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 *

230 related articles for article (PubMed ID: 35230976)

  • 41. Increased osteoclastogenesis contributes to bone loss in the Costello syndrome
    Nandi S; Chennappan S; Andrasch Y; Fidan M; Engler M; Ahmad M; Tuckermann JP; Zenker M; Cirstea IC
    Front Cell Dev Biol; 2022; 10():1000575. PubMed ID: 36330334
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Somatic mosaicism for an HRAS mutation causes Costello syndrome.
    Gripp KW; Stabley DL; Nicholson L; Hoffman JD; Sol-Church K
    Am J Med Genet A; 2006 Oct; 140(20):2163-9. PubMed ID: 16969868
    [TBL] [Abstract][Full Text] [Related]  

  • 43.
    Rodríguez NA; Patel N; Dariolli R; Ng S; Aleman AG; Gong JQX; Lin HM; Rodríguez M; Josowitz R; Sol-Church K; Gripp KW; Lin X; Song SC; Fishman GI; Sobie EA; Gelb BD
    Circ Arrhythm Electrophysiol; 2024 Apr; 17(4):e012022. PubMed ID: 38415356
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A very mild phenotype in six individuals of a three-generation family with the novel HRAS variant c.176C > G p.(Ala59Gly): Emergence of a new HRAS-related RASopathy distinct from Costello syndrome.
    Frey T; Ivanovski I; Bahr A; Zweier M; Laube J; Luchsinger I; Steindl K; Rauch A
    Am J Med Genet A; 2023 Aug; 191(8):2074-2082. PubMed ID: 37194190
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Differential Effects of HRAS Mutation on LTP-Like Activity Induced by Different Protocols of Repetitive Transcranial Magnetic Stimulation.
    Dileone M; Ranieri F; Florio L; Capone F; Musumeci G; Leoni C; Mordillo-Mateos L; Tartaglia M; Zampino G; Di Lazzaro V
    Brain Stimul; 2016; 9(1):33-8. PubMed ID: 26419841
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phenotypic analysis of individuals with Costello syndrome due to HRAS p.G13C.
    Gripp KW; Hopkins E; Sol-Church K; Stabley DL; Axelrad ME; Doyle D; Dobyns WB; Hudson C; Johnson J; Tenconi R; Graham GE; Sousa AB; Heller R; Piccione M; Corsello G; Herman GE; Tartaglia M; Lin AE
    Am J Med Genet A; 2011 Apr; 155A(4):706-16. PubMed ID: 21438134
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Respiratory system involvement in Costello syndrome.
    Gomez-Ospina N; Kuo C; Ananth AL; Myers A; Brennan ML; Stevenson DA; Bernstein JA; Hudgins L
    Am J Med Genet A; 2016 Jul; 170(7):1849-57. PubMed ID: 27102959
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Clinical, pathological, and molecular analyses of cardiovascular abnormalities in Costello syndrome: a Ras/MAPK pathway syndrome.
    Lin AE; Alexander ME; Colan SD; Kerr B; Rauen KA; Noonan J; Baffa J; Hopkins E; Sol-Church K; Limongelli G; Digilio MC; Marino B; Innes AM; Aoki Y; Silberbach M; Delrue MA; White SM; Hamilton RM; O'Connor W; Grossfeld PD; Smoot LB; Padera RF; Gripp KW
    Am J Med Genet A; 2011 Mar; 155A(3):486-507. PubMed ID: 21344638
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Behavioral phenotype in Costello syndrome with atypical mutation: a case report.
    Alfieri P; Caciolo C; Piccini G; D'Elia L; Valeri G; Menghini D; Tartaglia M; Digilio MC; Dallapiccola B; Vicari S
    Am J Med Genet B Neuropsychiatr Genet; 2015 Jan; 168B(1):66-71. PubMed ID: 25367099
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Excess of neuromuscular spindles in a fetus with Costello syndrome: a clinicopathological report.
    Sinico M; Bassez G; Touboul C; Cavé H; Vergnaud A; Zirah C; Fleury-Feith J; Gettler S; Vojtek AM; Chevalier N; Amram D; Alsamad IA; Haddad B; Encha-Razavi F
    Pediatr Dev Pathol; 2011; 14(3):218-23. PubMed ID: 20658932
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Ophthalmic manifestations in Costello syndrome caused by Ras pathway dysregulation during development.
    Shankar SP; Fallurin R; Watson T; Shankar PR; Young TL; Orel-Bixler D; Rauen KA
    Ophthalmic Genet; 2022 Feb; 43(1):48-57. PubMed ID: 34612139
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A novel patient with an attenuated Costello syndrome phenotype due to an HRAS mutation affecting codon 146-Literature review and update.
    Chiu AT; Leung GK; Chu YW; Gripp KW; Chung BH
    Am J Med Genet A; 2017 Apr; 173(4):1109-1114. PubMed ID: 28328122
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma.
    Robbins KM; Stabley DL; Holbrook J; Sahraoui R; Sadreameli A; Conard K; Baker L; Gripp KW; Sol-Church K
    Am J Med Genet A; 2016 Dec; 170(12):3197-3206. PubMed ID: 27589201
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Recurring G12S mutation of HRAS in a Chinese child with Costello syndrome with high alkaline phosphatase level.
    Zhang H; Ye J; Gu X
    Biochem Genet; 2009 Dec; 47(11-12):868-72. PubMed ID: 19669404
    [No Abstract]   [Full Text] [Related]  

  • 55. The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.
    Hiippala A; Vasilescu C; Tallila J; Alastalo TP; Paetau A; Tyni T; Suomalainen A; Euro L; Ojala T
    Am J Med Genet A; 2016 Jun; 170(6):1433-8. PubMed ID: 26888048
    [TBL] [Abstract][Full Text] [Related]  

  • 56. HRAS and the Costello syndrome.
    Rauen KA
    Clin Genet; 2007 Feb; 71(2):101-8. PubMed ID: 17250658
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies.
    Leung GKC; Luk HM; Tang VHM; Gao WW; Mak CCY; Yu MHC; Wong WL; Chu YWY; Yang WL; Wong WHS; Ma ACH; Leung AYH; Jin DY; Chan KYK; Allanson J; Lo IFM; Chung BHY
    Sci Rep; 2018 Feb; 8(1):2421. PubMed ID: 29402968
    [TBL] [Abstract][Full Text] [Related]  

  • 58. The novel duplication HRAS c.186_206dup p.(Glu62_Arg68dup): clinical and functional aspects.
    Gripp KW; Baker L; Robbins KM; Stabley DL; Bellus GA; Kolbe V; Nauth T; Rosenberger G
    Eur J Hum Genet; 2020 Nov; 28(11):1548-1554. PubMed ID: 32499600
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The role of p19 and p21 H-Ras proteins and mutants in miRNA expression in cancer and a Costello syndrome cell model.
    García-Cruz R; Camats M; Calin GA; Liu CG; Volinia S; Taccioli C; Croce CM; Bach-Elias M
    BMC Med Genet; 2015 Jul; 16():46. PubMed ID: 26138095
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Comprehensive genetic analysis of overlapping syndromes of RAS/RAF/MEK/ERK pathway.
    Tumurkhuu M; Saitoh M; Sato A; Takahashi K; Mimaki M; Takita J; Takeshita K; Hama T; Oka A; Mizuguchi M
    Pediatr Int; 2010 Aug; 52(4):557-62. PubMed ID: 20030748
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.