151 related articles for article (PubMed ID: 26927851)
1. Identification of Loci Modulating the Cardiovascular and Skeletal Phenotypes of Marfan Syndrome in Mice.
Fernandes GR; Massironi SM; Pereira LV
Sci Rep; 2016 Mar; 6():22426. PubMed ID: 26927851
[TBL] [Abstract][Full Text] [Related]
2. Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.
De Backer J
Verh K Acad Geneeskd Belg; 2009; 71(6):335-71. PubMed ID: 20232788
[TBL] [Abstract][Full Text] [Related]
3. Is HSPG2 a modifier gene for Marfan syndrome?
Gerdes Gyuricza I; Barbosa de Souza R; Farinha-Arcieri LE; Ribeiro Fernandes G; Veiga Pereira L
Eur J Hum Genet; 2020 Sep; 28(9):1292-1296. PubMed ID: 32514132
[TBL] [Abstract][Full Text] [Related]
4. A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression.
Lima BL; Santos EJ; Fernandes GR; Merkel C; Mello MR; Gomes JP; Soukoyan M; Kerkis A; Massironi SM; Visintin JA; Pereira LV
PLoS One; 2010 Nov; 5(11):e14136. PubMed ID: 21152435
[TBL] [Abstract][Full Text] [Related]
5. Genetic testing of the FBN1 gene in Chinese patients with Marfan/Marfan-like syndrome.
Yang H; Luo M; Chen Q; Fu Y; Zhang J; Qian X; Sun X; Fan Y; Zhou Z; Chang Q
Clin Chim Acta; 2016 Aug; 459():30-35. PubMed ID: 27234404
[TBL] [Abstract][Full Text] [Related]
6. Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome.
Rommel K; Karck M; Haverich A; von Kodolitsch Y; Rybczynski M; Müller G; Singh KK; Schmidtke J; Arslan-Kirchner M
Hum Mutat; 2005 Dec; 26(6):529-39. PubMed ID: 16220557
[TBL] [Abstract][Full Text] [Related]
7. Association of modifiers and other genetic factors explain Marfan syndrome clinical variability.
Aubart M; Gazal S; Arnaud P; Benarroch L; Gross MS; Buratti J; Boland A; Meyer V; Zouali H; Hanna N; Milleron O; Stheneur C; Bourgeron T; Desguerre I; Jacob MP; Gouya L; Génin E; Deleuze JF; Jondeau G; Boileau C
Eur J Hum Genet; 2018 Dec; 26(12):1759-1772. PubMed ID: 30087447
[TBL] [Abstract][Full Text] [Related]
8. Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies.
Robinson PN; Booms P; Katzke S; Ladewig M; Neumann L; Palz M; Pregla R; Tiecke F; Rosenberg T
Hum Mutat; 2002 Sep; 20(3):153-61. PubMed ID: 12203987
[TBL] [Abstract][Full Text] [Related]
9. Hyperkyphosis is not dependent on bone mass and quality in the mouse model of Marfan syndrome.
Souza RB; Kawahara EI; Farinha-Arcieri LE; Gyuricza IG; Neofiti-Papi B; Miranda-Rodrigues M; Teixeira MBCG; Fernandes GR; Lemes RB; Reinhardt DP; Gouveia CH; Pereira LV
Bone; 2021 Nov; 152():116073. PubMed ID: 34171513
[TBL] [Abstract][Full Text] [Related]
10. A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype.
Callea M; Eric Willoughby C; Camarata-Scalisi F; Giovannoni I; Vinciguerra A; Yavuz I; Di Stazio M; Di Iorio E; Clarich G; Benettoni A; Galeotti A; Bellacchio E
Invest Clin; 2017 Mar; 58(1):70-8. PubMed ID: 29939511
[TBL] [Abstract][Full Text] [Related]
11. Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24-32.
Maeda J; Kosaki K; Shiono J; Kouno K; Aeba R; Yamagishi H
Heart Vessels; 2016 Oct; 31(10):1717-23. PubMed ID: 26796135
[TBL] [Abstract][Full Text] [Related]
12. Marfan syndrome: Report of a complex phenotype due to a 15q21.1 contiguos gene deletion encompassing FBN1, and literature review.
Dordoni C; Ciaccio C; Santoro G; Venturini M; Cavallari U; Ritelli M; Colombi M
Am J Med Genet A; 2017 Jan; 173(1):200-206. PubMed ID: 27615407
[TBL] [Abstract][Full Text] [Related]
13. Recent progress towards a molecular understanding of Marfan syndrome.
Dietz HC; Loeys B; Carta L; Ramirez F
Am J Med Genet C Semin Med Genet; 2005 Nov; 139C(1):4-9. PubMed ID: 16273535
[TBL] [Abstract][Full Text] [Related]
14. FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutations.
Attanasio M; Lapini I; Evangelisti L; Lucarini L; Giusti B; Porciani M; Fattori R; Anichini C; Abbate R; Gensini G; Pepe G
Clin Genet; 2008 Jul; 74(1):39-46. PubMed ID: 18435798
[TBL] [Abstract][Full Text] [Related]
15. Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40.
Tiecke F; Katzke S; Booms P; Robinson PN; Neumann L; Godfrey M; Mathews KR; Scheuner M; Hinkel GK; Brenner RE; Hövels-Gürich HH; Hagemeier C; Fuchs J; Skovby F; Rosenberg T
Eur J Hum Genet; 2001 Jan; 9(1):13-21. PubMed ID: 11175294
[TBL] [Abstract][Full Text] [Related]
16. [The research progress in Marfan syndrome].
Zhu SH; Liu L
Fa Yi Xue Za Zhi; 2005 Feb; 21(1):58-60. PubMed ID: 15895810
[TBL] [Abstract][Full Text] [Related]
17. Pathophysiology and Management of Cardiovascular Manifestations in Marfan and Loeys-Dietz Syndromes.
Takeda N; Yagi H; Hara H; Fujiwara T; Fujita D; Nawata K; Inuzuka R; Taniguchi Y; Harada M; Toko H; Akazawa H; Komuro I
Int Heart J; 2016 May; 57(3):271-7. PubMed ID: 27181042
[TBL] [Abstract][Full Text] [Related]
18. Identification of FBN1 gene mutations in Ukrainian Marfan syndrome patients.
Zhurayev R; Proost D; Zerbino D; Fedorenko V; Meester JA; VAN Laer L; Loeys BL
Genet Res (Camb); 2016 Oct; 98():e13. PubMed ID: 27724990
[TBL] [Abstract][Full Text] [Related]
19. Marfan syndrome in the third Millennium.
Collod-Béroud G; Boileau C
Eur J Hum Genet; 2002 Nov; 10(11):673-81. PubMed ID: 12404097
[TBL] [Abstract][Full Text] [Related]
20. Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome.
Loeys B; De Backer J; Van Acker P; Wettinck K; Pals G; Nuytinck L; Coucke P; De Paepe A
Hum Mutat; 2004 Aug; 24(2):140-6. PubMed ID: 15241795
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
