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

436 related items for PubMed ID: 11406664

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

  • 2. Mutation analysis of the TSC1 and TSC2 genes in Japanese patients with pulmonary lymphangioleiomyomatosis.
    Sato T, Seyama K, Fujii H, Maruyama H, Setoguchi Y, Iwakami S, Fukuchi Y, Hino O.
    J Hum Genet; 2002; 47(1):20-8. PubMed ID: 11829138
    [Abstract] [Full Text] [Related]

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

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 7. A calmodulin binding site in the tuberous sclerosis 2 gene product is essential for regulation of transcription events and is altered by mutations linked to tuberous sclerosis and lymphangioleiomyomatosis.
    Noonan DJ, Lou D, Griffith N, Vanaman TC.
    Arch Biochem Biophys; 2002 Feb 01; 398(1):132-40. PubMed ID: 11811958
    [Abstract] [Full Text] [Related]

  • 8. The spectrum of mutations in TSC1 and TSC2 in women with tuberous sclerosis and lymphangiomyomatosis.
    Strizheva GD, Carsillo T, Kruger WD, Sullivan EJ, Ryu JH, Henske EP.
    Am J Respir Crit Care Med; 2001 Jan 01; 163(1):253-8. PubMed ID: 11208653
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex.
    Sancak O, Nellist M, Goedbloed M, Elfferich P, Wouters C, Maat-Kievit A, Zonnenberg B, Verhoef S, Halley D, van den Ouweland A.
    Eur J Hum Genet; 2005 Jun 01; 13(6):731-41. PubMed ID: 15798777
    [Abstract] [Full Text] [Related]

  • 11. Lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia, and clear-cell micronodules in a 39-year-old woman with tuberous sclerosis: a case report.
    Chang MH, Yao-Peng H.
    Int J Surg Pathol; 2010 Dec 01; 18(6):522-5. PubMed ID: 20667922
    [Abstract] [Full Text] [Related]

  • 12. Mutation and polymorphism analysis of TSC1 and TSC2 genes in Indian patients with tuberous sclerosis complex.
    Ali M, Girimaji SC, Markandaya M, Shukla AK, Sacchidanand S, Kumar A.
    Acta Neurol Scand; 2005 Jan 01; 111(1):54-63. PubMed ID: 15595939
    [Abstract] [Full Text] [Related]

  • 13. Analysis of all exons of TSC1 and TSC2 genes for germline mutations in Japanese patients with tuberous sclerosis: report of 10 mutations.
    Yamashita Y, Ono J, Okada S, Wataya-Kaneda M, Yoshikawa K, Nishizawa M, Hirayama Y, Kobayashi E, Seyama K, Hino O.
    Am J Med Genet; 2000 Jan 17; 90(2):123-6. PubMed ID: 10607950
    [Abstract] [Full Text] [Related]

  • 14. Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis.
    Niida Y, Lawrence-Smith N, Banwell A, Hammer E, Lewis J, Beauchamp RL, Sims K, Ramesh V, Ozelius L.
    Hum Mutat; 1999 Jan 17; 14(5):412-22. PubMed ID: 10533067
    [Abstract] [Full Text] [Related]

  • 15. Pulmonary lymphangioleiomyomatosis in a man.
    Aubry MC, Myers JL, Ryu JH, Henske EP, Logginidou H, Jalal SM, Tazelaar HD.
    Am J Respir Crit Care Med; 2000 Aug 17; 162(2 Pt 1):749-52. PubMed ID: 10934115
    [Abstract] [Full Text] [Related]

  • 16. Mutational analysis of the tuberous sclerosis gene TSC2 in patients with pulmonary lymphangioleiomyomatosis.
    Astrinidis A, Khare L, Carsillo T, Smolarek T, Au KS, Northrup H, Henske EP.
    J Med Genet; 2000 Jan 17; 37(1):55-7. PubMed ID: 10633137
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Mutational and radiographic analysis of pulmonary disease consistent with lymphangioleiomyomatosis and micronodular pneumocyte hyperplasia in women with tuberous sclerosis.
    Franz DN, Brody A, Meyer C, Leonard J, Chuck G, Dabora S, Sethuraman G, Colby TV, Kwiatkowski DJ, McCormack FX.
    Am J Respir Crit Care Med; 2001 Aug 15; 164(4):661-8. PubMed ID: 11520734
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects.
    Mayer K, Ballhausen W, Rott HD.
    Hum Mutat; 1999 Aug 15; 14(5):401-11. PubMed ID: 10533066
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 22.