BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 35094088)

  • 1. NSD1 mutations deregulate transcription and DNA methylation of bivalent developmental genes in Sotos syndrome.
    Brennan K; Zheng H; Fahrner JA; Shin JH; Gentles AJ; Schaefer B; Sunwoo JB; Bernstein JA; Gevaert O
    Hum Mol Genet; 2022 Jul; 31(13):2164-2184. PubMed ID: 35094088
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.
    Watanabe H; Higashimoto K; Miyake N; Morita S; Horii T; Kimura M; Suzuki T; Maeda T; Hidaka H; Aoki S; Yatsuki H; Okamoto N; Uemura T; Hatada I; Matsumoto N; Soejima H
    FASEB J; 2020 Jan; 34(1):960-973. PubMed ID: 31914674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NSD1 mutations generate a genome-wide DNA methylation signature.
    Choufani S; Cytrynbaum C; Chung BH; Turinsky AL; Grafodatskaya D; Chen YA; Cohen AS; Dupuis L; Butcher DT; Siu MT; Luk HM; Lo IF; Lam ST; Caluseriu O; Stavropoulos DJ; Reardon W; Mendoza-Londono R; Brudno M; Gibson WT; Chitayat D; Weksberg R
    Nat Commun; 2015 Dec; 6():10207. PubMed ID: 26690673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Epigenetic inactivation of the Sotos overgrowth syndrome gene histone methyltransferase NSD1 in human neuroblastoma and glioma.
    Berdasco M; Ropero S; Setien F; Fraga MF; Lapunzina P; Losson R; Alaminos M; Cheung NK; Rahman N; Esteller M
    Proc Natl Acad Sci U S A; 2009 Dec; 106(51):21830-5. PubMed ID: 20018718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-Wide DNA Methylation Profiling Solves Uncertainty in Classifying
    Ferilli M; Ciolfi A; Pedace L; Niceta M; Radio FC; Pizzi S; Miele E; Cappelletti C; Mancini C; Galluccio T; Andreani M; Iascone M; Chiriatti L; Novelli A; Micalizzi A; Matraxia M; Menale L; Faletra F; Prontera P; Pilotta A; Bedeschi MF; Capolino R; Baban A; Seri M; Mammì C; Zampino G; Digilio MC; Dallapiccola B; Priolo M; Tartaglia M
    Genes (Basel); 2022 Nov; 13(11):. PubMed ID: 36421837
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromatin regulation of transcriptional enhancers and cell fate by the Sotos syndrome gene NSD1.
    Sun Z; Lin Y; Islam MT; Koche R; Hedehus L; Liu D; Huang C; Vierbuchen T; Sawyers CL; Helin K
    Mol Cell; 2023 Jul; 83(14):2398-2416.e12. PubMed ID: 37402365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The first pineoblastoma case report of a patient with Sotos syndrome harboring NSD1 germline mutation.
    Yue X; Liu B; Han T; Guo D; Ding R; Wang G
    BMC Pediatr; 2024 Mar; 24(1):166. PubMed ID: 38459438
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1.
    Martin-Herranz DE; Aref-Eshghi E; Bonder MJ; Stubbs TM; Choufani S; Weksberg R; Stegle O; Sadikovic B; Reik W; Thornton JM
    Genome Biol; 2019 Aug; 20(1):146. PubMed ID: 31409373
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.
    Conteduca G; Testa B; Baldo C; Arado A; Malacarne M; Candiano G; Garbarino A; Coviello DA; Cantoni C
    Gene; 2023 Jan; 851():146970. PubMed ID: 36261088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in SETD2 cause a novel overgrowth condition.
    Luscan A; Laurendeau I; Malan V; Francannet C; Odent S; Giuliano F; Lacombe D; Touraine R; Vidaud M; Pasmant E; Cormier-Daire V
    J Med Genet; 2014 Aug; 51(8):512-7. PubMed ID: 24852293
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1.
    Oishi S; Zalucki O; Vega MS; Harkins D; Harvey TJ; Kasherman M; Davila RA; Hale L; White M; Piltz S; Thomas P; Burne THJ; Harris L; Piper M
    Genes Brain Behav; 2020 Apr; 19(4):e12637. PubMed ID: 31909872
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel nonsense variant in NSD1 gene in a female child with Sotos syndrome: A case report and literature review.
    Liu X; Chen C; Wan L; Zhu G; Zhao Y; Hu L; Liang Y; Gao J; Wang J; Yang G
    Brain Behav; 2023 Dec; 13(12):e3290. PubMed ID: 37908045
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of Novel NSD1 variations in four Pediatric cases with sotos Syndrome.
    Ren Z; Yue L; Hu HY; Hou XL; Chen WQ; Tan Y; Dong Z; Zhang J
    BMC Med Genomics; 2024 Apr; 17(1):116. PubMed ID: 38684994
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Su X; Zhang J; Mouawad R; Compérat E; Rouprêt M; Allanic F; Parra J; Bitker MO; Thompson EJ; Gowrishankar B; Houldsworth J; Weinstein JN; Tost J; Broom BM; Khayat D; Spano JP; Tannir NM; Malouf GG
    Cancer Res; 2017 Sep; 77(18):4835-4845. PubMed ID: 28754676
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations.
    Grand K; Gonzalez-Gandolfi C; Ackermann AM; Aljeaid D; Bedoukian E; Bird LM; De Leon DD; Diaz J; Hopkin RJ; Kadakia SP; Keena B; Klein KO; Krantz I; Leon E; Lord K; McDougall C; Medne L; Skraban CM; Stanley CA; Tarpinian J; Zackai E; Deardorff MA; Kalish JM
    Am J Med Genet A; 2019 Apr; 179(4):542-551. PubMed ID: 30719864
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Histone methylation mediated by NSD1 is required for the establishment and maintenance of neuronal identities.
    Zheng Y; Zhao C; Song Q; Xu L; Zhang B; Hu G; Kong X; Li S; Li X; Shen Y; Zhuang L; Wu M; Liu Y; Zhou Y
    Cell Rep; 2023 Dec; 42(12):113496. PubMed ID: 37995181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hypoparathyroidism in a 3-year-old Korean boy with Sotos syndrome and a novel mutation in NSD1.
    Wejaphikul K; Cho SY; Huh R; Kwun Y; Lee J; Ki CS; Jin DK
    Ann Clin Lab Sci; 2015; 45(2):215-8. PubMed ID: 25887879
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NSD1 gene evolves under episodic selection within primates and mutations of specific exons in humans cause Sotos syndrome.
    Romero VI; Arias-Almeida B; Aguiar SA
    BMC Genomics; 2022 Dec; 23(1):849. PubMed ID: 36550402
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First identified Korean family with Sotos syndrome caused by a novel intragenic mutation in NSD1.
    Park SH; Lee JE; Sohn YB; Ko JM
    Ann Clin Lab Sci; 2014; 44(2):228-31. PubMed ID: 24795065
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The histone mark H3K36me2 recruits DNMT3A and shapes the intergenic DNA methylation landscape.
    Weinberg DN; Papillon-Cavanagh S; Chen H; Yue Y; Chen X; Rajagopalan KN; Horth C; McGuire JT; Xu X; Nikbakht H; Lemiesz AE; Marchione DM; Marunde MR; Meiners MJ; Cheek MA; Keogh MC; Bareke E; Djedid A; Harutyunyan AS; Jabado N; Garcia BA; Li H; Allis CD; Majewski J; Lu C
    Nature; 2019 Sep; 573(7773):281-286. PubMed ID: 31485078
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.