نتایج جستجو برای: hadh

تعداد نتایج: 56  

2017
Congcong Shen Yao-Hua Song Yufeng Xie Xiaoxiao Wang Yunliang Wang Chao Wang Songbai Liu Sheng-Li Xue Yangxin Li Bin Liu Zaixiang Tang Weichang Chen Jenny Song Hesham M. Amin Jin Zhou

HADH is a key enzyme in fatty acid oxidation. The aim of this study was to identify the role of HADH in gastric cancer. We analyzed the expression of HADH in 102 pairs of gastric cancer samples. Western blot analysis revealed that HADH was decreased in stage I/II gastric cancer samples compared to matched adjacent normal gastric tissue, and its expression was further decreased in stage III/IV s...

2012
Amanda J Heslegrave Ritika R Kapoor Simon Eaton Bernadette Chadefaux Teoman Akcay Enver Simsek Sarah E Flanagan Sian Ellard Khalid Hussain

BACKGROUND Loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase (HADH) cause protein sensitive hyperinsulinaemic hypoglycaemia (HH). HADH encodes short chain 3-hydroxacyl-CoA dehydrogenase, an enzyme that catalyses the penultimate reaction in mitochondrial β-oxidation of fatty acids. Mutations in GLUD1 encoding glutamate dehydrogenase, also cause protein sensitive HH (due to leucine se...

Journal: :The Journal of biological chemistry 2010
Changhong Li Pan Chen Andrew Palladino Srinivas Narayan Laurie K Russell Samir Sayed Guoxiang Xiong Jie Chen David Stokes Yasmeen M Butt Patricia M Jones Heather W Collins Noam A Cohen Akiva S Cohen Itzhak Nissim Thomas J Smith Arnold W Strauss Franz M Matschinsky Michael J Bennett Charles A Stanley

The mechanism of insulin dysregulation in children with hyperinsulinism associated with inactivating mutations of short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) was examined in mice with a knock-out of the hadh gene (hadh(-/-)). The hadh(-/-) mice had reduced levels of plasma glucose and elevated plasma insulin levels, similar to children with SCHAD deficiency. hadh(-/-) mice were hypersen...

Journal: :Acta crystallographica. Section F, Structural biology and crystallization communications 2008
Timothy M Reed Hidehiko Hirakawa Minae Mure Emily E Scott Julian Limburg

Histamine dehydrogenase (HADH) from Nocardioides simplex catalyzes the oxidative deamination of histamine to produce imidazole acetaldehyde and an ammonium ion. HADH is functionally related to trimethylamine dehydrogenase (TMADH), but HADH has strict substrate specificity towards histamine. HADH is a homodimer, with each 76 kDa subunit containing two redox cofactors: a [4Fe-4S] cluster and an u...

2011
Nadja Schulz Heinz Himmelbauer Michaela Rath Michel van Weeghel Sander Houten Wim Kulik Karsten Suhre Stephan Scherneck Heike Vogel Reinhart Kluge Petra Wiedmer Hans-Georg Joost Annette Schürmann

Dysregulation of fatty acid oxidation plays a pivotal role in the pathophysiology of obesity and insulin resistance. Medium- and short-chain-3-hydroxyacyl-coenzyme A (CoA) dehydrogenase (SCHAD) (gene name, hadh) catalyze the third reaction of the mitochondrial β-oxidation cascade, the oxidation of 3-hydroxyacyl-CoA to 3-ketoacyl-CoA, for medium- and short-chain fatty acids. We identified hadh a...

Journal: :Memorias do Instituto Oswaldo Cruz 2004
Miguel A Chena Silvia Elizondo-Jiménez Lorena Rodríguez-Páez Benjamín Nogueda-Torres Isabel Baeza-Ramírez Carlos Wong-Ramírez

N-allyl (NAOx) and N-propyl (NPOx) oxamates were designed as inhibitors of alpha-hydroxyacid dehydrogenase (HADH) isozyme II from Trypanosoma cruzi. The kinetic studies showed that NAOx and NPOx were competitive inhibitors of HADH-isozyme II (Ki = 72 microM, IC50 = 0.33 mM and 70 microM, IC50 = 0.32 mM, respectively). The attachment of the allylic and propylic chains to nitrogen of the competit...

Journal: :Indian pediatrics 2016
Amit Kumar Satapathy Vandana Jain Sian Ellard Sarah E Flanagan

BACKGROUND Hyperinsulinemia is the commonest cause of persistent hypoglycemia in infancy. Inactivating mutations in the genes ABCC8 and KCNJ11 are the commonest cause. Mutation in the HADH gene, which encodes the short-chain-L-3-hydroxyacyl-CoA dehydrogenase, is a rare cause. CASE CHARACTERISTICS Two Indian sisters who presented with hyperinsulinemic hypoglycemia of infancy. OBSERVATION/INT...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2001
R H Lane D E Kelley E M Gruetzmacher S U Devaskar

Multiple adult morbidities are associated with intrauterine growth retardation (IUGR) including dyslipidemia. We hypothesized that uteroplacental insufficiency and subsequent IUGR in the rat would lead to altered hepatic fatty acid metabolism. To test this hypothesis, we quantified hepatic mRNA levels of acetyl-CoA carboxylase (ACC), carnitine palmitoyltransferase (CPTI), the beta-oxidation-tri...

2015
Emine Çamtosun Sarah E. Flanagan Sian Ellard Zeynep Şıklar Khalid Hussain Pınar Kocaay Merih Berberoğlu

Unlike other congenital fatty acid oxidation defects, short-chain L-3-hydroxyacyl-CoA (SCHAD, HADH) deficiency is characterised by hypoglycemia with hyperinsulinism in the neonatal or infancy periods. The long-term and detailed clinical progression of the disease is largely unknown with almost 40 patients reported and only a few patients described clinically. We present clinical and laboratory ...

2013
Ritika R Kapoor Sarah E Flanagan Ved Bhushan Arya Julian P Shield Sian Ellard Khalid Hussain

BACKGROUND Congenital hyperinsulinism (CHI) is a clinically heterogeneous condition. Mutations in eight genes (ABCC8, KCNJ11, GLUD1, GCK, HADH, SLC16A1, HNF4A and HNF1A) are known to cause CHI. AIM To characterise the clinical and molecular aspects of a large cohort of patients with CHI. METHODOLOGY Three hundred patients were recruited and clinical information was collected before genotypi...

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