Search Results - "Salunga HT"

Bioinformatics and In-Silico Findings Reveal Candidate Genes for Tetralogy of Fallot via Integrative Multi-Omics Data.

Authors: Shi, Jiawei Wang, Zhen Bai, Ying et al.

Source: Congenital Heart Disease. 2025, Vol. 20 Issue 2, p213-229. 17p.

Specific induction of right ventricular-like cardiomyocytes from human pluripotent stem cells.

Authors: Saito, Yukihiro Nakamura, Kazufumi Katanosaka, Yuki et al.

Source: Stem Cell Research & Therapy. 9/26/2025, Vol. 16 Issue 1, p1-20. 20p.

Cardiac-specific overexpression of PRMT5 exacerbates pressure overload-induced hypertrophy and heart failure.

Authors: Katanasaka, Yasufumi Sunagawa, Yoichi Sakurai, Ryoga et al.

Source: Journal of Biomedical Science. 7/6/2025, Vol. 32 Issue 1, p1-17. 17p.

Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathy.

Authors: Kim, Oc-Hee Kim, Jihyun Kim, Youngjun et al.

Source: BMC Medical Genomics. 9/5/2024, Vol. 17 Issue 1, p1-12. 12p.

Cardiometabolic heart failure with preserved ejection fraction: from molecular signatures to personalized treatment.

Authors: Gorica, Era Geiger, Martin A. Di Venanzio, Ludovica et al.

Source: Cardiovascular Diabetology. 7/3/2025, Vol. 24 Issue 1, p1-17. 17p.

Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves.

Authors: Queen, Rachel Crosier, Moira Eley, Lorraine et al.

Source: PLoS Genetics. 11/27/2023, Vol. 19 Issue 11, p1-30. 30p.

Single-cell omics uncovers novel pathological mechanisms and therapeutic targets for congenital heart diseases: insights from integrated intercellular communication analysis.

Authors: Nguyen PT Sahara M

Source: Stem cell research & therapy [Stem Cell Res Ther] 2026 Apr 16; Vol. 17 (1). Date of Electronic Publication: 2026 Apr 16.

Publication Type: Journal Article; Review

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101527581 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-6512 (Electronic) Linking ISSN: 17576512 NLM ISO Abbreviation: Stem Cell Res Ther Subsets: MEDLINE

BET inhibitors in cardiovascular diseases: from atherosclerosis to heart failure.

Authors: Ala M Mohammad Khawajah I Shamshiri Khamene S

Source: Pharmacological reports : PR [Pharmacol Rep] 2026 Apr; Vol. 78 (2), pp. 405-422. Date of Electronic Publication: 2026 Jan 05.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer International Publishing Country of Publication: Switzerland NLM ID: 101234999 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2299-5684 (Electronic) Linking ISSN: 17341140 NLM ISO Abbreviation: Pharmacol Rep Subsets: MEDLINE

Co-occurrence of rare variants implicates gene pairs in cytoskeletal pathways and is associated with increased severity in autism spectrum disorder.

Authors: Lee H Ko K Kim S et al.

Source: Genome biology [Genome Biol] 2026 Mar 23; Vol. 27 (1). Date of Electronic Publication: 2026 Mar 23.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 100960660 Publication Model: Electronic Cited Medium: Internet ISSN: 1474-760X (Electronic) Linking ISSN: 14747596 NLM ISO Abbreviation: Genome Biol Subsets: MEDLINE

Next-generation molecular imaging of cardiac fibrosis.

Authors: Ezeani M Dweck MR Craig NJ

Source: The international journal of cardiovascular imaging [Int J Cardiovasc Imaging] 2026 Mar 21. Date of Electronic Publication: 2026 Mar 21.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer Country of Publication: United States NLM ID: 100969716 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1875-8312 (Electronic) Linking ISSN: 15695794 NLM ISO Abbreviation: Int J Cardiovasc Imaging Subsets: MEDLINE

Analysis of structural variation among inbred mouse strains.

Authors: Arslan, Ahmed Fang, Zhuoqing Wang, Meiyue et al.

Source: BMC Genomics. 3/2/2023, Vol. 24 Issue 1, p1-14. 14p.

ENU-based dominant genetic screen identifies contractile and neuronal gene mutations in congenital heart disease.

Authors: Luo, Xiaoxi Liu, Lifeng Rong, Haowei et al.

Source: Genome Medicine. 8/12/2024, Vol. 16 Issue 1, p1-16. 16p.

Current advances in human-induced pluripotent stem cell-based models and therapeutic approaches for congenital heart disease.

Authors: Cao M Liu Y Sun Y et al.

Source: Molecular and cellular biochemistry [Mol Cell Biochem] 2025 Jan; Vol. 480 (1), pp. 159-172. Date of Electronic Publication: 2024 Apr 18.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer Country of Publication: Netherlands NLM ID: 0364456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-4919 (Electronic) Linking ISSN: 03008177 NLM ISO Abbreviation: Mol Cell Biochem Subsets: MEDLINE

Mechanisms of myocardial reverse remodelling and its clinical significance: A scientific statement of the ESC Working Group on Myocardial Function.

Authors: Falcão‐Pires, Inês Ferreira, Ana Filipa Trindade, Fábio et al.

Source: European Journal of Heart Failure. Jul2024, Vol. 26 Issue 7, p1454-1479. 26p.

Investigation of the impact of bromodomain inhibition on cytoskeleton stability and contraction.

Authors: Bigger-Allen, Alexander Gheinani, Ali Hashemi Adam, Rosalyn M.

Source: Cell Communication & Signaling. 3/16/2024, Vol. 22 Issue 1, p1-19. 19p.

HAND factors regulate cardiac lineage commitment and differentiation from human pluripotent stem cells.

Authors: Guo, Huixin Hang, Chengwen Lin, Bowen et al.

Source: Stem Cell Research & Therapy. 2/5/2024, Vol. 15 Issue 1, p1-22. 22p.

Application of CRISPR-Cas9 gene editing for congenital heart disease.

Authors: Heeyoung Seok Rui Deng Cowan, Douglas B. et al.

Source: Clinical & Experimental Pediatrics. Jun2021, Vol. 64 Issue 6, p269-279. 11p.

Apabetalone and hospitalization for heart failure in patients following an acute coronary syndrome: a prespecified analysis of the BETonMACE study.

Authors: Nicholls, Stephen J. Schwartz, Gregory G. Buhr, Kevin A. et al.

Source: Cardiovascular Diabetology. 1/7/2021, Vol. 20 Issue 1, p1-9. 9p.

The benign nature and rare occurrence of cardiac myxoma as a possible consequence of the limited cardiac proliferative/ regenerative potential: a systematic review.

Authors: Shafi, Ovais Siddiqui, Ghazia Jaffry, Hassam A.

Source: BMC Cancer. 12/18/2023, Vol. 23 Issue 1, p1-46. 46p.

Unmasking Retinitis Pigmentosa complex cases by a whole genome sequencing algorithm based on open-access tools: hidden recessive inheritance and potential oligogenic variants.

Authors: González-del Pozo, María Fernández-Suárez, Elena Martín-Sánchez, Marta et al.

Source: Journal of Translational Medicine. 2/12/2020, Vol. 18 Issue 1, p1-12. 12p.