Search Results - "genetics"

Haptoglobin phenotype and intensive glycemic control for coronary artery disease risk reduction in people with type two diabetes: The Veterans Affairs Diabetes Trial by Leah E Cahill, Rachel A Warren, Gideon D Bahn, Allie S Carew, Andrew P Levy, John Sapp, Eric B Rimm, Peter Reaven

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The effect of oxythioquinox exposure on normal human mammary epithelial cell gene expression: A microarray analysis study by Weston Ainsley, Whipkey Diana L, Gwinn Maureen R

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Experimental Therapeutic Solutions for Behcet’s Disease by Bozca BC, Alpsoy E

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What makes community engagement effective?: Lessons from the Eliminate Dengue Program in Queensland Australia. by Pamela A Kolopack, Janet A Parsons, James V Lavery

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Somatic development in children with Shwachman-Diamond syndrome by Agnieszka Bogusz-Wójcik, Honorata Kołodziejczyk, Maja Klaudel-Dreszler, Grzegorz Oracz, Joanna Pawłowska, Mieczysław Szalecki

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Epidemiology and In Vitro Activity of Ceftazidime/Avibactam, Meropenem/Vaborbactam and Imipenem/Relebactam against <i>KPC</i>-Producing <i>K. pneumoniae</i> Collected from Bacterem... by Federica Bovo, Donatella Lombardo, Tiziana Lazzarotto, Simone Ambretti, Paolo Gaibani

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Clinical features and enzyme replacement therapy in 10 children with Fabry disease by Qian Li, Qian Li, Jing Wang, Jing Wang, Minle Tian, Zhenle Yang, Zhenle Yang, Lichun Yu, Lichun Yu, Suwen Liu, Suwen Liu, Cong Wang, Cong Wang, Xiaoyuan Wang, Xiaoyuan Wang, Shuzhen Sun, Shuzhen Sun

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Naringenin modulates oxidative stress and lipid metabolism: Insights from network pharmacology, mendelian randomization, and molecular docking by Jian Gao, Linjie Yuan, Huanyu Jiang, Ganggang Li, Yuwei Zhang, Ruijun Zhou, Wenjia Xian, Yutong Zou, Quanyu Du, Quanyu Du, Xianhua Zhou

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Relação entre a patogenicidade do Schistosoma mansoni em camundongos e a susceptibilidade do molusco vetor: III. Mortalidade, pesos corporal e das vísceras Relationship between... by Eliana Maria Zanotti-Magalhães, Luiz Augusto Magalhães, José Ferreira de Carvalho

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Catheter-related candidemia and identification of causative Candida species in patients with cardiovascular disorder by Shirinsadat Hashemi Fesharaki, Seyed Reza Aghili, Tahereh Shokohi, Mohammad Ali Boroumand

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Education differences in sickness absence and the role of health behaviors: a prospective twin study by K. B. Seglem, R. Ørstavik, F. A. Torvik, E. Røysamb, M. Vollrath

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In vivo expression of Salmonella enterica serotype Typhi genes in the blood of patients with typhoid fever in Bangladesh. by Alaullah Sheikh, Richelle C Charles, Nusrat Sharmeen, Sean M Rollins, Jason B Harris, Md Saruar Bhuiyan, Mohammad Arifuzzaman, Farhana Khanam, Archana Bukka, Anuj Kalsy, Steffen Porwollik, Daniel T Leung, W Abdullah Brooks, Regina C LaRocque, Elizabeth L Hohmann, Alejandro Cravioto, Tanya Logvinenko, Stephen B Calderwood, Michael McClelland, James E Graham, Firdausi Qadri, Edward T Ryan

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Heterozygous familial hypercholesterolaemia in a pair of identical twins: a case report and updated review by Noor Shafina Mohd Nor, Alyaa Mahmood Al-Khateeb, Yung-An Chua, Noor Alicezah Mohd Kasim, Hapizah Mohd Nawawi

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Neonatal hemochromatosis with εγδβ-thalassemia: a case report and analysis of serum iron regulators by Mitsuru Tsuge, Aya Kodera, Hiromi Sumitomo, Tooru Araki, Ryuichi Yoshida, Kazuya Yasui, Hiroki Sato, Yosuke Washio, Kana Washio, Kenji Shigehara, Masato Yashiro, Takahito Yagi, Hirokazu Tsukahara

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Association of NQO2 With UDP-Glucuronosyltransferases Reduces Menadione Toxicity in Neuroblastoma Cells by Monivan Chhour, Pierre Perio, Regis Gayon, Hélène Ternet-Fontebasso, Gilles Ferry, Françoise Nepveu, Jean A. Boutin, Jean A. Boutin, Jan Sudor, Karine Reybier

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Fate of adipocyte progenitors during adipogenesis in mice fed a high-fat diet by Muhammad Bilal, Allah Nawaz, Tomonobu Kado, Muhammad Rahil Aslam, Yoshiko Igarashi, Ayumi Nishimura, Yoshiyuki Watanabe, Takahide Kuwano, Jianhui Liu, Hiroyuki Miwa, Takumi Era, Koichi Ikuta, Johji Imura, Kunimasa Yagi, Takashi Nakagawa, Shiho Fujisaka, Kazuyuki Tobe

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A case of dystonia with polycythemia and hypermanganesemia caused by SLC30A10 mutation: a treatable inborn error of manganese metabolism by Azita Tavasoli, Khadije Arjmandi Rafsanjani, Saba Hemmati, Marziyeh Mojbafan, Elham Zarei, Soudabeh Hosseini

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DNA methylation differences in monozygotic twins with Van der Woude syndrome by A. L. Petrin, E. Zeng, M. A. Thomas, D. Moretti-Ferreira, M. L. Marazita, X. J. Xie, J. C. Murray, L. M. Moreno-Uribe

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Peroxisomal Proliferator-Activated Receptor β/δ Deficiency Induces Cognitive Alterations by Triana Espinosa-Jiménez, Triana Espinosa-Jiménez, Triana Espinosa-Jiménez, Oriol Busquets, Amanda Cano, Amanda Cano, Amanda Cano, Amanda Cano, Elena Sánchez-López, Elena Sánchez-López, Elena Sánchez-López, Elena Sánchez-López, Ester Verdaguer, Ester Verdaguer, Ester Verdaguer, Antoni Parcerisas, Jordi Olloquequi, Carme Auladell, Carme Auladell, Carme Auladell, Jaume Folch, Jaume Folch, Walter Wahli, Walter Wahli, Walter Wahli, Manuel Vázquez-Carrera, Manuel Vázquez-Carrera, Manuel Vázquez-Carrera, Antoni Camins, Antoni Camins, Antoni Camins, Miren Ettcheto, Miren Ettcheto, Miren Ettcheto

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Recurrent c.G1636A (p.G546S) mutation of COL2A1 in a Chinese family with skeletal dysplasia and different metaphyseal changes: a case report by Jing Chen, Xiaomin Ma, Yulin Zhou, Guimei Li, Qiwei Guo

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