نتایج جستجو برای: gne

تعداد نتایج: 282  

2013
Frank Hanisch Wenke Weidemann Mona Großmann Pushpa Raj Joshi Hans-Jürgen Holzhausen Gisela Stoltenburg Joachim Weis Stephan Zierz Rüdiger Horstkorte

Sialic acids (Sia) are widely expressed as terminal monosaccharides on eukaryotic glycoconjugates. They are involved in many cellular functions, such as cell-cell interaction and signal recognition. The key enzyme of sialic acid biosynthesis is the bifunctional UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (GNE), which catalyses the first two steps of Sia biosynthesis in the cy...

Journal: :Pathobiology : journal of immunopathology, molecular and cellular biology 2010
Kenichiro Nakamura Yoshiyuki Tsukamoto Naoki Hijiya Yasunori Higuchi Shinji Yano Shigeo Yokoyama Toshihide Kumamoto Masatsugu Moriyama

OBJECTIVE The aim of the present study was to clarify the expression of uridine diphospho-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) protein and mRNA in damaged or regenerating myofibers. METHODS We investigated the muscle expression pattern of GNE protein by immunohistochemistry using a murine model involving intramuscular injection of cardiotoxin (CTX), and the express...

2009
Anagha P. Phadke Chris Jay Salina J. Chen Courtney Haddock Zhaohui Wang Yang Yu Derek Nemunaitis Gregory Nemunaitis Nancy S. Templeton Neil Senzer Phillip B. Maples Alex W. Tong John Nemunaitis

Hereditary inclusion body myopathy-2 (HIBM2) is an adult-onset, muscular disease caused by mutations in the GNE gene. HIBM2-associated GNE mutations causing hyposialyation have been proposed to contribute to reduced muscle function in patients with HIBM2, though the exact cause of this disease is unknown. In the current studies we examined pre-clinical in vivo toxicity, and expression of the pl...

2013
Jae Eun Sim Ji-Man Hong Gyoung Im Suh Hanna Cho Kyung Seok Park Eun-Hee Sohn Young-Chul Choi

BACKGROUND GNE myopathy is characterized by early-adult-onset distal myopathy sparing quadriceps caused by mutations in the GNE gene encoding UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, an enzyme in the sialic-acid synthesis pathway. CASE REPORT A 27-year-old Korean woman presented a rapid deterioration in strength of the distal lower limbs during her first pregnancy. She ...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2013
Xingrong Liu Harvey Wong Kimberly Scearce-Levie Ryan J Watts Melis Coraggio Young G Shin Kun Peng Kristin R Wildsmith Jasvinder K Atwal Jason Mango Stephen P Schauer Kelly Regal Kevin W Hunt Allen A Thomas Michael Siu Joseph Lyssikatos Gauri Deshmukh Cornelis E C A Hop

This study was conducted to determine the pharmacokinetics (PK) and pharmacodynamics (PD) of two novel inhibitors of β-site amyloid precursor protein (APP)-cleaving enzyme (BACE1), GNE-629 [(4S,4a'S,10a'S)-2-amino-8'-(2-fluoropyridin-3-yl)-1-methyl-3',4',4a',10a'-tetrahydro-1'H-spiro[imidazole-4,10'-pyrano[4,3-b]chromen]-5(1H)-one] and GNE-892 [(R)-2-amino-1,3',3'-trimethyl-7'-(pyrimidin-5-yl)-...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2014
Amina Chaouch Kathryn M Brennan Judith Hudson Cheryl Longman John McConville Patrick J Morrison Maria E Farrugia Richard Petty Willie Stewart Fiona Norwood Rita Horvath Patrick F Chinnery Donald Costigan John Winer Tuomo Polvikoski Estelle Healy Anna Sarkozy Teresinha Evangelista Oksana Pogoryelova Michelle Eagle Kate Bushby Volker Straub Hanns Lochmüller

OBJECTIVE GNE myopathy is a rare recessive myopathy associated with inclusion bodies on muscle biopsy. The clinical phenotype is associated with distal muscle weakness with quadriceps sparing. Most of the current information on GNE myopathy has been obtained through studies of Jewish and Japanese patient cohorts carrying founder mutations in the GNE gene. However, little is known about GNE myop...

Journal: :Automatica 2012
Ankur A. Kulkarni Uday V. Shanbhag

We are concerned with a class of Nash games in which the players’ strategy sets are coupled by a shared constraint. A widely employed solution concept for such games, referred to as generalized Nash games, is the generalized Nash equilibrium (GNE). The variational equilibrium (VE) [6] is a specific kind of GNE given by a solution of the variational inequality formed from the common constraint a...

Journal: :The journal of gene medicine 2010
Gregory Nemunaitis Phillip B Maples Chris Jay William A Gahl Marjan Huizing Justin Poling Alex W Tong Anagha P Phadke Beena O Pappen Cynthia Bedell Nancy S Templeton Joseph Kuhn Neil Senzer John Nemunaitis

BACKGROUND Hereditary inclusion body myopathy (HIBM) is an autosomal recessive adult onset myopathy. It is characterized by mutations of the GNE (UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase) gene. Afflicted patients have no therapeutic options. In preclinical testing, we have previously demonstrated the ability to correct GNE gene function and the safety of delivery of wild t...

2013
Jae Eun Sim Hyung-Jun Park Ha Young Shin Tai-Seung Nam Seung Min Kim Young-Chul Choi

PURPOSE Glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase (GNE) myopathy is an autosomal recessive neuromuscular disorder characterized by early adult-onset weakness of the distal muscles of the lower limbs. The clinical spectrum of GNE myopathy varies, and it is not clear how the same GNE gene mutations can result in different phenotypes. Here, we present clinical, pathological...

Journal: :Neuropharmacology 2017
Tzu-Ming Wang Brandon M. Brown Lunbin Deng Benjamin D. Sellers Patrick J. Lupardus Heidi J.A. Wallweber Amy Gustafson Evera Wong Matthew Volgraf Jacob B. Schwarz David H. Hackos Jesse E. Hanson

Ionotropic glutamate receptors (iGluRs) mediate fast excitatory neurotransmission and are key nervous system drug targets. While diverse pharmacological tools have yielded insight into iGluR extracellular domain function, less is known about molecular mechanisms underlying the ion conduction gating process within the transmembrane domain (TMD). We have discovered a novel NMDAR positive alloster...

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