Browsing Departamento de Biología Celular by Author "Kaminski, N"

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Browsing Departamento de Biología Celular by Author "Kaminski, N"

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  • Zuo, FR; Kaminski, N; Eugui, E; Allard, J; Yakhini, Z; Ben-Dor, A; Lollini, L; Morris, D; Kim, Y; DeLustro, B; Sheppard, D; Selman, M; Heller, RA; Pardo-Cemo, Annie (2002)
    Pulmonary fibrosis is a progressive and largely untreatable group of disorders that affects up to 100,000 people on any given day in the United States. To elucidate the molecular mechanisms that lead to end-stage human ...
  • Selman, M; Barrera, L; Estrada, A; Watson, SR; Wilson, K; Aziz, N; Kaminski, N; Zlotnik, A; Pardo-Cemo, Annie (2006)
    Rationale: Many of the interstitial lung diseases represent a diagnostic and therapeutic challenge because their clinical and even histologic features are often nonspecific. Likewise, the transcriptional signatures of most ...
  • Pandit, KV; Corcoran, D; Yousef, H; Yarlagadda, M; Tzouvelekis, A; Gibson, KF; Konishi, K; Yousem, SA; Singh, M; Handley, D; Richards, T; Selman, M; Watkins, SC; Ben-Yehudah, A; Bouros, D; Eickelberg, O; Ray, P; Benos, PV; Kaminski, N; Pardo-Cemo, Annie (2010)
    Rationale: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and usually lethal fibrotic lung disease characterized by profound changes in epithelial cell phenotype and fibroblast proliferation. Objectives. ...
  • Gibson, K; Cisneros, J; Richards, TJ; Yang, Y; Becerril, C; Yousem, S; Herrera, L; Ruiz, V; Selman, M; Kaminski, N; Pardo-Cemo, Annie (2005)
    Background Idiopathic pulmonary fibrosis (IPF) is a progressive and lethal disorder characterized by fibroproliferation and excessive accumulation of extracellular matrix in the lung. Methods and Findings Using oligonucleotide ...

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