نتایج جستجو برای: congenital hepatic fibrosis

تعداد نتایج: 311139  

Journal: :Human mutation 2009
Francesco Brancati Miriam Iannicelli Lorena Travaglini Annalisa Mazzotta Enrico Bertini Eugen Boltshauser Stefano D'Arrigo Francesco Emma Elisa Fazzi Romina Gallizzi Mattia Gentile Damir Loncarevic Vlatka Mejaski-Bosnjak Chiara Pantaleoni Luciana Rigoli Carmelo D Salpietro Sabrina Signorini Gilda Rita Stringini Alain Verloes Dominika Zabloka Bruno Dallapiccola Joseph G Gleeson Enza Maria Valente

The acronym COACH defines an autosomal recessive condition of Cerebellar vermis hypo/aplasia, Oligophrenia, congenital Ataxia, Coloboma and Hepatic fibrosis. Patients present the "molar tooth sign", a midbrain-hindbrain malformation pathognomonic for Joubert Syndrome (JS) and Related Disorders (JSRDs). The main feature of COACH is congenital hepatic fibrosis (CHF), resulting from malformation o...

Ahmad Vosough Dizaj Hamid Gourabi Iman Salahshourifar Mohamad Ali Sadighi Gilani Ramin Radpour,

A qualitative diagnosis of infertility requires attention to female and male physical abnormalities, endocrine anomalies and genetic conditions that interfere with reproduction. Many genes are likely to be involved in the complex process of reproduction. Cystic fibrosis (CF) incidence varies in different White people populations (a higher incidence of CF is observed in northern–western European...

Journal: :American journal of physiology. Renal physiology 2011
Daisuke Yoshihara Hiroki Kurahashi Miwa Morita Masanori Kugita Yoshiyuki Hiki Harold M Aukema Tamio Yamaguchi James P Calvet Darren P Wallace Shizuko Nagao

In autosomal recessive polycystic kidney disease (ARPKD), progressive enlargement of fluid-filled cysts is due to aberrant proliferation of tubule epithelial cells and transepithelial fluid secretion leading to extensive nephron loss and interstitial fibrosis. Congenital hepatic fibrosis associated with biliary cysts/dilatations is the most common extrarenal manifestation in ARPKD and can lead ...

Hong Mei Mi Hui Li Rong-Qi Wang Su Xian Zhao Yan Hong Jia Yue-Min Nan,

Objective(s):Fuzheng Huayu recipe (FZHY) exerts significant protective effects against liver fibrosis by strengthening the body’s resistance and removing blood stasis. However, the molecular mechanisms through which FZHY affects liver fibrosis are still unclear. In this study, we examined the expression levels of factors involved in the inhibitor κB kinase-β (IKK-β)/nuclear factor-κB (NF-κB) an...

Journal: :Comparative Hepatology 2004
Kazuhiko Besshi Mutsunori Fujiwara Haruki Senoo Yasufumi Kondou Yoshitaka Ohsugi Taiji Hayashi Kozo Ishidate

Introduction Quiescent hepatic stellate cells (HSCs) store vitamin A as lipid droplets in the cytoplasm. The activated HSCs by several stimuli have functions similar to that of myofibroblasts and play key roles in hepatic fibrosis [1-3]. However, precise timing between activation of the HSC and induction of hepatic fibrosis is still unknown. Cholinedeficient (CD) diet induces fatty liver and su...

2013
Hye Ran Yang

Because nonalcoholic steatohepatitis can progress towards cirrhosis even in children, early detection of hepatic fibrosis and accurate diagnosis of nonalcoholic fatty liver disease (NAFLD) are important. Although liver biopsy is regarded as the gold standard of diagnosis, its clinical application is somewhat limited in children due to its invasiveness. Noninvasive diagnostic methods, including ...

2017
Yukiomi Nakade Kazumasa Sakamoto Taeko Yamauchi Tadahisa Inoue Yuji Kobayashi Takaya Yamamoto Norimitsu Ishii Tomohiko Ohashi Yoshio Sumida Kiyoaki Ito Haruhisa Nakao Yoshitaka Fukuzawa Kazuo Umezawa Masashi Yoneda

Conophylline (CnP), a vinca alkaloid extracted from the leaves of the tropical plant Ervatamia microphylla, attenuates hepatic fibrosis in mice. However, little is known about whether CnP inhibits steatosis, inflammation, and fibrosis in non-alcoholic steatohepatitis (NASH) in mice. A methionine-choline-deficient (MCD) diet was administered to male db/db mice as a NASH model, and CnP (1 μg/kg/d...

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