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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

114 related items for PubMed ID: 17127446

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. A molecular pathogenesis for transcription factor associated poly-alanine tract expansions.
    Albrecht AN, Kornak U, Böddrich A, Süring K, Robinson PN, Stiege AC, Lurz R, Stricker S, Wanker EE, Mundlos S.
    Hum Mol Genet; 2004 Oct 15; 13(20):2351-9. PubMed ID: 15333588
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism.
    Alatzoglou KS, Kelberman D, Cowell CT, Palmer R, Arnhold IJ, Melo ME, Schnabel D, Grueters A, Dattani MT.
    J Clin Endocrinol Metab; 2011 Apr 15; 96(4):E685-90. PubMed ID: 21289259
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Increased transactivation and impaired repression of β-catenin-mediated transcription associated with a novel SOX3 missense mutation in an X-linked hypopituitarism pedigree with modest growth failure.
    Yu T, Chang G, Cheng Q, Yao R, Li J, Xu Y, Li G, Ding Y, Qing Y, Li N, Shen Y, Wang X, Wang J.
    Mol Cell Endocrinol; 2018 Dec 15; 478():133-140. PubMed ID: 30125608
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome.
    Di Lascio S, Bachetti T, Saba E, Ceccherini I, Benfante R, Fornasari D.
    Neurobiol Dis; 2013 Feb 15; 50():187-200. PubMed ID: 23103552
    [Abstract] [Full Text] [Related]

  • 10. A novel mutation in SOX3 polyalanine tract: a case of Kabuki syndrome with combined pituitary hormone deficiency harboring double mutations in MLL2 and SOX3.
    Takagi M, Ishii T, Torii C, Kosaki K, Hasegawa T.
    Pituitary; 2014 Dec 15; 17(6):569-74. PubMed ID: 24346842
    [Abstract] [Full Text] [Related]

  • 11. Functional characterization of the human SOX3 promoter: identification of transcription factors implicated in basal promoter activity.
    Kovacevic Grujicic N, Mojsin M, Krstic A, Stevanovic M.
    Gene; 2005 Jan 03; 344():287-97. PubMed ID: 15656994
    [Abstract] [Full Text] [Related]

  • 12. Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency.
    Laumonnier F, Ronce N, Hamel BC, Thomas P, Lespinasse J, Raynaud M, Paringaux C, Van Bokhoven H, Kalscheuer V, Fryns JP, Chelly J, Moraine C, Briault S.
    Am J Hum Genet; 2002 Dec 03; 71(6):1450-5. PubMed ID: 12428212
    [Abstract] [Full Text] [Related]

  • 13. SOX3 is required during the formation of the hypothalamo-pituitary axis.
    Rizzoti K, Brunelli S, Carmignac D, Thomas PQ, Robinson IC, Lovell-Badge R.
    Nat Genet; 2004 Mar 03; 36(3):247-55. PubMed ID: 14981518
    [Abstract] [Full Text] [Related]

  • 14. Congenital hypopituitarism in two brothers with a duplication of the 'acrogigantism gene' GPR101: clinical findings and review of the literature.
    Elizabeth MSM, Verkerk AJMH, Hokken-Koelega ACS, Verlouw JAM, Argente J, Pfaeffle R, Neggers SJCMM, Visser JA, de Graaff LCG.
    Pituitary; 2021 Apr 03; 24(2):229-241. PubMed ID: 33184694
    [Abstract] [Full Text] [Related]

  • 15. The oncogenic potential of the high mobility group box protein Sox3.
    Xia Y, Papalopulu N, Vogt PK, Li J.
    Cancer Res; 2000 Nov 15; 60(22):6303-6. PubMed ID: 11103788
    [Abstract] [Full Text] [Related]

  • 16. A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation.
    Caburet S, Demarez A, Moumné L, Fellous M, De Baere E, Veitia RA.
    J Med Genet; 2004 Dec 15; 41(12):932-6. PubMed ID: 15591279
    [Abstract] [Full Text] [Related]

  • 17. PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expression.
    Klein AF, Ebihara M, Alexander C, Dicaire MJ, Sasseville AM, Langelier Y, Rouleau GA, Brais B.
    Exp Cell Res; 2008 May 01; 314(8):1652-66. PubMed ID: 18367172
    [Abstract] [Full Text] [Related]

  • 18. Sox3 regulates both neural fate and differentiation in the zebrafish ectoderm.
    Dee CT, Hirst CS, Shih YH, Tripathi VB, Patient RK, Scotting PJ.
    Dev Biol; 2008 Aug 01; 320(1):289-301. PubMed ID: 18572157
    [Abstract] [Full Text] [Related]

  • 19. The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.
    Kelberman D, Dattani MT.
    Ann Med; 2006 Aug 01; 38(8):560-77. PubMed ID: 17438671
    [Abstract] [Full Text] [Related]

  • 20. Sox3 expression identifies neural progenitors in persistent neonatal and adult mouse forebrain germinative zones.
    Wang TW, Stromberg GP, Whitney JT, Brower NW, Klymkowsky MW, Parent JM.
    J Comp Neurol; 2006 Jul 01; 497(1):88-100. PubMed ID: 16680766
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.