Zobrazeno 1 - 10
of 2 163
pro vyhledávání: '"PPARG, Peroxisome Proliferator Activated Receptor Gamma"'
Autor:
Sreeparna Banerjee, Erhan Astarci
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on PPARG (peroxisome proliferator-activated receptor gamma), with data on DNA, on the protein encoded, and where the gene is implicated.
Autor:
Uzar, Izabela, Bogacz, Anna, Łuszczyńska, Małgorzata, Wolek, Marlena, Kotrych, Katarzyna, Modrzejewski, Andrzej, Czerny, Bogusław, Ziętek, Paweł, Kamiński, Adam
Publikováno v:
Biomedicines; Jul2024, Vol. 13 Issue 7, p1440, 13p
Autor:
Khokhar, Manoj1 (AUTHOR), Purohit, Purvi1 (AUTHOR) dr.purvipurohit@gmail.com, Gadwal, Ashita1 (AUTHOR), Tomo, Sojit1 (AUTHOR), Bajpai, Nitin Kumar2 (AUTHOR), Shukla, Ravindra3 (AUTHOR)
Publikováno v:
JMIR Bioinformatics & Biotechnology. 2023, Vol. 4 Issue 1, p1-24. 24p.
Publikováno v:
Pharmacology & Therapeutics
COVID-19 has remained an uncontained, worldwide pandemic. While battling for the disease in China, six Traditional Chinese Medicine (TCM) recipes have been shown to be remarkably effective for treating patients with COVID-19. The present review discu
Autor:
Steven J. Fliesler, Sriganesh Ramachandra Rao, Sithara Raju Ponny, Ned A. Porter, Shailendra B. Patel, Vincent Fong, Babu Nageswararao Kanuri, Keri A. Tallman
Publikováno v:
Journal of Lipid Research, Vol 62, Iss, Pp 100002-(2021)
Journal of Lipid Research
Journal of Lipid Research
Smith-Lemli-Opitz Syndrome (SLOS) is a developmental disorder (OMIM #270400) caused by autosomal recessive mutations in the Dhcr7 gene, which encodes the enzyme 3β-hydroxysterol-Δ7 reductase. SLOS patients present clinically with dysmorphology and
Akademický článek
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Autor:
Martin Bidlingmaier, Birgit Rathkolb, Martin Hrabĕ de Angelis, Arne Hinrichs, Werner F. Blum, Sebastian Bultmann, Heinrich Leonhardt, Maik Dahlhoff, Simone Renner, Andreas Blutke, Eckhard Wolf, Barbara Kessler, Andreas Hoeflich, Hiroshi Nagashima, Maren Bernau, Mayuko Kurome, Rüdiger Wanke, Elisabeth Kemter, Armin M. Scholz
Publikováno v:
Molecular Metabolism, Vol 11, Iss, Pp 113-128 (2018)
Molecular Metabolism
Mol. Metab. 11, 113-128 (2018)
Molecular metabolism, 11: 113-128
Molecular Metabolism
Mol. Metab. 11, 113-128 (2018)
Molecular metabolism, 11: 113-128
Objective Laron syndrome (LS) is a rare, autosomal recessive disorder in humans caused by loss-of-function mutations of the growth hormone receptor (GHR) gene. To establish a large animal model for LS, pigs with GHR knockout (KO) mutations were gener
Publikováno v:
Translational Oncology, Vol 14, Iss 7, Pp 101089-(2021)
Translational Oncology
Translational Oncology
Highlights • Diabetes mellitus and hyperglycemia significantly affect the incidence and prognosis of colorectal cancer. • Evidence of the effects of metformin remain controversial in cancer prognosis. • Potential molecular mechanisms by which D
Autor:
Vetrivel, Sharmilee, Tamburello, Mariangela, Oßwald, Andrea, Ru Zhang, Khan, Ali, Sara Jung, Baker, Jessica E., Rainey, William E., Nowak, Elisabeth, Altieri, Barbara, Detomas, Mario, Watts, Deepika, Williams, Tracy Ann, Wielockx, Ben, Beuschlein, Felix, Reincke, Martin, Sbiera, Silviu, Riester, Anna
Publikováno v:
Frontiers in Endocrinology; 2023, p1-14, 14p
Autor:
Mishra, Shailja1 (AUTHOR), Maurya, Vimal K2 (AUTHOR), Kumar, Swatantra2 (AUTHOR), Ankita1 (AUTHOR), Kaur, Apjit1 (AUTHOR) apjitkaur@kgmcindia.edu, Saxena, Shailendra K2 (AUTHOR) shailen@kgmcindia.edu
Publikováno v:
Current Eye Research. Nov2020, Vol. 45 Issue 11, p1325-1341. 17p.