Academic literature on the topic 'SMIM10'

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Journal articles on the topic "SMIM10"

1

Kulinska, Karolina Iwona, Mirosław Andrusiewicz, Anna Dera-Szymanowska, et al. "Phoenixin as a New Target in the Development of Strategies for Endometriosis Diagnosis and Treatment." Biomedicines 9, no. 10 (2021): 1427. http://dx.doi.org/10.3390/biomedicines9101427.

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Small integral membrane protein 20/phoenixin (SMIM20/PNX) and its receptor GPR173 (G Protein-Coupled Receptor 173) play a role in the regulation of the hypothalamic–pituitary–gonadal axis (HPG). The aim of the study was to determine PNX, FSH, LH, and 17β-estradiol association in women with endometriosis, and the expression of SMIM20/PNX signaling via GPR173. Serum PNX, FSH, LH, and 17β-estradiol concentrations were measured by enzyme and electrochemiluminescence immunoassay. SMIM20/PNX and GPR173 expression in the eutopic and ectopic endometrium was assessed by qPCR and immunohistochemistry. R
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2

Nett, Jeniel E., Hiram Sanchez, Michael T. Cain, Kelly M. Ross, and David R. Andes. "Interface of Candida albicans Biofilm Matrix-Associated Drug Resistance and Cell Wall Integrity Regulation." Eukaryotic Cell 10, no. 12 (2011): 1660–69. http://dx.doi.org/10.1128/ec.05126-11.

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ABSTRACTCandida albicansfrequently infects medical devices by growing as a biofilm, i.e., a community of adherent organisms entrenched in an extracellular matrix. During biofilm growth,Candidaspp. acquire the ability to resist high concentrations of antifungal drugs. One recently recognized biofilm resistance mechanism involves drug sequestration by matrix β-1,3 glucan. Using a candidate gene approach, we investigated potentialC. albicansβ-1,3-glucan regulators, based on their homology toSaccharomyces cerevisiae, includingSMI1and protein kinase C (PKC) pathway components. We identified a role
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3

Brilhante, Raimunda Sâmia Nogueira, Xhaulla Maria Quariguasi Cunha Fonseca, Vandbergue Santos Pereira, et al. "In vitro inhibitory effect of statins on planktonic cells and biofilms of the Sporothrix schenckii species complex." Journal of Medical Microbiology 69, no. 6 (2020): 838–43. http://dx.doi.org/10.1099/jmm.0.001195.

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Introduction. Sporotrichosis, caused by species of the Sporothrix schenckii complex, is the most prevalent subcutaneous mycosis in many areas of Latin America. Statins are a class of drugs widely used for lowering high sterol levels through their action on 3-hydroxy-3-methylglutaryl-CoA reductase, a key enzyme in the synthesis of sterol. Aim. In this study, the antifungal activity of statins (simvastatin, atorvastatin, pravastatin) against planktonic cells and biofilms of S. schenckii complex species was evaluated, as well as the interaction of pravastatin with classical antifungals (amphoteri
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4

Yu, Ying, Zhejiong Wang, Linchao Zhu, Yushiang Lin, Haochun Chang, and Huaxi Xu. "The Polymorphism of SMIM1 Gene in Chinese Dividuals." Indian Journal of Hematology and Blood Transfusion 35, no. 1 (2018): 137–43. http://dx.doi.org/10.1007/s12288-018-0963-8.

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5

Ballif, Bryan A., Virginie Helias, Thierry Peyrard, et al. "Disruption of SMIM1 causes the Vel− blood type." EMBO Molecular Medicine 5, no. 5 (2013): 751–61. http://dx.doi.org/10.1002/emmm.201302466.

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6

Rajeswari, Jithine Jayakumar, Ayelén Melisa Blanco, and Suraj Unniappan. "Phoenixin-20 suppresses food intake, modulates glucoregulatory enzymes, and enhances glycolysis in zebrafish." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 318, no. 5 (2020): R917—R928. http://dx.doi.org/10.1152/ajpregu.00019.2020.

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Phoenixin is a 20-amino acid peptide (PNX-20) cleaved from the small integral membrane protein 20 (SMIM20), with multiple biological roles in mammals. However, its role in nonmammalian vertebrates is poorly understood. This research aimed to determine whether PNX-20 influences feeding and metabolism in zebrafish. The mRNAs encoding SMIM20 and its putative receptor, super conserved receptor expressed in brain 3 (SREB3), are present in both central and peripheral tissues of zebrafish. Immunohistochemical analysis confirmed the presence of PNX-like immunoreactivity in the gut and in zebrafish liv
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7

Davis, D. R., J. P. Brion, A. M. Couck та ін. "The phosphorylation state of the microtubule-associated protein tau as affected by glutamate, colchicine and β-amyloid in primary rat cortical neuronal cultures". Biochemical Journal 309, № 3 (1995): 941–49. http://dx.doi.org/10.1042/bj3090941.

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The effects of the excitatory amino acid glutamate, the microtubule destabilizing agent colchicine, and beta 25-35-amyloid peptide on the phosphorylation state of tau were studied in rat cortical neurons in primary culture. Using immunocytochemistry and Western-blot analysis, we demonstrated that a proportion of tau in these cultures is normally highly phosphorylated, but most of this tau fraction is dephosphorylated after treatment of the cultures with glutamate or colchicine, but not with beta-amyloid; the glutamate- and colchicine-induced changes in tau phosphorylation commenced before cell
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8

Unfried, Juan Pablo, and Puri Fortes. "SMIM30, a tiny protein with a big role in liver cancer." Journal of Hepatology 73, no. 5 (2020): 1010–12. http://dx.doi.org/10.1016/j.jhep.2020.07.015.

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9

Barrese, Vincenzo, Jennifer B. Stott, Samuel N. Baldwin, Gema Mondejar-Parreño, and Iain A. Greenwood. "SMIT (Sodium-Myo-Inositol Transporter) 1 Regulates Arterial Contractility Through the Modulation of Vascular Kv7 Channels." Arteriosclerosis, Thrombosis, and Vascular Biology 40, no. 10 (2020): 2468–80. http://dx.doi.org/10.1161/atvbaha.120.315096.

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Objective: The SMIT1 (sodium:myo-inositol transporter 1) regulates myo-inositol movement into cells and responses to hypertonic stimuli. Alteration of myo-inositol levels has been associated with several diseases, including hypertension, but there is no evidence of a functional role of SMIT1 in the vasculature. Recent evidence showed that in the nervous system SMIT1 interacted and modulated the function of members of the Kv7 family of voltage-gated potassium channels, which are also expressed in the vasculature where they regulate arterial contractility. Therefore, in this study, we evaluated
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10

Aniweh, Yaw, Prince B. Nyarko, Evelyn Quansah, Laty Gaye Thiam, and Gordon A. Awandare. "SMIM1 at a glance; discovery, genetic basis, recent progress and perspectives." Parasite Epidemiology and Control 5 (May 2019): e00101. http://dx.doi.org/10.1016/j.parepi.2019.e00101.

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