Genetic Variants of the <i>PLCXD3</i> Gene Are Associated with Risk of Metabolic Syndrome in the Emirati Population.

Aljaibeji, Hayat; Mohammed, Abdul Khader; Alkayyali, Sami; Hachim, Mahmood Yaseen; Hasswan, Hind; El-Huneidi, Waseem; Taneera, Jalal; Sulaiman, Nabil

Genetic Variants of the PLCXD3 Gene Are Associated with Risk of Metabolic Syndrome in the Emirati Population.

Aljaibeji, Hayat; Mohammed, Abdul Khader; Alkayyali, Sami; Hachim, Mahmood Yaseen; Hasswan, Hind; El-Huneidi, Waseem; Taneera, Jalal; Sulaiman, Nabil.

Afiliação

Aljaibeji H; Sharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAE.
Mohammed AK; Sharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAE.
Alkayyali S; Laboratory of Clinical Chemistry and Transfusion Medicine, Central Hospital of Växjö, Växjö 35188, Sweden.
Hachim MY; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai 505055, UAE.
Hasswan H; Sharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAE.
El-Huneidi W; Department of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah 27272, UAE.
Taneera J; Sharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAE.
Sulaiman N; Department of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah 27272, UAE.

Genes (Basel) ; 11(6)2020 06 18.

Article em En | MEDLINE | ID: mdl-32570874

Assuntos

Diabetes Mellitus Tipo 2/genética; Predisposição Genética para Doença; Genética Populacional; Síndrome Metabólica/genética; Fosfoinositídeo Fosfolipase C/genética; Adulto; Alelos; Índice de Massa Corporal; Diabetes Mellitus Tipo 2/patologia; Feminino; Estudos de Associação Genética; Genótipo; Hemoglobinas Glicadas/genética; Humanos; Masculino; Síndrome Metabólica/patologia; Pessoa de Meia-Idade; Polimorfismo de Nucleotídeo Único/genética; Fatores de Risco

Palavras-chave

BMI; CJD; HbA1c; LDL; MAF; MetS; SBP; body mass index; diastolic blood pressure; metabolic syndrome; minor allele frequency; phosphatidylinositol-specific phospholipase C X domain; single-nucleotide polymorphism; triglycerides; type 2 diabetes

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Síndrome Metabólica / Diabetes Mellitus Tipo 2 / Fosfoinositídeo Fosfolipase C / Genética Populacional Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

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