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ArticlesPeer ReviewedFull Text
Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathy
Author / Creator:Masoumi, Tannaz ; Hesami, Hamed ; Maleki, Majid ; Kalayinia, Samira
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2025-04, Vol.18 (1), p.82-7, Article 82
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Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature
Author / Creator:Sorrentino, Ugo ; Gabbiato, Ilaria ; Canciani, Chiara ; Calosci, Davide ; Rigon, Chiara ; Zuccarello, Daniela ; Cassina, Matteo
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2023-03, Vol.14 (3), p.748
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Pediatric hypertrophic cardiomyopathy caused by a novel TNNI3 variant
Publisher:London: Springer Nature B.V
Journal title:Human genome variation, 2024-03, Vol.11 (1), p.14
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De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents
Author / Creator:Hassoun, Roua ; Budde, Heidi ; Mannherz, Hans Georg ; Lódi, Mária ; Fujita-Becker, Setsuko ; Laser, Kai Thorsten ; Gärtner, Anna ; Klingel, Karin ; Möhner, Desirée ; Stehle, Robert ; Sultana, Innas ; Schaaf, Thomas ; Majchrzak, Mario ; Krause, Verena ; Herrmann, Christian ; Nowaczyk, Marc M. ; Mügge, Andreas ; Pfitzer, Gabriele ; Schröder, Rasmus R. ; Hamdani, Nazha ; Milting, Hendrik ; Jaquet, Kornelia ; Cimiotti, Diana
Publisher:Basel: MDPI AG
Journal title:International journal of molecular sciences, 2021-09, Vol.22 (17), p.9625
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Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy
Author / Creator:Kraoua, Lilia ; Louati, Assaad ; Ahmed, Sarra Ben ; Abida, Nesrine ; Khemiri, Monia ; Menif, Khaled ; Mrad, Ridha ; Zaffran, Stéphane ; Jaouadi, Hager
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2024-06, Vol.12 (6), p.e2486-n/a
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Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants
Author / Creator:Janin, Alexandre ; Perouse de Montclos, Thomas ; Nguyen, Karine ; Consolino, Emilie ; Nadeau, Gwenael ; Rey, Gaelle ; Bouchot, Océane ; Blanchet, Patricia ; Sabbagh, Quentin ; Cazeneuve, Cécile ; El-Malti, Rajae ; Morel, Elodie ; Delinière, Antoine ; Chevalier, Philippe ; Millat, Gilles
Publisher:Cham: Springer International Publishing
Journal title:Molecular diagnosis & therapy, 2022-09, Vol.26 (5), p.551-560
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Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population
Author / Creator:Wang, Chuchu ; Wu, Manman ; Qian, Jin ; Li, Bin ; Tu, Xin ; Xu, Chengqi ; Li, Sisi ; Chen, Shanshan ; Zhao, Yuanyuan ; Huang, Yufeng ; Shi, Lisong ; Cheng, Xiang ; Liao, Yuhua ; Chen, Qiuyun ; Xia, Yunlong ; Yao, Wei ; Wu, Gang ; Cheng, Mian ; Wang, Qing K.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Molecular genetics and genomics : MGG, 2016-02, Vol.291 (1), p.79-92
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A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)
Author / Creator:Pantou, Malena P. ; Gourzi, Polyxeni ; Gkouziouta, Aggeliki ; Armenis, Iakovos ; Kaklamanis, Loukas ; Zygouri, Christianna ; Constantoulakis, Pantelis ; Adamopoulos, Stamatis ; Degiannis, Dimitrios
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genetics, 2019-04, Vol.20 (1), p.61-6, Article 61
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Circulating miR-1246 Targeting UBE2C, TNNI3, TRAIP, UCHL1 Genes and Key Pathways as a Potential Biomarker for Lung Adenocarcinoma: Integrated Biological Network Analysis
Author / Creator:Huang, Siyuan ; Wei, Yong-Kai ; Kaliamurthi, Satyavani ; Cao, Yanghui ; Nangraj, Asma Sindhoo ; Sui, Xin ; Chu, Dan ; Wang, Huan ; Wei, Dong-Qing ; Peslherbe, Gilles H. ; Selvaraj, Gurudeeban ; Shi, Jiang
Publisher:MDPI
Journal title:Journal of personalized medicine, 2020-10, Vol.10 (4), p.162
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High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians
Author / Creator:Rani, Deepa Selvi ; Nallari, Pratibha ; Priyamvada, Singh ; Narasimhan, Calambur ; Singh, Lalji ; Thangaraj, Kumarasamy
Publisher:England: BioMed Central
Journal title:BMC genetics, 2012-08, Vol.13 (1), p.69-69, Article 69
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Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy
Author / Creator:Mouton, JM ; Pellizzon, AS ; Goosen, A ; Kinnear, CJ ; Herbst, PG ; Brink, PA ; Moolman-Smook, JC
Publisher:Durbanville: Clinics Cardive Publishing
Journal title:Cardiovascular Journal Of Africa, 2015-03, Vol.26 (2), p.63-69
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Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier
Author / Creator:Yang, Shi Wei ; Hitz, Marc-Phillip ; Andelfinger, Gregor
Publisher:Cambridge, UK: Cambridge University Press
Journal title:Cardiology in the young, 2010-10, Vol.20 (5), p.574-576
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Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy : ca...
Author / Creator:Mouton, Jomien M. ; Moolman-Smook, Johanna C. ; Brink, Paul A ; Goosen, Althea ; Pellizzon, Adriano S. ; Herbst, Philip G. ; Kinnear, Craig J.
Publisher:Clinics Cardive Publishing
Journal title:Cardiovascular Journal of Africa, 2015-03, Vol.26 (2), p.63-69
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Pediatric restrictive cardiomyopathy: a case report
Author / Creator:Dai, Hai-Long ; Wang, Qing-Hui ; Su, Xuan ; Ding, Yun-Chuan ; Guang, Xue-Feng
Publisher:London, England: SAGE Publications
Journal title:Journal of international medical research, 2023-08, Vol.51 (8), p.3000605231188276
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Role of Whole-exome Sequencing in Phenotype Classification and Clinical Treatment of Pediatric Restrictive Cardiomyopathy
Author / Creator:Ding, Wen-Hong ; Han, Ling ; Xiao, Yan-Yan ; Mo, Ying ; Yang, Jing ; Wang, Xiao-Fang ; Jin, Mei
Publisher:China: Medknow Publications and Media Pvt. Ltd
Journal title:Chinese medical journal, 2017-12, Vol.130 (23), p.2823-2828
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Hearts of this ILK rely on TNNI3K, a MAPKKK that regulates TNNI3
Author / Creator:Luft, Friedrich C.
Publisher:Berlin: Springer
Journal title:Journal of molecular medicine (Berlin, Germany), 2003-05, Vol.81 (5), p.279-280
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Clinical genetic testing in four highly suspected pediatric restrictive cardiomyopathy cases
Author / Creator:Zheng, Min ; Huang, Hong ; Zhu, Xu ; Ho, Harvey ; Li, Liling ; Ji, Xiaojuan
Publisher:England: BioMed Central Ltd
Journal title:BMC cardiovascular disorders, 2022-05, Vol.22 (1), p.240-8, Article 240
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TNNI3 interacting kinase (TNNI3K)
Publisher:New York: Nature Publishing Group US
Journal title:SciBX, 2013-11, Vol.6 (44), p.1255-1255
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Hearts of this ILK rely on TNNI3K, a MAPKKK that regulated TNNI3
Author / Creator:Luft, Friedrich C
Publisher:Germany
Journal title:Journal of molecular medicine (Berlin, Germany), 2003-05, Vol.81 (5), p.279
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Data on Dilated Cardiomyopathy Detailed by a Researcher at University of Padova (Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature)
Publisher:NewsRX LLC
Journal title:Obesity, fitness, & wellness week, 2023-04, p.1490
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Exploring the c.406 C > T variant in TNNI3 gene: pathogenic insights into restrictive cardiomyopathy

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Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature

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Pediatric hypertrophic cardiomyopathy caused by a novel TNNI3 variant

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De Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents

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Homozygous TNNI3 frameshift variant in a consanguineous family with lethal infantile dilated cardiomyopathy

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Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants

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Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population

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A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)

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Circulating miR-1246 Targeting UBE2C, TNNI3, TRAIP, UCHL1 Genes and Key Pathways as a Potential Biomarker for Lung Adenocarcinoma: Integrated Biological Network Analysis

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High prevalence of Arginine to Glutamine Substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians

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Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy

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Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier

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Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy : ca...

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Pediatric restrictive cardiomyopathy: a case report

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Role of Whole-exome Sequencing in Phenotype Classification and Clinical Treatment of Pediatric Restrictive Cardiomyopathy

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Hearts of this ILK rely on TNNI3K, a MAPKKK that regulates TNNI3

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Clinical genetic testing in four highly suspected pediatric restrictive cardiomyopathy cases

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TNNI3 interacting kinase (TNNI3K)

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Hearts of this ILK rely on TNNI3K, a MAPKKK that regulated TNNI3

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Data on Dilated Cardiomyopathy Detailed by a Researcher at University of Padova (Homozygous TNNI3 Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the Literature)

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