Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy

Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Carballo, S, Blair, E, Watkins, H
التنسيق:	Conference item
منشور في:	2005

مواد مشابهة

Novel mutations in cardiac MYBPC3 and early onset malignant hypertrophic cardiomyopathy
حسب: Carballo, S, وآخرون
منشور في: (2005)

Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
حسب: Carballo, S, وآخرون
منشور في: (2003)

Novel mutations in cardiac MYPBC3 cause early onset malignant hypertrophic cardiomyopathy (HCM)
حسب: Carballo, S, وآخرون
منشور في: (2005)

How do MYBPC3 mutations cause hypertrophic cardiomyopathy?
حسب: Marston, S, وآخرون
منشور في: (2012)

Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin
حسب: Toepfer, C, وآخرون
منشور في: (2019)

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency.
حسب: Marston, S, وآخرون
منشور في: (2009)

Autosomal recessive transmission of MYBPC3 mutation results in malignant phenotype of hypertrophic cardiomyopathy.
حسب: Yilu Wang, وآخرون
منشور في: (2013-01-01)

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the <it>MYBPC3 </it>gene
حسب: Lehrke Stephanie, وآخرون
منشور في: (2008-10-01)

A novel Loss-of-function Mutation in MYBPC3 Causes familial hypertrophic cardiomyopathy with extreme intrafamilial phenotypic heterogeneity
حسب: Peng Y, وآخرون
منشور في: (2023-03-01)

A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
حسب: Carballo, S, وآخرون
منشور في: (2004)

Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene
حسب: Olgu Hallioglu Kilinc, وآخرون
منشور في: (2017-07-01)

The Metabolome in Finnish Carriers of the MYBPC3-Q1061X Mutation for Hypertrophic Cardiomyopathy.
حسب: Benedicte Jørgenrud, وآخرون
منشور في: (2015-01-01)

Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients
حسب: Behnaz Sadat Abedi, وآخرون
منشور في: (2015-08-01)

Novel MYBPC3 Mutations in Indian Population with Cardiomyopathies
حسب: Rani DS, وآخرون
منشور في: (2023-09-01)

MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy.
حسب: James W McNamara, وآخرون
منشور في: (2017-01-01)

Hypertrophic cardiomyopathy in myosin-binding protein C (MYBPC3) Icelandic founder mutation carriers
حسب: Javier Diez, وآخرون
منشور في: (2020-06-01)

A pathogenic nonsense mutation (c.1522C>T) of the MYBPC3 gene is implicated with hypertrophic cardiomyopathy
حسب: Erru Ni, وآخرون
منشور في: (2023-08-01)

A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy
حسب: Harper, AR, وآخرون
منشور في: (2020)

Transcriptome Analysis of Cardiac Hypertrophic Growth in MYBPC3-Null Mice Suggests Early Responders in Hypertrophic Remodeling
حسب: Emily Farrell, وآخرون
منشور في: (2018-10-01)

Pathogenic intronic splice-affecting variants in MYBPC3 in three patients with hypertrophic cardiomyopathy
حسب: Wood, KA, وآخرون
منشور في: (2021)

Epigenetic Study of Cohort of Monozygotic Twins With Hypertrophic Cardiomyopathy Due to MYBPC3 (Cardiac Myosin‐Binding Protein C)
حسب: Alfonso Peñarroya, وآخرون
منشور في: (2024-11-01)

Autosomal dominant familial dilated cardiomyopathy caused by a novel mutation in phospholamban
حسب: Carballo, S, وآخرون
منشور في: (2004)

MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations
حسب: Li-rong Lin, وآخرون
منشور في: (2022-06-01)

Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree
حسب: Mario Torrado, وآخرون
منشور في: (2022-05-01)

Myocardial dysfunction caused by MyBPC3 P459fs mutation in hypertrophic cardiomyopathy: evidence from multi-omics approaches and super-resolution imaging
حسب: Yupeng Wu, وآخرون
منشور في: (2025-02-01)

Pathogenic Intronic Splice-Affecting Variants in <i>MYBPC3</i> in Three Patients with Hypertrophic Cardiomyopathy
حسب: Katherine A. Wood, وآخرون
منشور في: (2021-06-01)

MYBPC3Δ25bp intronic deletion in hypertrophic cardiomyopathy patients and healthy Iranian population
حسب: Leila Emrahi, وآخرون
منشور في: (2021-04-01)

Repair of Mybpc3 mRNA by 5′-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy
حسب: Giulia Mearini, وآخرون
منشور في: (2013-01-01)

A human <it>MYBPC3</it> mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death
حسب: Teirlinck Carolien H, وآخرون
منشور في: (2012-11-01)

Western diet triggers cardiac dysfunction in heterozygous Mybpc3-targeted knock-in mice: A two-hit model of hypertrophic cardiomyopathy
حسب: Edgar E. Nollet, وآخرون
منشور في: (2023-12-01)

Erratum: How do MYBPC3 mutations cause hypertrophic cardiomyopathy? (Journal of Muscle Research and Cell Motility DOI 10.1007/s10974-011-9268-3)
حسب: Marston, S, وآخرون
منشور في: (2012)

Inhibition of HSC70 alleviates hypertrophic cardiomyopathy pathology in human induced pluripotent stem cell‐derived cardiomyocytes with a MYBPC3 mutation
حسب: Hangyuan Qiu, وآخرون
منشور في: (2021-12-01)

Generation of induced pluripotent stem cell lines from two unrelated individuals with familial hypertrophic cardiomyopathy carrying MYBPC3 nonsense mutations
حسب: Marta Ribeiro, وآخرون
منشور في: (2024-04-01)

Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
حسب: Abdulrazzak, H, وآخرون
منشور في: (2001)

AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy models
حسب: Amara Greer-Short, وآخرون
منشور في: (2025-03-01)

Metabolic remodeling and calcium handling abnormality in induced pluripotent stem cell-derived cardiomyocytes in dilated phase of hypertrophic cardiomyopathy with MYBPC3 frameshift mutation
حسب: Haruka Mori, وآخرون
منشور في: (2024-07-01)

Presence of known feline ALMS1 and MYBPC3 variants in a diverse cohort of cats with hypertrophic cardiomyopathy in Japan.
حسب: Noriyoshi Akiyama, وآخرون
منشور في: (2023-01-01)

Generation of two iPSC lines from hypertrophic cardiomyopathy patients carrying MYBPC3 and PRKAG2 variants
حسب: Amit Manhas, وآخرون
منشور في: (2022-05-01)

Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
حسب: Burton, D, وآخرون
منشور في: (2002)

Two mutations in human cardiac troponin I known to cause hypertrophic cardiomyopathy have different effects on cardiac muscle contraction
حسب: Burton, D, وآخرون
منشور في: (2000)