نتائج البحث

Analysis of circulating microRNAs in patients with repaired Tetralogy of Fallot with and without heart failure.

• Authors : Abu-Halima M; Department of Human Genetics, Saarland University, 66421, Homburg/Saar, Germany. .; Department of Human Genetics, Saarland University Medical Center, Kirrberger Straße 100, 66421, Homburg/Saar, Germany. .

Subjects: Circulating MicroRNA/Circulating MicroRNA/Circulating MicroRNA/*genetics ; Heart Failure/Heart Failure/Heart Failure/*blood ; Heart Failure/Heart Failure/Heart Failure/*genetics

• Source: Journal of translational medicine [J Transl Med] 2017 Jul 10; Vol. 15 (1), pp. 156. Date of Electronic Publication: 2017 Jul 10.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

تفاصيل العنوان

Analysis of circulating microRNAs in patients with repaired Tetralogy of Fallot with and without heart failure

• Authors : Masood Abu-Halima; Eckart Meese; Andreas Keller

Subjects: MicroRNA; Heart failure; Congenital heart defects

• Source: Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-13 (2017)

تفاصيل العنوان

Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD.

• Authors : Jaouadi H; Marseille Medical Genetics (MMG) U1251, Aix Marseille Université, INSERM, 13005, Marseille, France.; Jopling C

Subjects: Heart Defects, Congenital*/Heart Defects, Congenital*/Heart Defects, Congenital*/genetics ; Tetralogy of Fallot*; Adult

• Source: Journal of translational medicine [J Transl Med] 2023 Feb 28; Vol. 21 (1), pp. 160. Date of Electronic Publication: 2023 Feb 28.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Association of Promoter Methylation Statuses of Congenital Heart Defect Candidate genes with Tetralogy of Fallot.

• Authors : Wei Sheng^1,2 ; Yanyan Qian³ ; Ping Zhang²

• Source: Journal of Translational Medicine. 2014, Vol. 12 Issue 1, p1-22. 22p.

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Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypass.

• Authors : Raggi F; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.; Cangelosi D

Subjects: Heart Septal Defects, Atrial*/Heart Septal Defects, Atrial*/Heart Septal Defects, Atrial*/genetics ; Myocardium*/Myocardium*/Myocardium*/metabolism ; Tetralogy of Fallot*

• Source: Journal of translational medicine [J Transl Med] 2020 Jan 10; Vol. 18 (1), pp. 21. Date of Electronic Publication: 2020 Jan 10.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Analysis of circulating microRNAs in patients with repaired Tetralogy of Fallot with and without heart failure

• Authors : Tanja Rädle-Hurst; Eckart Meese; Hashim Abdul-Khaliq

Subjects: Adult; Male; 0301 basic medicine

• Source: Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-13 (2017)Journal of Translational Medicine

تفاصيل العنوان

Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.

• Authors : Yanyan Qian; Deyong Xiao; Xiao Guo

Subjects: CONGENITAL heart disease; HUMAN abnormalities; IMMUNOPRECIPITATION

• Source: Journal of Translational Medicine; 4/3/2017, Vol. 15, p1-14, 14p

تفاصيل العنوان

Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.

• Authors : Qian Y; Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, Department of Biochemistry and Molecular Biology, Collaborative Innovation Center of Genetics and Development, Institutes of Biomedical Sciences, School of Basic Medical Sciences, Fudan University, Shanghai, 20032, China.; Shanghai Key Lab of Birth Defect, Children's Hospital of Fudan University, Shanghai, 201102, China.

Subjects: Gene Expression Regulation* ; Genetic Variation* ; Transcription, Genetic*

• Source: Journal of translational medicine [J Transl Med] 2017 Apr 03; Vol. 15 (1), pp. 69. Date of Electronic Publication: 2017 Apr 03.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

تفاصيل العنوان

Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation

• Authors : Duan Ma; Xiao Guo; Huijun Wang

Subjects: Heart Defects, Congenital; Male; Transcriptional Activation

• Source: Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-14 (2017)Journal of Translational Medicine

تفاصيل العنوان

Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD

• Authors : Hager Jaouadi; Chris Jopling; Fanny Bajolle

Subjects: Congenital heart defects; Robo-Slit pathway; Genetics

• Source: Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-10 (2023)

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