IPF 2008 Ⅰ

نویسندگان

چکیده

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Taking the "I" out of IPF.

As the authors describe, the initial evidence that pulmonary fibrosis may have a genetic basis emerged from case reports and case series that reported multiple cases of idiopathic interstitial pneumonias (IIPs) clustering in families [2–6]. The epidemiology indicates that within families containing two or more cases of IIP (familial interstitial pneumonia) the development of familial interstiti...

متن کامل

Sociologija i prostor 2008-2.indb

The paper presents the results of a survey carried out in the Slavonian village of Vođinci in 2006. The survey focused on the young people’s opinion about the quality of life and disadvantages of living in a rural area, and on their intention to stay in or leave the village. The results indicate that the main drawbacks for the young living in the village are poor working conditions (including u...

متن کامل

IPF: An Incremental Parallel Formulator

A computer simulation model of the human speaker is presented which generates sentences in a piecemeal way. The module responsible for Grammatical Encoding (the tactical component) is discussed in detail. Generation is conceptually and lexically guided and may proceed from the bottom of the syntactic structure upwards as well as from the top downwards. The construction of syntactic structures i...

متن کامل

Recommendations on treatment for IPF

Patient management in Idiopathic Pulmonary Fibrosis (IPF) is largely based on societal guidelines and recommendations. A recent update by the American Thoracic Society (ATS), European Respiratory Society (ERS), Japanese Respiratory Society (JRS) and Latin American Thoracic Association (ALAT) provided updated guidance on the diagnosis and management of IPF, along with recommendations on pharmaco...

متن کامل

MicroRNA-96 inhibits FoxO3a function in IPF fibroblasts on type I collagen matrix.

Idiopathic pulmonary fibrosis (IPF) is a lethal and progressive lung disease characterized by persistent (myo)fibroblasts and the relentless accumulation of collagen matrix. Unlike normal lung fibroblasts, IPF lung fibroblasts have suppressed forkhead box O3a (FoxO3a) activity, which allows them to expand in this diseased environment. microRNA-96 (miR-96) has recently been found to directly bin...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Seikei-Kakou

سال: 2009

ISSN: 0915-4027,1883-7417

DOI: 10.4325/seikeikakou.21.86