These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 26637293)

  • 21. Analysis of ACTA2 in European Moyamoya disease patients.
    Roder C; Peters V; Kasuya H; Nishizawa T; Wakita S; Berg D; Schulte C; Khan N; Tatagiba M; Krischek B
    Eur J Paediatr Neurol; 2011 Mar; 15(2):117-22. PubMed ID: 20970362
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Iris anomalies and the incidence of
    Taubenslag KJ; Scanga HL; Huey J; Lee J; Medsinge A; Sylvester CL; Cheng KP; Nischal KK
    Br J Ophthalmol; 2019 Apr; 103(4):499-503. PubMed ID: 29875232
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cerebrovascular Disease Progression in Patients With
    Lauer A; Speroni SL; Patel JB; Regalado E; Choi M; Smith E; Kalpathy-Kramer J; Caruso P; Milewicz DM; Musolino PL
    Neurology; 2021 Jan; 96(4):e538-e552. PubMed ID: 33199432
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cerebral arteriopathy in ACTA2 mutations: a spectrum of disease highlighted by a case of variable penetrance in two siblings.
    Tschoe C; Kim TE; Fargen KM; Wolfe SQ
    J Neurosurg Pediatr; 2021 Apr; 27(4):446-451. PubMed ID: 33513575
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Nuclear Smooth Muscle α-actin in Vascular Smooth Muscle Cell Differentiation.
    Kwartler CS; Pedroza AJ; Kaw A; Guan P; Ma S; Duan XY; Kernell C; Wang C; Pinelo JEE; Borthwick MS; Chen J; Zhong Y; Sinha S; Shen X; Fischbein MP; Milewicz DM
    Res Sq; 2023 Feb; ():. PubMed ID: 36909460
    [TBL] [Abstract][Full Text] [Related]  

  • 26. ACTA2 mutation with childhood cardiovascular, autonomic and brain anomalies and severe outcome.
    Meuwissen ME; Lequin MH; Bindels-de Heus K; Bruggenwirth HT; Knapen MF; Dalinghaus M; de Coo R; van Bever Y; Winkelman BH; Mancini GM
    Am J Med Genet A; 2013 Jun; 161A(6):1376-80. PubMed ID: 23613326
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Nuclear Smooth Muscle α-actin Participates in Vascular Smooth Muscle Cell Differentiation.
    Kwartler CS; Pedroza AJ; Kaw A; Guan P; Ma S; Duan XY; Kernell C; Wang C; Pinelo JEE; Bowen MSB; Chen J; Zhong Y; Sinha S; Shen X; Fischbein MP; Milewicz DM
    Nat Cardiovasc Res; 2023 Oct; 2(10):937-955. PubMed ID: 38919852
    [TBL] [Abstract][Full Text] [Related]  

  • 28.
    Yang WX; Zhang HH; Hu JN; Zhao L; Li YY; Shao XL
    World J Clin Cases; 2021 Oct; 9(29):8789-8796. PubMed ID: 34734057
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Expanding the Distinctive Neuroimaging Phenotype of
    D'Arco F; Alves CA; Raybaud C; Chong WKK; Ishak GE; Ramji S; Grima M; Barkovich AJ; Ganesan V
    AJNR Am J Neuroradiol; 2018 Nov; 39(11):2126-2131. PubMed ID: 30262641
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cardiac manifestations of human ACTA2 variants recapitulated in a zebrafish model.
    Sebastian WA; Inoue M; Shimizu N; Sato R; Oguri S; Itonaga T; Kishimoto S; Shiraishi H; Hanada T; Ihara K
    J Hum Genet; 2024 Apr; 69(3-4):133-138. PubMed ID: 38316882
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome.
    Roulez FM; Faes F; Delbeke P; Van Bogaert P; Rodesch G; De Zaeytijd J; Depasse F; Coucke PJ; Meire FM
    J Neuroophthalmol; 2014 Jun; 34(2):137-43. PubMed ID: 24621862
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Refractory cerebral infarction in a child with an ACTA2 mutation.
    Kanamori K; Sakaguchi Y; Tsuda K; Ihara S; Miyama S
    Brain Dev; 2021 Apr; 43(4):585-589. PubMed ID: 33342581
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Brachial artery occlusion in a young adult with an ACTA2 thoracic aortic aneurysm.
    Al-Mohaissen M; Allanson JE; O'Connor MD; Veinot JP; Brandys TM; Maharajh G; Dennie CJ; Beauchesne LM
    Vasc Med; 2012 Oct; 17(5):326-9. PubMed ID: 22946110
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cerebral arteriopathy associated with Arg179His ACTA2 mutation.
    Amans MR; Stout C; Fox C; Narvid J; Hetts SW; Cooke DL; Higashida RT; Dowd CF; McSwain H; Halbach VV
    J Neurointerv Surg; 2014 Nov; 6(9):e46. PubMed ID: 24353327
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital mydriasis and prune belly syndrome in a child with an ACTA2 mutation.
    Brodsky MC; Turan KE; Khanna CL; Patton A; Kirmani S
    J AAPOS; 2014 Aug; 18(4):393-5. PubMed ID: 24998021
    [TBL] [Abstract][Full Text] [Related]  

  • 36. ACTA2 mutation and postpartum hemorrhage: a case report.
    Cooper K; Brown S
    BMC Med Genet; 2017 Dec; 18(1):143. PubMed ID: 29202781
    [TBL] [Abstract][Full Text] [Related]  

  • 37. European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants.
    van de Laar IMBH; Arbustini E; Loeys B; Björck E; Murphy L; Groenink M; Kempers M; Timmermans J; Roos-Hesselink J; Benke K; Pepe G; Mulder B; Szabolcs Z; Teixidó-Turà G; Robert L; Emmanuel Y; Evangelista A; Pini A; von Kodolitsch Y; Jondeau G; De Backer J
    Orphanet J Rare Dis; 2019 Nov; 14(1):264. PubMed ID: 31752940
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A yeast based assay establishes the pathogenicity of novel missense ACTA2 variants associated with aortic aneurysms.
    Calderan C; Sorrentino U; Persano L; Trevisson E; Sartori G; Salviati L; Desbats MA
    Eur J Hum Genet; 2024 Jul; 32(7):804-812. PubMed ID: 38486025
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital Mydriasis With Aortic and Cerebrovascular Disease.
    Lam S; Guimaraes C; Jones JY
    Pediatr Neurol; 2017 Sep; 74():100-101. PubMed ID: 28647131
    [No Abstract]   [Full Text] [Related]  

  • 40. Cerebrovascular disease related to COL4A1 mutations in HANAC syndrome.
    Alamowitch S; Plaisier E; Favrole P; Prost C; Chen Z; Van Agtmael T; Marro B; Ronco P
    Neurology; 2009 Dec; 73(22):1873-82. PubMed ID: 19949034
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.