Search Results - "Burczyk MS"

Transcriptome profile of the sinoatrial ring reveals conserved and novel genetic programs of the zebrafish pacemaker.

Authors: Minhas, Rashid Loeffler-Wirth, Henry Siddiqui, Yusra H. et al.

Source: BMC Genomics. 10/2/2021, Vol. 22 Issue 1, p1-15. 15p.

Semaphorin3f as a cardiomyocyte derived regulator of heart chamber development.

Authors: Halabi, Rami Cechmanek, Paula Bernice Hehr, Carrie Lynn et al.

Source: Cell Communication & Signaling. 8/19/2022, Vol. 20 Issue 1, p1-23. 23p.

Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies.

Authors: Wang, E Fan, X Nie, Y et al.

Source: Balkan Journal of Medical Genetics. 2021, Vol. 24 Issue 2, p39-47. 9p.

Zebrafish in Cardiovascular Disease Research: from Model to Application.

Authors: Wang R Zhang Q Zhang S et al.

Source: International journal of biological sciences [Int J Biol Sci] 2026 Apr 23; Vol. 22 (9), pp. 4806-4825. Date of Electronic Publication: 2026 Apr 23 (Print Publication: 2026).

Publication Type: Journal Article; Review

Journal Info: Publisher: Ivyspring International Country of Publication: Australia NLM ID: 101235568 Publication Model: eCollection Cited Medium: Internet ISSN: 1449-2288 (Electronic) Linking ISSN: 14492288 NLM ISO Abbreviation: Int J Biol Sci Subsets: MEDLINE

Broadening horizons: new links between cilia and heart development and disease.

Authors: Ma W Zhang Z Ma Y et al.

Source: Frontiers in cardiovascular medicine [Front Cardiovasc Med] 2026 Feb 17; Vol. 13, pp. 1699088. Date of Electronic Publication: 2026 Feb 17 (Print Publication: 2026).

Publication Type: Journal Article; Review

Journal Info: Publisher: Frontiers Media S.A Country of Publication: Switzerland NLM ID: 101653388 Publication Model: eCollection Cited Medium: Print ISSN: 2297-055X (Print) Linking ISSN: 2297055X NLM ISO Abbreviation: Front Cardiovasc Med Subsets: PubMed not MEDLINE

Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis.

Authors: Burkhalter MD Sridhar A Sampaio P et al.

Corporate Authors: Burkhalter MD Sridhar A Sampaio P et al.

Source: The Journal of clinical investigation [J Clin Invest] 2019 May 16; Vol. 129 (7), pp. 2841-2855. Date of Electronic Publication: 2019 May 16.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model: Electronic Cited Medium: Internet ISSN: 1558-8238 (Electronic) Linking ISSN: 00219738 NLM ISO Abbreviation: J Clin Invest Subsets: MEDLINE

Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies.

Authors: Hempel M Casar Tena T Diehl T et al.

Source: Human genetics [Hum Genet] 2017 Mar; Vol. 136 (3), pp. 339-346. Date of Electronic Publication: 2017 Feb 08.

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

TAp73 regulates mitochondrial dynamics and multiciliated cell homeostasis through an OPA1 axis.

Authors: Buckley NA Craxton A Sun XM et al.

Source: Cell death & disease [Cell Death Dis] 2024 Nov 08; Vol. 15 (11), pp. 807. Date of Electronic Publication: 2024 Nov 08.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101524092 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-4889 (Electronic) NLM ISO Abbreviation: Cell Death Dis Subsets: MEDLINE

Pathophysiology and pharmacology of G protein-coupled receptors in the heart.

Authors: Grogan A Lucero EY Jiang H et al.

Source: Cardiovascular research [Cardiovasc Res] 2023 May 22; Vol. 119 (5), pp. 1117-1129.

Publication Type: Review; Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: Oxford Journals Country of Publication: England NLM ID: 0077427 Publication Model: Print Cited Medium: Internet ISSN: 1755-3245 (Electronic) Linking ISSN: 00086363 NLM ISO Abbreviation: Cardiovasc Res Subsets: MEDLINE

Mitochondrial impairment and intracellular reactive oxygen species alter primary cilia morphology.

Authors: Moruzzi N Valladolid-Acebes I Kannabiran SA et al.

Source: Life science alliance [Life Sci Alliance] 2022 Sep 14; Vol. 5 (12). Date of Electronic Publication: 2022 Sep 14.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Life Science Alliance, LLC Country of Publication: United States NLM ID: 101728869 Publication Model: Electronic Cited Medium: Internet ISSN: 2575-1077 (Electronic) Linking ISSN: 25751077 NLM ISO Abbreviation: Life Sci Alliance Subsets: MEDLINE

Dnah9 mutant mice and organoid models recapitulate the clinical features of patients with PCD and provide an excellent platform for drug screening.

Authors: Zheng R Yang W Wen Y et al.

Source: Cell death & disease [Cell Death Dis] 2022 Jun 21; Vol. 13 (6), pp. 559. Date of Electronic Publication: 2022 Jun 21.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101524092 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-4889 (Electronic) NLM ISO Abbreviation: Cell Death Dis Subsets: MEDLINE

ISL1 loss-of-function mutation contributes to congenital heart defects.

Authors: Ma L Wang J Li L et al.

Source: Heart and vessels [Heart Vessels] 2019 Apr; Vol. 34 (4), pp. 658-668. Date of Electronic Publication: 2018 Nov 02.

Publication Type: Journal Article

Journal Info: Publisher: Springer Verlag Country of Publication: Japan NLM ID: 8511258 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1615-2573 (Electronic) Linking ISSN: 09108327 NLM ISO Abbreviation: Heart Vessels Subsets: MEDLINE

NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve.

Authors: Wang J Abhinav P Xu YJ et al.

Source: International journal of molecular medicine [Int J Mol Med] 2019 Apr; Vol. 43 (4), pp. 1839-1846. Date of Electronic Publication: 2019 Jan 31.

Publication Type: Journal Article

Journal Info: Publisher: D.A. Spandidos Country of Publication: Greece NLM ID: 9810955 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1791-244X (Electronic) Linking ISSN: 11073756 NLM ISO Abbreviation: Int J Mol Med