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Molecular structures and functional exploration of NDA family genes respond tolerant to alkaline stress in Gossypium hirsutum L

Fan, Yapeng; Zhang, Yuexin; Rui, Cun; Zhang, Hong; Xu, Nan; Wang, Jing; Han, Mingge; Lu, Xuke; Chen, Xiugui; Wang, Delong; Wang, Shuai; Guo, Lixue; Zhao, Lanjie; Huang, Hui; Wang, Junjuan; Sun, Liangqing; Chen, Chao; Ye, Wuwei.
Biol. Res; 55 (), 2022
BACKGROUND: The internal NAD(P)H dehydrogenase (NDA) gene family was a member of the NAD(P)H dehydrogenase (ND) gene family, mainly involved in the non-phosphorylated respiratory pathways in mitochondria and played crucial roles in response to abiotic stress. METHODS: The whole genome identification, str...
Regulación de la Expresión Génica de las Plantas, Gossypium/genética, Familia de Multigenes/genética, Proteínas de Plantas/genética, Proteínas de Plantas/metabolismo, Estrés Fisiológico/genética, Genoma de Planta, Estructura Molecular, Filogenia
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Genome-wide identification and characteristic analysis of the downstream melatonin metabolism gene GhM2H in Gossypium hirsutum L

Zhang, Yuexin; Wang, Jing; Chen, Xiugui; Lu, Xuke; Wang, Delong; Wang, Junjuan; Wang, Shuai; Chen, Chao; Guo, Lixue; Malik, Waqar Afzal; Fan, Yapeng; Rui, Cun; Cui, Ruifeng; Wang, Qinqin; Lei, Yuqian; Ye, Wuwei.
Biol. Res; 54 (), 2021
BACKGROUND: Melatonin 2-hydroxylase (M2H) is the first enzyme in the catabolism pathway of melatonin, which catalyzes the production of 2-hydroxymelatonin (2-OHM) from melatonin. The content of 2-hydroxymelatonin in plants is much higher than that of melatonin. So M2H may be a key enzyme in the metabolic...
Gossypium/genética, Melatonina, Regulación de la Expresión Génica de las Plantas, Proteínas de Plantas/genética, Proteínas de Plantas/metabolismo, Filogenia, Familia de Multigenes
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Regulación de expresión de genes de la familia de β-globina humana, útil en la búsqueda de nuevos blancos terapéuticos para tratamiento de hemoglobinopatías
Regulation of the β-globin gene family expression, useful in the search for new therapeutic targets for hemoglobinopathies

Scheps, Karen G; Varela, Viviana.
Medicina (B.Aires); 76 (6), 2016
Durante la etapa embrionaria, el desarrollo fetal y la vida posnatal se expresan isoformas funcionalmente distintas de hemoglobina, producto de la combinación de cadenas polipeptídicas sintetizadas a partir de los distintos genes que componen las familias de α- y β-globina. En función de que...
Regulación de la Expresión Génica, Expresión Génica, Hemoglobinopatías/genética, Hemoglobinopatías/terapia, Región de Control de Posición, Familia de Multigenes/genética, Globinas alfa/genética, Globinas beta/genética
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Uncommon allele in APO AI-CIII-AIV gene cluster in a family with congenital generalized lipodystrophy

Novak, Estela Maria; Longui, Carlos Alberto; Bydlowski, Sergio Paulo.
Säo Paulo med. j; 115 (6), 1997
Congenital generalized lipodystrophy is a rare inherited disease. One of its features is a disturbance in lipid metabolism characterized by hypercholesterolemia and hypertriglyceridemia. A brother and a sister with congenital generalized lipodystrophy, an 8-year old male and a 12-year old female were stu...
Alelos, Apolipoproteínas/genética, Familia de Multigenes/genética, Lipodistrofia/congénito, Lipodistrofia/genética, Triglicéridos/sangre, Polimorfismo Genético
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