Receptors, Adrenergic, beta

"Receptors, Adrenergic, beta" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

One of two major pharmacologically defined classes of adrenergic receptors. The beta adrenergic receptors play an important role in regulating CARDIAC MUSCLE contraction, SMOOTH MUSCLE relaxation, and GLYCOGENOLYSIS.

Descriptor ID	D011943
MeSH Number(s)	D12.776.543.750.670.300.300.340 D12.776.543.750.695.150.300.340 D12.776.543.750.720.330.300.340
Concept/Terms	Receptors, Adrenergic, beta Receptors, Adrenergic, beta Adrenergic beta-Receptors Adrenergic beta Receptors beta-Receptors, Adrenergic Receptors, beta-Adrenergic Receptors, beta Adrenergic Receptor, Adrenergic, beta beta-Adrenergic Receptors beta Adrenergic Receptors

Below are MeSH descriptors whose meaning is more general than "Receptors, Adrenergic, beta".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Membrane Proteins [D12.776.543]
Receptors, Cell Surface [D12.776.543.750]
Receptors, Biogenic Amine [D12.776.543.750.670]
Receptors, Catecholamine [D12.776.543.750.670.300]
Receptors, Adrenergic [D12.776.543.750.670.300.300]
Receptors, Adrenergic, beta [D12.776.543.750.670.300.300.340]
Receptors, G-Protein-Coupled [D12.776.543.750.695]
Receptors, Catecholamine [D12.776.543.750.695.150]
Receptors, Adrenergic [D12.776.543.750.695.150.300]
Receptors, Adrenergic, beta [D12.776.543.750.695.150.300.340]
Receptors, Neurotransmitter [D12.776.543.750.720]
Receptors, Catecholamine [D12.776.543.750.720.330]
Receptors, Adrenergic [D12.776.543.750.720.330.300]
Receptors, Adrenergic, beta [D12.776.543.750.720.330.300.340]

Below are MeSH descriptors whose meaning is related to "Receptors, Adrenergic, beta".

Below are MeSH descriptors whose meaning is more specific than "Receptors, Adrenergic, beta".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Receptors, Adrenergic, beta" by people in this website by year, and whether "Receptors, Adrenergic, beta" was a major or minor topic of these publications.

Bar chart showing 18 publications over 12 distinct years, with a maximum of 2 publications in 1994 and 1998 and 2009 and 2013 and 2017 and 2018

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1994	1	1	2
1998	0	2	2
1999	0	1	1
2002	0	1	1
2003	0	1	1
2008	1	0	1
2009	1	1	2
2013	1	1	2
2014	0	1	1
2017	1	1	2
2018	1	1	2
2019	0	1	1

Below are the most recent publications written about "Receptors, Adrenergic, beta" by people in Profiles.

LaRocca TJ, Altman P, Jarrah AA, Gordon R, Wang E, Hadri L, Burke MW, Haddad GE, Hajjar RJ, Tarzami ST. CXCR4 Cardiac Specific Knockout Mice Develop a Progressive Cardiomyopathy. Int J Mol Sci. 2019 May 08; 20(9).

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Sierra-Fonseca JA, Bracamontes C, Saldecke J, Das S, Roychowdhury S. Activation of ?- and a2-adrenergic receptors stimulate tubulin polymerization and promote the association of G?? with microtubules in cultured NIH3T3 cells. Biochem Biophys Res Commun. 2018 09 03; 503(1):102-108.

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Nguyen MN, Su Y, Vizi D, Fang L, Ellims AH, Zhao WB, Kiriazis H, Gao XM, Sadoshima J, Taylor AJ, McMullen JR, Dart AM, Kaye DM, Du XJ. Mechanisms responsible for increased circulating levels of galectin-3 in cardiomyopathy and heart failure. Sci Rep. 2018 05 29; 8(1):8213.

View in: PubMed
Ivey MJ, Kuwabara JT, Pai JT, Moore RE, Sun Z, Tallquist MD. Resident fibroblast expansion during cardiac growth and remodeling. J Mol Cell Cardiol. 2018 01; 114:161-174.

View in: PubMed
Ceholski DK, Turnbull IC, Pothula V, Lecce L, Jarrah AA, Kho C, Lee A, Hadri L, Costa KD, Hajjar RJ, Tarzami ST. CXCR4 and CXCR7 play distinct roles in cardiac lineage specification and pharmacologic ?-adrenergic response. Stem Cell Res. 2017 08; 23:77-86.

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Otis JM, Mueller D. Reversal of Cocaine-Associated Synaptic Plasticity in Medial Prefrontal Cortex Parallels Elimination of Memory Retrieval. Neuropsychopharmacology. 2017 Sep; 42(10):2000-2010.

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Yaniv Y, Ahmet I, Tsutsui K, Behar J, Moen JM, Okamoto Y, Guiriba TR, Liu J, Bychkov R, Lakatta EG. Deterioration of autonomic neuronal receptor signaling and mechanisms intrinsic to heart pacemaker cells contribute to age-associated alterations in heart rate variability in?vivo. Aging Cell. 2016 08; 15(4):716-24.

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Wang ER, Jarrah AA, Benard L, Chen J, Schwarzkopf M, Hadri L, Tarzami ST. Deletion of CXCR4 in cardiomyocytes exacerbates cardiac dysfunction following isoproterenol administration. Gene Ther. 2014 May; 21(5):496-506.

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Otis JM, Fitzgerald MK, Mueller D. Inhibition of hippocampal ?-adrenergic receptors impairs retrieval but not reconsolidation of cocaine-associated memory and prevents subsequent reinstatement. Neuropsychopharmacology. 2014 Jan; 39(2):303-10.

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Moreno-Smith M, Lee SJ, Lu C, Nagaraja AS, He G, Rupaimoole R, Han HD, Jennings NB, Roh JW, Nishimura M, Kang Y, Allen JK, Armaiz GN, Matsuo K, Shahzad MM, Bottsford-Miller J, Langley RR, Cole SW, Lutgendorf SK, Siddik ZH, Sood AK. Biologic effects of dopamine on tumor vasculature in ovarian carcinoma. Neoplasia. 2013 May; 15(5):502-10.

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