BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 25255084)

  • 21. Decreasing
    Kean CM; Tracy CJ; Mitra A; Rahat B; Van Winkle MT; Gebert CM; Noeker JA; Calof AL; Lander AD; Kassis JA; Pfeifer K
    Sci Adv; 2022 Dec; 8(48):eadd4136. PubMed ID: 36449618
    [TBL] [Abstract][Full Text] [Related]  

  • 22. NIPBL
    Mills JA; Herrera PS; Kaur M; Leo L; McEldrew D; Tintos-Hernandez JA; Rajagopalan R; Gagne A; Zhang Z; Ortiz-Gonzalez XR; Krantz ID
    Sci Rep; 2018 Jan; 8(1):1056. PubMed ID: 29348408
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Connected Gene Communities Underlie Transcriptional Changes in Cornelia de Lange Syndrome.
    Boudaoud I; Fournier É; Baguette A; Vallée M; Lamaze FC; Droit A; Bilodeau S
    Genetics; 2017 Sep; 207(1):139-151. PubMed ID: 28679547
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Zebrafish as a Model to Study Cohesin and Cohesinopathies.
    Muto A; Schilling TF
    Methods Mol Biol; 2017; 1515():177-196. PubMed ID: 27797080
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe ipsilateral musculoskeletal involvement in a Cornelia de Lange patient with a novel NIPBL mutation.
    Baquero-Montoya C; Gil-Rodríguez MC; Hernández-Marcos M; Teresa-Rodrigo ME; Vicente-Gabas A; Bernal ML; Casale CH; Bueno-Lozano G; Bueno-Martínez I; Queralt E; Villa O; Hernando-Davalillo C; Armengol L; Gómez-Puertas P; Puisac B; Selicorni A; Ramos FJ; Pié J
    Eur J Med Genet; 2014 Sep; 57(9):503-9. PubMed ID: 24874887
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells.
    Gause M; Webber HA; Misulovin Z; Haller G; Rollins RA; Eissenberg JC; Bickel SE; Dorsett D
    Chromosoma; 2008 Feb; 117(1):51-66. PubMed ID: 17909832
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cohesin mediates chromatin interactions that regulate mammalian β-globin expression.
    Chien R; Zeng W; Kawauchi S; Bender MA; Santos R; Gregson HC; Schmiesing JA; Newkirk DA; Kong X; Ball AR; Calof AL; Lander AD; Groudine MT; Yokomori K
    J Biol Chem; 2011 May; 286(20):17870-8. PubMed ID: 21454523
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Defects of cohesin loader lead to bone dysplasia associated with transcriptional disturbance.
    Gu W; Wang L; Gu R; Ouyang H; Bao B; Zheng L; Xu B
    J Cell Physiol; 2021 Dec; 236(12):8208-8225. PubMed ID: 34170011
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Tri-phasic expression of posterior Hox genes during development of pectoral fins in zebrafish: implications for the evolution of vertebrate paired appendages.
    Ahn D; Ho RK
    Dev Biol; 2008 Oct; 322(1):220-33. PubMed ID: 18638469
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Prx1 limb enhancers: targeted gene expression in developing zebrafish pectoral fins.
    Hernández-Vega A; Minguillón C
    Dev Dyn; 2011 Aug; 240(8):1977-88. PubMed ID: 21674688
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients.
    Russo S; Masciadri M; Gervasini C; Azzollini J; Cereda A; Zampino G; Haas O; Scarano G; Di Rocco M; Finelli P; Tenconi R; Selicorni A; Larizza L
    Eur J Hum Genet; 2012 Jul; 20(7):734-41. PubMed ID: 22353942
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Latent developmental potential to form limb-like skeletal structures in zebrafish.
    Hawkins MB; Henke K; Harris MP
    Cell; 2021 Feb; 184(4):899-911.e13. PubMed ID: 33545089
    [TBL] [Abstract][Full Text] [Related]  

  • 33. NIPBL expression levels in CdLS probands as a predictor of mutation type and phenotypic severity.
    Kaur M; Mehta D; Noon SE; Deardorff MA; Zhang Z; Krantz ID
    Am J Med Genet C Semin Med Genet; 2016 Jun; 172(2):163-70. PubMed ID: 27125329
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Localisation of the SMC loading complex Nipbl/Mau2 during mammalian meiotic prophase I.
    Visnes T; Giordano F; Kuznetsova A; Suja JA; Lander AD; Calof AL; Ström L
    Chromosoma; 2014 Jun; 123(3):239-52. PubMed ID: 24287868
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neural crest cell-specific inactivation of Nipbl or Mau2 during mouse development results in a late onset of craniofacial defects.
    Smith TG; Laval S; Chen F; Rock MJ; Strachan T; Peters H
    Genesis; 2014 Jul; 52(7):687-94. PubMed ID: 24700590
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The Genome-Wide Impact of
    Spreafico M; Mangano E; Mazzola M; Consolandi C; Bordoni R; Battaglia C; Bicciato S; Marozzi A; Pistocchi A
    Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33352756
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome.
    Kuzniacka A; Wierzba J; Ratajska M; Lipska BS; Koczkowska M; Malinowska M; Limon J
    J Appl Genet; 2013 Feb; 54(1):27-33. PubMed ID: 23254390
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MAU2 and NIPBL Variants Impair the Heterodimerization of the Cohesin Loader Subunits and Cause Cornelia de Lange Syndrome.
    Parenti I; Diab F; Gil SR; Mulugeta E; Casa V; Berutti R; Brouwer RWW; Dupé V; Eckhold J; Graf E; Puisac B; Ramos F; Schwarzmayr T; Gines MM; van Staveren T; van IJcken WFJ; Strom TM; Pié J; Watrin E; Kaiser FJ; Wendt KS
    Cell Rep; 2020 May; 31(7):107647. PubMed ID: 32433956
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Gastrulation-stage gene expression in
    Chea S; Kreger J; Lopez-Burks ME; MacLean AL; Lander AD; Calof AL
    bioRxiv; 2024 Feb; ():. PubMed ID: 37905011
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Differential actinodin1 regulation in zebrafish and mouse appendages.
    Lalonde RL; Moses D; Zhang J; Cornell N; Ekker M; Akimenko MA
    Dev Biol; 2016 Sep; 417(1):91-103. PubMed ID: 27196393
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.