshttps://doi.org/10.1134/s0006297925604265openalex-snapshot
Thyroid Peroxidase Gene Mutations Associated with Thyroid Disorders
inferred← citeshttps://doi.org/10.2478/folmed-2018-0078openalex-snapshot
Genetics of Thyroid Disorders
inferred← citeshttps://doi.org/10.3923/jms.2013.676.683openalex-snapshot
Detection of T.G. and TO Genes Compound Mutations Associated with Thyroid Carcinoma, Toxic Goiter and Hypothyroidism in Iraqi Patients
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