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Quoted phrase not found in phrase index: "Sick sinus syndrome 3, susceptibility to"
Page 1
Genetic predictors of sick sinus syndrome.
Timasheva Y, Badykov M, Akhmadishina L, Nasibullin T, Badykova E, Pushkareva A, Plechev V, Sagitov I, Zagidullin N. Timasheva Y, et al. Mol Biol Rep. 2021 Jun;48(6):5355-5362. doi: 10.1007/s11033-021-06517-4. Epub 2021 Jun 30. Mol Biol Rep. 2021. PMID: 34195885
Sick sinus syndrome (SSS) encompasses a group of conduction disorders characterized by the inability of sinoatrial node to perform its pacemaker function. Our aim was to identify genetic predictors of SSS in a prospective cohort of patients admitted to …
Sick sinus syndrome (SSS) encompasses a group of conduction disorders characterized by the inability of sinoatrial node …
First Case of Invasive Stachybotrys Sinusitis.
Semis M, Dadwal SS, Tegtmeier BR, Wilczynski SP, Ito JI, Kalkum M. Semis M, et al. Clin Infect Dis. 2021 Apr 26;72(8):1386-1391. doi: 10.1093/cid/ciaa231. Clin Infect Dis. 2021. PMID: 32155243
BACKGROUND: The toxigenic mold Stachybotrys has controversially been linked to idiopathic pulmonary hemorrhage and "sick building syndrome." However, there are no previous clinical records of invasive stachybotryosis. ...RESULTS: Hemorrhage, fungal germination, and …
BACKGROUND: The toxigenic mold Stachybotrys has controversially been linked to idiopathic pulmonary hemorrhage and "sick building …
Evidence for reduced susceptibility to cardiac bradycardias in South Asians compared with Caucasians.
Yuyun MF, Squire IB, Ng GA, Samani NJ. Yuyun MF, et al. Heart. 2018 Aug;104(16):1350-1355. doi: 10.1136/heartjnl-2017-312374. Epub 2018 Feb 20. Heart. 2018. PMID: 29463611
OBJECTIVES: To investigate ethnic differences in susceptibility to bradycardias in South Asian and white European patients in the UK by determining rates of permanent pacemaker (PPM) implantation for sinus node dysfunction (SND) and atrioventricular block (AVB) in e …
OBJECTIVES: To investigate ethnic differences in susceptibility to bradycardias in South Asian and white European patients in the UK …
Genetic mutation of familial dilated cardiomyopathy based on next‑generation semiconductor sequencing.
Lin XF, Luo JW, Liu G, Zhu YB, Jin Z, Lin X. Lin XF, et al. Mol Med Rep. 2018 Nov;18(5):4271-4280. doi: 10.3892/mmr.2018.9455. Epub 2018 Sep 5. Mol Med Rep. 2018. PMID: 30221713 Free PMC article.
To study the familial gene-phenotype association, the exon and splice sites of 325 hereditary disease-associated genes in the proband with familial dilated cardiomyopathy (FDC), including 61 cardiac disease-associated genes, such as the lamins A/C (LMNA), were analy …
To study the familial gene-phenotype association, the exon and splice sites of 325 hereditary disease-associated genes in the proband …
Atrial Fibrillation Is an Independent Risk Factor for Hospital-Acquired Pneumonia.
Zhu J, Zhang X, Shi G, Yi K, Tan X. Zhu J, et al. PLoS One. 2015 Jul 23;10(7):e0131782. doi: 10.1371/journal.pone.0131782. eCollection 2015. PLoS One. 2015. PMID: 26204447 Free PMC article.
In our clinics, we have made empirical observation of such susceptibility. OBJECTIVES: To investigate the association between newly developed HAP and pre-existing AF, and to identify whether AF is an independent risk factor for HAP. ...Exclusion criteria were: havin …
In our clinics, we have made empirical observation of such susceptibility. OBJECTIVES: To investigate the association between …
Desmosomal junctions are necessary for adult sinus node function.
Mezzano V, Liang Y, Wright AT, Lyon RC, Pfeiffer E, Song MY, Gu Y, Dalton ND, Scheinman M, Peterson KL, Evans SM, Fowler S, Cerrone M, McCulloch AD, Sheikh F. Mezzano V, et al. Cardiovasc Res. 2016 Aug 1;111(3):274-86. doi: 10.1093/cvr/cvw083. Epub 2016 Apr 20. Cardiovasc Res. 2016. PMID: 27097650 Free PMC article.
Dysregulation of DSP via loss-of-function (adult DSP csKO mice) and mutation (clinical case of a patient harbouring a pathogenic DSP variant) in mice and man, respectively, revealed that desmosomal dysregulation is associated with a primary phenotype of increased sinus pau …
Dysregulation of DSP via loss-of-function (adult DSP csKO mice) and mutation (clinical case of a patient harbouring a pathogenic DSP variant …
Pacemaker activity of the human sinoatrial node: effects of HCN4 mutations on the hyperpolarization-activated current.
Verkerk AO, Wilders R. Verkerk AO, et al. Europace. 2014 Mar;16(3):384-95. doi: 10.1093/europace/eut348. Europace. 2014. PMID: 24569893 Review.
Since 2003, several loss-of-function mutations in the HCN4 gene, which encodes the HCN4 protein, or in the KCNE2 gene, which encodes the MiRP1 accessory beta-subunit, have been associated with sinus node dysfunction. Voltage-clamp experiments on HCN4 channels expressed in …
Since 2003, several loss-of-function mutations in the HCN4 gene, which encodes the HCN4 protein, or in the KCNE2 gene, which encodes the MiR …
Novel mutation in the alpha-myosin heavy chain gene is associated with sick sinus syndrome.
Ishikawa T, Jou CJ, Nogami A, Kowase S, Arrington CB, Barnett SM, Harrell DT, Arimura T, Tsuji Y, Kimura A, Makita N. Ishikawa T, et al. Circ Arrhythm Electrophysiol. 2015 Apr;8(2):400-8. doi: 10.1161/CIRCEP.114.002534. Epub 2015 Feb 25. Circ Arrhythm Electrophysiol. 2015. PMID: 25717017 Free article.
However, the existence of disease-causing MYH6 mutations for familial sick sinus syndrome and their underlying mechanisms remain unknown. METHODS AND RESULTS: We screened 9 genotype-negative probands with sick sinus syndrome famili …
However, the existence of disease-causing MYH6 mutations for familial sick sinus syndrome and their underlying m …
Cardiac Emerinopathy: A Nonsyndromic Nuclear Envelopathy With Increased Risk of Thromboembolic Stroke Due to Progressive Atrial Standstill and Left Ventricular Noncompaction.
Ishikawa T, Mishima H, Barc J, Takahashi MP, Hirono K, Terada S, Kowase S, Sato T, Mukai Y, Yui Y, Ohkubo K, Kimoto H, Watanabe H, Hata Y, Aiba T, Ohno S, Chishaki A, Shimizu W, Horie M, Ichida F, Nogami A, Yoshiura KI, Schott JJ, Makita N. Ishikawa T, et al. Circ Arrhythm Electrophysiol. 2020 Oct;13(10):e008712. doi: 10.1161/CIRCEP.120.008712. Epub 2020 Jul 29. Circ Arrhythm Electrophysiol. 2020. PMID: 32755394
METHODS: Targeted exon sequencing was performed in 87 probands with familial sick sinus syndrome (n=36) and a progressive cardiac conduction defect (n=51). RESULTS: We identified 3 X-linked recessive EMD mutations (start-loss, splicing, missense) in fa …
METHODS: Targeted exon sequencing was performed in 87 probands with familial sick sinus syndrome (n=36) and a progressi …
Genetic analysis of cardiac SCN5A Gene in Iranian patients with hereditary cardiac arrhythmias.
Asadi M, Foo R, Bhuiyan ZA, Samienasab MR, Salehi AR, Shahrzad S, Salehi R. Asadi M, et al. Anatol J Cardiol. 2016 Mar;16(3):170-4. doi: 10.5152/akd.2015.6060. Epub 2015 May 5. Anatol J Cardiol. 2016. PMID: 26467377 Free PMC article.
METHODS: Fifty-three members from three families each diagnosed with long-QT syndrome type 3 (LQTS3), Brugada syndrome (BrS), or sick sinus syndrome (SSS) were included in this observational, cross-sectional study. ...
METHODS: Fifty-three members from three families each diagnosed with long-QT syndrome type 3 (LQTS3), Brugada syndrome …
11 results