نتایج جستجو برای: pank2 gene

تعداد نتایج: 1141396  

Journal: :American journal of nephrology 2013
Kyongtae T Bae Cheng Tao Jinhong Wang Diana Kaya Zhiyuan Wu Junu T Bae Arlene B Chapman Vicente E Torres Jared J Grantham Michal Mrug William M Bennett Michael F Flessner Doug P Landsittel

OBJECTIVE To evaluate whether kidney and cyst volumes can be accurately estimated based on limited area measurements from magnetic resonance (MR) images of patients with autosomal dominant polycystic kidney disease (ADPKD). MATERIALS AND METHODS MR coronal images of 178 ADPKD participants from the Consortium for Radiologic Imaging Studies of ADPKD (CRISP) were analyzed. For each MR image slic...

2016
Daniel Nassif João Santos Pereira Mariana Spitz Cláudia Capitão Alessandra Faria

Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive disorder caused by mutation in the PANK2 gene. It is characterized by abnormal brain iron accumulation, mainly in the globus pallidus. PKAN is included in a group of disorders known as neurodegeneration with brain iron accumulation (NBIA). We report a case of atypical PKAN with its most characteristic presentation...

Journal: :Movement disorders : official journal of the Movement Disorder Society 2009
Susanne A Schneider Kailash P Bhatia John Hardy

In addition to pure PD and pure dystonic syndromes, there are a group of disorders with overlapping features. The differential diagnosis of these dystonia parkinsonism syndromes can be complex. In view of the growing list of recognized disorders and recent advances in genetics, we review the autosomal recessive forms of dystonia parkinsonism, summarizing clinical presentations, results of inves...

Journal: :Human molecular genetics 2003
Konstanze Hörtnagel Holger Prokisch Thomas Meitinger

Mutations in the human PANK2 gene have been shown to occur in autosomal-recessive pantothenate kinase-associated neurodegeneration, a syndrome originally described by Hallervorden and Spatz. The kinase catalyses the first and rate-limiting step in the biosynthesis of coenzyme A, a key molecule in energy metabolism. We have determined the exon-intron structure of the hPANK2 gene and identified t...

2016
Daniel I Orellana Paolo Santambrogio Alicia Rubio Latefa Yekhlef Cinzia Cancellieri Sabrina Dusi Serena G Giannelli Paola Venco Pietro G Mazzara Anna Cozzi Maurizio Ferrari Barbara Garavaglia Stefano Taverna Valeria Tiranti Vania Broccoli Sonia Levi

Pantothenate kinase-associated neurodegeneration (PKAN) is an early onset and severely disabling neurodegenerative disease for which no therapy is available. PKAN is caused by mutations in PANK2, which encodes for the mitochondrial enzyme pantothenate kinase 2. Its function is to catalyze the first limiting step of Coenzyme A (CoA) biosynthesis. We generated induced pluripotent stem cells from ...

2016
Robert J. Hart Emmanuel Cornillot Amanah Abraham Emily Molina Catherine S. Nation Choukri Ben Mamoun Ahmed S. I. Aly

The metabolic machinery for the biosynthesis of Coenzyme A (CoA) from exogenous pantothenic acid (Vitamin B5) has long been considered as an excellent target for the development of selective antimicrobials. Earlier studies in the human malaria parasite Plasmodium falciparum have shown that pantothenate analogs interfere with pantothenate phosphorylation and block asexual blood stage development...

2017
Charles Arber Plamena R Angelova Sarah Wiethoff Yugo Tsuchiya Francesca Mazzacuva Elisavet Preza Kailash P Bhatia Kevin Mills Ivan Gout Andrey Y Abramov John Hardy James A Duce Henry Houlden Selina Wray

Mutations in PANK2 lead to neurodegeneration with brain iron accumulation. PANK2 has a role in the biosynthesis of coenzyme A (CoA) from dietary vitamin B5, but the neuropathological mechanism and reasons for iron accumulation remain unknown. In this study, atypical patient-derived fibroblasts were reprogrammed into induced pluripotent stem cells (iPSCs) and subsequently differentiated into cor...

Journal: :Journal of medical genetics 2009
A Gregory B J Polster S J Hayflick

Neurodegeneration with brain iron accumulation (NBIA) describes a group of progressive neurodegenerative disorders characterised by high brain iron and the presence of axonal spheroids, usually limited to the central nervous system. Mutations in the PANK2 gene account for the majority of NBIA cases and cause an autosomal recessive inborn error of coenzyme A metabolism called pantothenate kinase...

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