BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 21892160)

  • 21. Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster.
    Hemmat M; Rumple MJ; Mahon LW; Strom CM; Anguiano A; Talai M; Nguyen B; Boyar FZ
    Mol Cytogenet; 2014; 7():27. PubMed ID: 24739087
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exudative retinopathy, cerebral calcifications, duodenal atresia, preaxial polydactyly, micropenis, microcephaly and short stature: a new syndrome?
    Isidor B; Le Meur G; Conti C; Caldagues E; Lainey E; Launay E; Leclair MD; Le Francois T; Pichon O; Boisseau P; Migraine A; Keren B; Le Caignec C; Crow YJ; David A
    Am J Med Genet A; 2013 Aug; 161A(8):1829-32. PubMed ID: 23824919
    [TBL] [Abstract][Full Text] [Related]  

  • 23. How many entities exist for the spectrum of disorders associated with brachydactyly, syndactyly, short stature, microcephaly, and intellectual disability?
    Ravel A; Chouery E; Stora S; Jalkh N; Villard L; Temtamy S; Mégarbané A
    Am J Med Genet A; 2011 Apr; 155A(4):880-4. PubMed ID: 21416592
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype.
    Tedesco MG; Lonardo F; Ceccarini C; Cesarano C; Digilio MC; Magliozzi M; Rogaia D; Mencarelli A; Leoni C; Piscopo C; Imperatore V; Falco MT; Fontana P; Nardone AM; Novelli A; Troiani S; Seri M; Prontera P
    Am J Med Genet A; 2021 Apr; 185(4):1204-1210. PubMed ID: 33442900
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.
    Yu X; Hu L; Liu X; Zhan G; Mei M; Wang H; Zhang X; Qiu Z; Zhou W; Yang L
    Neurosci Bull; 2018 Oct; 34(5):854-858. PubMed ID: 29786759
    [No Abstract]   [Full Text] [Related]  

  • 26. Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature.
    Shaw-Smith C
    Eur J Med Genet; 2010; 53(1):6-13. PubMed ID: 19822228
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial syndromic esophageal atresia maps to 2p23-p24.
    Celli J; van Beusekom E; Hennekam RC; Gallardo ME; Smeets DF; de Córdoba SR; Innis JW; Frydman M; König R; Kingston H; Tolmie J; Govaerts LC; van Bokhoven H; Brunner HG
    Am J Hum Genet; 2000 Feb; 66(2):436-44. PubMed ID: 10677303
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities.
    Koufaris C; Papagregoriou G; Kousoulidou L; Moutafi M; Tauber M; Jouret B; Kieffer I; Deltas C; Tanteles GA; Anastasiadou V; Patsalis PC; Sismani C
    Gene; 2015 Apr; 561(1):95-100. PubMed ID: 25680557
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Detection of a de novo interstitial 2q microdeletion by CGH microarray analysis in a patient with limb malformations, microcephaly and mental retardation.
    Svensson AM; Curry CJ; South ST; Whitby H; Maxwell TM; Aston E; Fisher J; Carmack CE; Scheffer A; Abu-Shamsieh A; Brothman AR
    Am J Med Genet A; 2007 Jun; 143A(12):1348-53. PubMed ID: 17506097
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic dissection of the miR-17~92 cluster of microRNAs in Myc-induced B-cell lymphomas.
    Mu P; Han YC; Betel D; Yao E; Squatrito M; Ogrodowski P; de Stanchina E; D'Andrea A; Sander C; Ventura A
    Genes Dev; 2009 Dec; 23(24):2806-11. PubMed ID: 20008931
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Two miRNA clusters, miR-34b/c and miR-449, are essential for normal brain development, motile ciliogenesis, and spermatogenesis.
    Wu J; Bao J; Kim M; Yuan S; Tang C; Zheng H; Mastick GS; Xu C; Yan W
    Proc Natl Acad Sci U S A; 2014 Jul; 111(28):E2851-7. PubMed ID: 24982181
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Expanding the phenotype of feingold syndrome-2.
    Grote LE; Repnikova EA; Amudhavalli SM
    Am J Med Genet A; 2015 Dec; 167A(12):3219-25. PubMed ID: 26360630
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Origin, evolution, and biological role of miRNA cluster in DLK-DIO3 genomic region in placental mammals.
    Glazov EA; McWilliam S; Barris WC; Dalrymple BP
    Mol Biol Evol; 2008 May; 25(5):939-48. PubMed ID: 18281269
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome.
    Nishio Y; Kato K; Tran Mau-Them F; Futagawa H; Quélin C; Masuda S; Vitobello A; Otsuji S; Shawki HH; Oishi H; Thauvin-Robinet C; Takenouchi T; Kosaki K; Takahashi Y; Saitoh S
    HGG Adv; 2023 Oct; 4(4):100238. PubMed ID: 37710961
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel regulation and functional interaction of polycistronic miRNAs.
    Truscott M; Islam AB; Frolov MV
    RNA; 2016 Jan; 22(1):129-38. PubMed ID: 26554028
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Esophageal atresia with tracheoesophageal fistula in a patient with 7q35-36.3 deletion including SHH gene.
    Busa T; Panait N; Chaumoitre K; Philip N; Missirian C
    Eur J Med Genet; 2016 Oct; 59(10):546-8. PubMed ID: 27614115
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.
    Barøy T; Misceo D; Strømme P; Stray-Pedersen A; Holmgren A; Rødningen OK; Blomhoff A; Helle JR; Stormyr A; Tvedt B; Fannemel M; Frengen E
    Orphanet J Rare Dis; 2013 Jan; 8():3. PubMed ID: 23294540
    [TBL] [Abstract][Full Text] [Related]  

  • 38. miRNA mutations are not a common cause of deafness.
    Hildebrand MS; Witmer PD; Xu S; Newton SS; Kahrizi K; Najmabadi H; Valle D; Smith RJ
    Am J Med Genet A; 2010 Mar; 152A(3):646-52. PubMed ID: 20186779
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Functional links between clustered microRNAs: suppression of cell-cycle inhibitors by microRNA clusters in gastric cancer.
    Kim YK; Yu J; Han TS; Park SY; Namkoong B; Kim DH; Hur K; Yoo MW; Lee HJ; Yang HK; Kim VN
    Nucleic Acids Res; 2009 Apr; 37(5):1672-81. PubMed ID: 19153141
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.
    Sabina S; Pulignani S; Rizzo M; Cresci M; Vecoli C; Foffa I; Ait-Ali L; Pitto L; Andreassi MG
    J Mol Cell Cardiol; 2013 Jul; 60():84-9. PubMed ID: 23583740
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.