BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 21892160)

  • 1. Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.
    de Pontual L; Yao E; Callier P; Faivre L; Drouin V; Cariou S; Van Haeringen A; Geneviève D; Goldenberg A; Oufadem M; Manouvrier S; Munnich A; Vidigal JA; Vekemans M; Lyonnet S; Henrion-Caude A; Ventura A; Amiel J
    Nat Genet; 2011 Sep; 43(10):1026-30. PubMed ID: 21892160
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A de novo 13q31.3 microduplication encompassing the miR-17 ~ 92 cluster results in features mirroring those associated with Feingold syndrome 2.
    Siavrienė E; Preikšaitienė E; Maldžienė Ž; Mikštienė V; Rančelis T; Ambrozaitytė L; Gueneau L; Reymond A; Kučinskas V
    Gene; 2020 Aug; 753():144816. PubMed ID: 32473250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2.
    Tassano E; Di Rocco M; Signa S; Gimelli G
    Am J Med Genet A; 2013 Apr; 161A(4):894-6. PubMed ID: 23495052
    [No Abstract]   [Full Text] [Related]  

  • 4. An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron.
    Han YC; Vidigal JA; Mu P; Yao E; Singh I; González AJ; Concepcion CP; Bonetti C; Ogrodowski P; Carver B; Selleri L; Betel D; Leslie C; Ventura A
    Nat Genet; 2015 Jul; 47(7):766-75. PubMed ID: 26029871
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neurobehavioral Alterations in a Genetic Murine Model of Feingold Syndrome 2.
    Fiori E; Babicola L; Andolina D; Coassin A; Pascucci T; Patella L; Han YC; Ventura A; Ventura R
    Behav Genet; 2015 Sep; 45(5):547-59. PubMed ID: 26026879
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q.
    Sirchia F; Di Gregorio E; Restagno G; Grosso E; Pappi P; Talarico F; Savin E; Cavalieri S; Giorgio E; Mancini C; Pasini B; Mehta JS; Brusco A
    Eur J Med Genet; 2017 Apr; 60(4):224-227. PubMed ID: 28159702
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Distinct molecular pathways mediate Mycn and Myc-regulated miR-17-92 microRNA action in Feingold syndrome mouse models.
    Mirzamohammadi F; Kozlova A; Papaioannou G; Paltrinieri E; Ayturk UM; Kobayashi T
    Nat Commun; 2018 Apr; 9(1):1352. PubMed ID: 29636449
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
    Cognet M; Nougayrede A; Malan V; Callier P; Cretolle C; Faivre L; Genevieve D; Goldenberg A; Heron D; Mercier S; Philip N; Sigaudy S; Verloes A; Sarnacki S; Munnich A; Vekemans M; Lyonnet S; Etchevers H; Amiel J; de Pontual L
    Eur J Hum Genet; 2011 May; 19(5):602-6. PubMed ID: 21224895
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic characterization of miR-92a-/- mice reveals an important function of miR-92a in skeletal development.
    Penzkofer D; Bonauer A; Fischer A; Tups A; Brandes RP; Zeiher AM; Dimmeler S
    PLoS One; 2014; 9(6):e101153. PubMed ID: 24979655
    [TBL] [Abstract][Full Text] [Related]  

  • 10. c-myc and N-myc promote active stem cell metabolism and cycling as architects of the developing brain.
    Wey A; Knoepfler PS
    Oncotarget; 2010 Jun; 1(2):120-30. PubMed ID: 20651942
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Feingold syndrome type 2 in a patient from China.
    Lei J; Han L; Huang Y; Long M; Zhao G; Yan S; Zhang J
    Am J Med Genet A; 2021 Jul; 185(7):2262-2266. PubMed ID: 33818875
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN.
    Burnside RD; Molinari S; Botti C; Brooks SS; Chung WK; Mehta L; Schwartz S; Papenhausen P
    Am J Med Genet A; 2018 Sep; 176(9):1956-1963. PubMed ID: 30088856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic factors in isolated and syndromic esophageal atresia.
    Geneviève D; de Pontual L; Amiel J; Lyonnet S
    J Pediatr Gastroenterol Nutr; 2011 May; 52 Suppl 1():S6-8. PubMed ID: 21499049
    [No Abstract]   [Full Text] [Related]  

  • 14. Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia.
    Brunner HG; Winter RM
    J Med Genet; 1991 Jun; 28(6):389-94. PubMed ID: 1870095
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a Rare Germline Heterozygous Deletion Involving the Polycistronic miR-17-92 Cluster in Two First-Degree Relatives from a BRCA 1/2 Negative Chilean Family with Familial Breast Cancer: Possible Functional Implications.
    de Mayo T; Ziegler A; Morales S; Jara L
    Int J Mol Sci; 2018 Jan; 19(1):. PubMed ID: 29361751
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GENETIC COUNSELLING IN FEINGOLD SYNDROME AND A NOVEL MUTATION.
    Atik T; Güvenç MS; Onay H; Özkinay F; Çoğulu Ö
    Genet Couns; 2016; 27(3):381-384. PubMed ID: 30204967
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.
    Chen CP; Lin SP; Chern SR; Wu PS; Chang SD; Ng SH; Liu YP; Su JW; Wang W
    Eur J Med Genet; 2012 Nov; 55(11):666-9. PubMed ID: 22842076
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A fourth case of Feingold syndrome type 2: psychiatric presentation and management.
    Ganjavi H; Siu VM; Speevak M; MacDonald PA
    BMJ Case Rep; 2014 Nov; 2014():. PubMed ID: 25391829
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2.
    Muriello M; Kim AY; Sondergaard Schatz K; Beck N; Gunay-Aygun M; Hoover-Fong JE
    Am J Med Genet A; 2019 Mar; 179(3):410-416. PubMed ID: 30672094
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?].
    Shongo MY; Lubala TK; Mbuyi SM; Makinko PI; Ngwej DT; Kabange FN
    Pan Afr Med J; 2012; 13():85. PubMed ID: 23396887
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.