103 related articles for article (PubMed ID: 35154271)
1. Rare Variants and Polymorphisms of
Pan M; Li L; Li Z; Chen S; Li Z; Wang Y; He H; Lin L; Wang H; Liu Q
Front Genet; 2022; 13():778806. PubMed ID: 35154271
[TBL] [Abstract][Full Text] [Related]
2. Association of gene polymorphisms in FBN1 and TGF-β signaling with the susceptibility and prognostic outcomes of Stanford type B aortic dissection.
Sun L; Chang Y; Jiang P; Ma Y; Yuan Q; Ma X
BMC Med Genomics; 2022 Mar; 15(1):65. PubMed ID: 35307021
[TBL] [Abstract][Full Text] [Related]
3. FBN1 mutations largely contribute to sporadic non-syndromic aortic dissection.
Tan L; Li Z; Zhou C; Cao Y; Zhang L; Li X; Cianflone K; Wang Y; Wang DW
Hum Mol Genet; 2017 Dec; 26(24):4814-4822. PubMed ID: 28973303
[TBL] [Abstract][Full Text] [Related]
4. Exploring the genetic pathogenicity of aortic dissection from 72 Han Chinese individuals using next-generation sequencing.
Pan M; Chen S; Wang H; Wu S; Ding Z; Wang Y; Li L; Li Z; Liu Q
Clin Genet; 2020 May; 97(5):704-711. PubMed ID: 32154576
[TBL] [Abstract][Full Text] [Related]
5. Association of MLL3 and TGF-β signaling gene polymorphisms with the susceptibility and prognostic outcomes of Stanford type B aortic dissection : MLL3 with TGF-β signal pathway association with Stanford type B AD.
Yuan Q; Chang Y; Jiang P; Sun L; Ma Y; Ma X
BMC Cardiovasc Disord; 2023 May; 23(1):275. PubMed ID: 37226099
[TBL] [Abstract][Full Text] [Related]
6. Acute Stanford type B aortic dissection-who benefits from genetic testing?
Erhart P; Gieldon L; Ante M; Körfer D; Strom T; Grond-Ginsbach C; Böckler D
J Thorac Dis; 2020 Nov; 12(11):6806-6812. PubMed ID: 33282382
[TBL] [Abstract][Full Text] [Related]
7. Fibrillin-1 Gene Polymorphisms (rs145233125, rs11070646, rs201170905) Are Associated With the Susceptibility and Clinical Prognosis of DeBakey Type III Aortic Dissection in Chinese Han Population.
Sun L; Chang Y; Jiang P; Wang B; Ma Y; Yuan Q; Ma X
J Cardiovasc Pharmacol; 2022 Jul; 80(1):118-124. PubMed ID: 35500095
[TBL] [Abstract][Full Text] [Related]
8. Genetic variants in Chinese patients with sporadic Stanford type A aortic dissection.
Chen ZR; Bao MH; Wang XY; Yang YM; Huang B; Han ZL; Cai J; Fan XH
J Thorac Dis; 2021 Jul; 13(7):4008-4022. PubMed ID: 34422331
[TBL] [Abstract][Full Text] [Related]
9. A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum.
Peng Q; Deng Y; Yang Y; Liu H
BMC Pediatr; 2016 Apr; 16():60. PubMed ID: 27138491
[TBL] [Abstract][Full Text] [Related]
10. Decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants.
Baudhuin LM; Kotzer KE; Lagerstedt SA
J Hum Genet; 2015 May; 60(5):241-52. PubMed ID: 25652356
[TBL] [Abstract][Full Text] [Related]
11. Variability in gene-based knowledge impacts variant classification: an analysis of FBN1 missense variants in ClinVar.
Baudhuin LM; Kluge ML; Kotzer KE; Lagerstedt SA
Eur J Hum Genet; 2019 Oct; 27(10):1550-1560. PubMed ID: 31227806
[TBL] [Abstract][Full Text] [Related]
12. Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
Stengl R; Bors A; Ágg B; Pólos M; Matyas G; Molnár MJ; Fekete B; Csabán D; Andrikovics H; Merkely B; Radovits T; Szabolcs Z; Benke K
Orphanet J Rare Dis; 2020 Oct; 15(1):290. PubMed ID: 33059708
[TBL] [Abstract][Full Text] [Related]
13. Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.
Cecchi A; Ogawa N; Martinez HR; Carlson A; Fan Y; Penny DJ; Guo DC; Eisenberg S; Safi H; Estrera A; Lewis RA; Meyers D; Milewicz DM
Am J Med Genet A; 2013 Sep; 161A(9):2305-10. PubMed ID: 23897642
[TBL] [Abstract][Full Text] [Related]
14. Type A aortic dissection in pregnant patients with fibrillin-1 gene mutations: Two case reports and a literature review.
Lei Y; Jiang Z; Chen J; Wang D; Hong G; Chen S
Exp Ther Med; 2018 Dec; 16(6):4407-4414. PubMed ID: 30542390
[TBL] [Abstract][Full Text] [Related]
15. FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies.
Madar L; Szakszon K; Pfliegler G; Szabó GP; Brúgós B; Ronen N; Papp J; Zahuczky K; Szakos E; Fekete G; Oláh É; Koczok K; Balogh I
J Biotechnol; 2019 Aug; 301():105-111. PubMed ID: 31163209
[TBL] [Abstract][Full Text] [Related]
16. Classification and Interpretation for 11 FBN1 Variants Responsible for Marfan Syndrome and Pre-implantation Genetic Testing (PGT) for Two Families Successfully Blocked Transmission of the Pathogenic Mutations.
Chen S; Fei H; Zhang J; Chen Y; Huang H; Lu D; Xu C
Front Mol Biosci; 2021; 8():749842. PubMed ID: 34957211
[No Abstract] [Full Text] [Related]
17. Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China.
Li Y; Fang M; Yang J; Yu C; Kuang J; Sun T; Fan R
Am J Transl Res; 2021; 13(5):4281-4295. PubMed ID: 34150014
[TBL] [Abstract][Full Text] [Related]
18. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.
Haller G; Alvarado DM; Willing MC; Braverman AC; Bridwell KH; Kelly M; Lenke LG; Luhmann SJ; Gurnett CA; Dobbs MB
J Bone Joint Surg Am; 2015 Sep; 97(17):1411-7. PubMed ID: 26333736
[TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
Mannucci L; Luciano S; Salehi LB; Gigante L; Conte C; Longo G; Ferradini V; Piumelli N; Brancati F; Ruvolo G; Novelli G; Sangiuolo F
Clin Chim Acta; 2020 Feb; 501():154-164. PubMed ID: 31730815
[TBL] [Abstract][Full Text] [Related]
20. Association between
Sepetiene R; Patamsyte V; Zukovas G; Jariene G; Stanioniene Z; Benetis R; Tamosiunas A; Lesauskaite V
Mol Med; 2015 Nov; 21(1):735-738. PubMed ID: 26322848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
