نتایج جستجو برای: pantothenate kinase

تعداد نتایج: 227686  

Journal: :Eukaryotic cell 2004
Jürgen Stolz Thomas Caspari Antony M Carr Norbert Sauer

The liz1+ gene of the fission yeast Schizosaccharomyces pombe was previously identified by complementation of a mutation that causes abnormal mitosis when ribonucleotide reductase is inhibited. Liz1 has similarity to transport proteins from Saccharomyces cerevisiae, but the potential substrate and its connection to the cell division cycle remain elusive. We report here that liz1+ encodes a plas...

Journal: :Neurology 2005
M T Pellecchia E M Valente L Cif S Salvi A Albanese V Scarano U Bonuccelli A R Bentivoglio A D'Amico C Marelli A Di Giorgio P Coubes P Barone B Dallapiccola

Pantothenate kinase-associated neurodegeneration (PKAN) is a rare autosomal-recessive disorder caused by mutations in the PANK2 gene. The authors report clinical and genetic findings of 16 patients with PKAN. The authors identified 12 mutations in the PANK2 gene, five of which were new. Only nine patients could be classified as classic or atypical PKAN, and intermediate phenotypes are described...

Pantothenate kinase- associated neurodegeneration (PKAN) syndrome is a rare autosomal recessive disorder characterized by progressive extrapyramidal dysfunction and iron accumulation in the brain and axonal spheroids in the central nervous system. It has been shown that the disorder is caused by mutations in PANK2 gene which codes for a mitochondrial enzyme participating in coenzyme A biosynthe...

2016
Raquel Quimas Molina da Costa Rogério Paysano Marrocos Marco Antonio Araujo Leite Fabio Henrique Gobbi Porto

The atypical form of Pantothenate Kinase-Associated Neurodegeneration (PKAN) tends to present at around the age of 14 years, has a heterogeneous presentation with extrapyramidal symptoms, and approximately one third of patients exhibit psychiatric problems. This paper reports the case of a patient with apparent typical symptoms of Tourette syndrome. However, the severity and poor response to tr...

2009
Muhammad Yousaf Raghu H. Ramakrishnaiah Chhavi Kaushik Manoj Kumar Chetan Chandulal Shah

Pantothenate kinase 2 deficiency (previously known as Hallervorden-Spatz disease) is an unusual metabolic disorder characterized by progressive extrapyramidal dysfunction and dementia. A 27-year-old Caucasian presented with a major depression disorder and social phobia since adolescence. Patient had marked paranoia, auditory hallucinations, extrapyramidal dysfunction, poor memory, and gait abno...

Journal: :Applied and environmental microbiology 1999
H Sahm L Eggeling

D-Pantothenate is synthesized via four enzymes from ketoisovalerate, which is an intermediate of branched-chain amino acid synthesis. We quantified three of these enzyme activities in Corynebacterium glutamicum and determined specific activities ranging from 0.00014 to 0.001 micromol/min mg (protein)-1. The genes encoding the ketopantoatehydroxymethyl transferase and the pantothenate synthetase...

2015
Diana C.F. Monteiro Vijay Patel Christopher P. Bartlett Shingo Nozaki Thomas D. Grant James A. Gowdy Gary S. Thompson Arnout P. Kalverda Edward H. Snell Hironori Niki Arwen R. Pearson Michael E. Webb

Coenzyme A (CoA) is an ubiquitous and essential cofactor, synthesized from the precursor pantothenate. Vitamin biosynthetic pathways are normally tightly regulated, including the pathway from pantothenate to CoA. However, no regulation of pantothenate biosynthesis has been identified. We have recently described an additional component in the pantothenate biosynthetic pathway, PanZ, which promot...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید