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British Journal of Dermatology, ISSN 0007-0963, 08/2019, Volume 181, Issue 2, pp. 241 - 241
Linked Article: Zhu et al. Br J Dermatol 2019; 181:304–313. 
MISSENSE MUTATION | ONE CHINESE FAMILY | MVK GENE | DERMATOLOGY
Journal Article
Journal of Environmental Sciences, ISSN 1001-0742, 09/2019
Journal Article
Applied Catalysis B: Environmental, ISSN 0926-3373, 08/2004, Volume 51, Issue 4, pp. 229 - 238
The kinetics of the oxidation of methane over a commercial 0.5% Pd on γ-Al O catalyst has been studied in a lab-scale fixed-bed reactor, the effect of... 
MVK mechanism | Kinetics | Methane oxidation | Steam inhibition
Journal Article
BioResources, 02/2011, Volume 6, Issue 1, pp. 686 - 699
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 08/2006, Volume 27, Issue 8, pp. 796 - 802
Mevalonate kinase deficiency (MKD) is an autosomal recessive autoinflammatory disorder caused by mutations in the MVK gene resulting in deficient activity of... 
MVK | SYNDROME HIDS | PERIODIC FEVER SYNDROME | IDENTIFICATION | mevalonate kinase deficiency | MOLECULAR ANALYSIS | HIDS | IN-VITRO | HYPER-IGD | ISOPRENOID BIOSYNTHESIS | ACIDURIA | GENETICS & HEREDITY | HYPERIMMUNOGLOBULINEMIA-D | MVK MUTATIONS | mevalonate kinase | periodic fever
Journal Article
by Zhu, T and Tian, D and Zhang, L and Xu, X and Xia, K and Hu, Z and Xiong, Z and Tan, J
British Journal of Dermatology, ISSN 0007-0963, 08/2019, Volume 181, Issue 2, pp. 304 - 313
Summary Background Disseminated superficial actinic porokeratosis (DSAP) is a rare autosomal dominant disease. In our previous research, we found that a... 
ONE CHINESE FAMILY | MVK GENE | APOPTOSIS | CELLS | PATHWAY | MISSENSE MUTATION | IDENTIFICATION | SIMVASTATIN | LOCUS | DERMATOLOGY | Medicine, Experimental | Medical research | Mevalonate kinase | Cycloheximide | Mitochondria | Mevalonic acid | Missense mutation | Pedigree | Mutation | Kinases | Dimerization | Cholesterol | Glutathione | Apoptosis
Journal Article
Pediatrics, ISSN 0031-4005, 07/2011, Volume 128, Issue 1, pp. e152 - e159
Journal Article
FRONTIERS IN IMMUNOLOGY, ISSN 1664-3224, 08/2019, Volume 10, p. 1900
The rare autoinflammatory disease mevalonate kinase deficiency (MKD, which includes HIDS and mevalonic aciduria) is caused by recessive, pathogenic variants in... 
Rab GTPase | GENOTYPE | autoinflammation | PHENOTYPE | IMMUNOLOGY | HIDS | HYPER-IGD | GENE | Rap1 | HYPERIMMUNOGLOBULINEMIA-D | prenylation | MVK MUTATIONS | mevalonate kinase | Proteins
Journal Article
Human mutation, ISSN 1059-7794, 2008, Volume 29, Issue 6, pp. 803 - 808
Infevers (Internet Fevers; http://fmf.igh.cnrs.fr/ISSAID/infevers), a website dedicated to mutations responsible for hereditary autoinflammatory diseases, was... 
registry | PSTPIP1 | MVK | NLRP7 | autoinflammatory disease | NLRP3 | NOD2 | Infevers | MEFV | LPIN2 | TNFRSF1A | Autoinflammatory disease | Registry | PROTEIN | infevers | DISORDERS | MULTIFOCAL OSTEOMYELITIS | PATHWAY | DISEASE | GENETICS & HEREDITY | MAJEED-SYNDROME | SYNDROME | ASSOCIATION | FEVER | User-Computer Interface | Confidentiality | Humans | Familial Mediterranean Fever - genetics | Databases, Genetic | Registries | Internet | Mutation
Journal Article
Journal of Hazardous Materials, ISSN 0304-3894, 09/2018, Volume 357, pp. 332 - 340
To achieve efficient degradation of toluene, a series of Cu Mn Ce O /sepiolite catalysts (  = 0.1, 0.2, and 0.3) with different Cu Mn Ce O loadings (10%, 20%,... 
Cu1-yMn2CeyOx/sepiolite | Toluene oxidation | CeO2-CuMn2O4 interaction | Structural characterization | MVK model | CuMn | interaction | sepiolite | CeO | MIXED OXIDES | CuO2-CuMn2O4 interaction | METAL-OXIDE | CU-MN | DIESEL SOOT | OXIDE CATALYSTS | LOW-TEMPERATURE | MANGANESE OXIDE | ENVIRONMENTAL SCIENCES | GAS SHIFT REACTION | ENGINEERING, ENVIRONMENTAL | CATALYTIC-OXIDATION | VOLATILE ORGANIC-COMPOUNDS
Journal Article
Journal of Modern Optics, ISSN 0950-0340, 07/2019, Volume 66, Issue 13, pp. 1392 - 1407
Anisoplanatic electromagnetic (EM) propagation across a turbulent atmosphere has been recently examined for an unmodulated carrier propagating over an... 
turbulent and chaotic propagation | acousto-optic chaos | MVK turbulence | anisoplanatic propagation | image encryption | BEAMS | LIGHT | DIFFRACTION | BRAGG | FORMALISM | OPTICS | Mitigation | Turbulence | Digital imaging | Turbulent flow | Propagation | Atmospheric models | Heterodyning | Signal reconstruction | Encryption | Security | Recovery | Demodulation
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 2016, Volume 68, Issue 11, pp. 2795 - 2805
Objective Mevalonate kinase deficiency (MKD) is a rare metabolic disease characterized by recurrent inflammatory episodes. This study was undertaken to... 
MVK | HYPER-IGD | PERIODIC FEVER SYNDROME | ACIDURIA | HYPERIMMUNOGLOBULINEMIA-D | AUTOINFLAMMATORY DISEASES | MUTATIONS | SPECTRUM | RHEUMATOLOGY | Arthralgia - etiology | Uveitis - etiology | Humans | Child, Preschool | Lymphadenopathy - etiology | Male | Arthralgia - physiopathology | Arthritis - genetics | Stomatitis, Aphthous - genetics | Cerebellar Diseases - physiopathology | Amyloidosis - genetics | Skin Diseases - physiopathology | Amyloidosis - etiology | Child | Stomatitis, Aphthous - etiology | Infant, Newborn | Myalgia - physiopathology | Amyloidosis - physiopathology | Genotype | Headache - physiopathology | Vomiting - genetics | Phenotype | Diarrhea - genetics | Abdominal Pain - genetics | Adolescent | Age of Onset | Intellectual Disability - etiology | Uveitis - genetics | Vomiting - physiopathology | Conjunctivitis - etiology | Conjunctivitis - genetics | Arthritis - physiopathology | Headache - etiology | Skin Diseases - genetics | Mevalonate Kinase Deficiency - physiopathology | Myalgia - genetics | Cerebellar Diseases - etiology | Diarrhea - physiopathology | Infant | Mevalonate Kinase Deficiency - genetics | Intellectual Disability - genetics | Pharyngitis - genetics | Arthritis - etiology | Female | Registries | Retrospective Studies | Arthralgia - genetics | Pharyngitis - physiopathology | Abdominal Pain - etiology | Pharyngitis - etiology | Lymphadenopathy - genetics | Abdominal Pain - physiopathology | Myalgia - etiology | Phosphotransferases (Alcohol Group Acceptor) - genetics | Headache - genetics | Intellectual Disability - physiopathology | Skin Diseases - etiology | Cerebellar Diseases - genetics | Conjunctivitis - physiopathology | Mevalonate Kinase Deficiency - complications | Stomatitis, Aphthous - physiopathology | Vomiting - etiology | Diarrhea - etiology | Lymphadenopathy - physiopathology | Uveitis - physiopathology | Kinases | Genotype & phenotype | Index Medicus | Abridged Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 1999, Volume 22, Issue 2, pp. 178 - 181
Hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS; MIM 260920) is a rare, apparently monogenic, autosomal recessive disorder characterized by... 
ATTACKS | FAMILIAL HIBERNIAN FEVER | CLINICAL SPECTRUM | ACIDURIA | GENETICS & HEREDITY | HYPERIMMUNOGLOBULINEMIA-D | 12P13 | IDENTIFICATION | LINKAGE | MVK gene | familial Mediterranean fever | periodic fever syndrome | hyperimmunoglobulinemia D | familial Hibernian fever | HIDS gene
Journal Article
Rheumatology International, ISSN 0172-8172, 1/2018, Volume 38, Issue 1, pp. 121 - 127
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease. Mutations in MVK gene are associated with MKD with modest genotype–phenotype... 
MVK | Genetic variability | Medicine & Public Health | MMAB | Rheumatology | Haplotype structure | Mevalonate kinase deficiency | FRAMEWORK | LOCI | RHEUMATOLOGY | ASSOCIATION | GENOME | Blood cholesterol | Genes | Analysis | Kinases | Mutation
Journal Article
Biological and Pharmaceutical Bulletin, ISSN 0918-6158, 2016, Volume 39, Issue 6, pp. 909 - 914
Cigarette mainstream smoke is composed of gas and tar phases and contains >4000 chemical constituents, including nicotine and tar. The substances in the gas... 
Journal Article
Journal of Volcanology and Geothermal Research, ISSN 0377-0273, 2008, Volume 174, Issue 1, pp. 57 - 67
Tuffisitic Kimberlite (TK) is a textural variety of kimberlite first described from a number of southern African kimberlite pipes. This particular variety of... 
Tuffisitic Kimberlite breccia, TKB | kimberlite emplacement | diatreme | Massive Volcaniclastic Kimberlite, MVK | Massive Volcaniclastic Kimberlite | GEOSCIENCES, MULTIDISCIPLINARY | MVK | GEOLOGY | Tuffisitic Minberlite breccia | DIAMOND | TKB | PIPES | Breccia | Diamond mining
Journal Article