Intercellular Signaling Peptides and Proteins

"Intercellular Signaling Peptides and Proteins" 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

Regulatory proteins and peptides that are signaling molecules involved in the process of PARACRINE COMMUNICATION. They are generally considered factors that are expressed by one cell and are responded to by receptors on another nearby cell. They are distinguished from HORMONES in that their actions are local rather than distal.

Descriptor ID	D036341
MeSH Number(s)	D12.644.276 D12.776.467 D23.529
Concept/Terms	Intercellular Signaling Peptides and Proteins Intercellular Signaling Peptides and Proteins Paracrine Peptide Factors Paracrine Peptide Factors Peptide Factors, Paracrine Paracrine Protein Factors Paracrine Protein Factors Growth Factors Growth Factors

Below are MeSH descriptors whose meaning is more general than "Intercellular Signaling Peptides and Proteins".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Peptides [D12.644]
Intercellular Signaling Peptides and Proteins [D12.644.276]
Proteins [D12.776]
Intercellular Signaling Peptides and Proteins [D12.776.467]
Biological Factors [D23]
Intercellular Signaling Peptides and Proteins [D23.529]

Below are MeSH descriptors whose meaning is related to "Intercellular Signaling Peptides and Proteins".

Below are MeSH descriptors whose meaning is more specific than "Intercellular Signaling Peptides and Proteins".

publications

Timeline | Most Recent

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

Bar chart showing 87 publications over 21 distinct years, with a maximum of 15 publications in 2008

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

Year	Major Topic	Minor Topic	Total
1995	1	0	1
1999	1	0	1
2001	0	1	1
2002	3	1	4
2003	5	4	9
2004	4	3	7
2005	3	1	4
2006	3	1	4
2007	6	4	10
2008	8	7	15
2009	4	2	6
2010	0	4	4
2011	0	4	4
2012	2	3	5
2013	1	1	2
2014	3	1	4
2016	1	0	1
2017	0	1	1
2018	0	2	2
2019	0	1	1
2022	0	1	1

Below are the most recent publications written about "Intercellular Signaling Peptides and Proteins" by people in Profiles.

Tanaka Y, Kusumoto SY, Honma Y, Takeya K, Eto M. Overexpression of progranulin increases pathological protein accumulation by suppressing autophagic flux. Biochem Biophys Res Commun. 2022 06 30; 611:78-84.

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Wimmer RA, Leopoldi A, Aichinger M, Wick N, Hantusch B, Novatchkova M, Taubenschmid J, H?mmerle M, Esk C, Bagley JA, Lindenhofer D, Chen G, Boehm M, Agu CA, Yang F, Fu B, Zuber J, Knoblich JA, Kerjaschki D, Penninger JM. Human blood vessel organoids as a?model of?diabetic vasculopathy. Nature. 2019 01; 565(7740):505-510.

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Zhao G, Huang BL, Rigueur D, Wang W, Bhoot C, Charles KR, Baek J, Mohan S, Jiang J, Lyons KM. CYR61/CCN1 Regulates Sclerostin Levels and Bone Maintenance. J Bone Miner Res. 2018 06; 33(6):1076-1089.

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Branchford BR, Stalker TJ, Law L, Acevedo G, Sather S, Brzezinski C, Wilson KM, Minson K, Lee-Sherick AB, Davizon-Castillo P, Ng C, Zhang W, Neeves KB, Lentz SR, Wang X, Frye SV, Shelton Earp H, DeRyckere D, Brass LF, Graham DK, Di Paola JA. The small-molecule MERTK inhibitor UNC2025 decreases platelet activation and prevents thrombosis. J Thromb Haemost. 2018 02; 16(2):352-363.

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Wiest DL. THEMIS-tery is solved. Nat Immunol. 2017 03 22; 18(4):368-370.

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Neill T, Buraschi S, Goyal A, Sharpe C, Natkanski E, Schaefer L, Morrione A, Iozzo RV. EphA2 is a functional receptor for the growth factor progranulin. J Cell Biol. 2016 Dec 05; 215(5):687-703.

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Briot A, Jaroszewicz A, Warren CM, Lu J, Touma M, Rudat C, Hofmann JJ, Airik R, Weinmaster G, Lyons K, Wang Y, Kispert A, Pellegrini M, Iruela-Arispe ML. Repression of Sox9 by Jag1 is continuously required to suppress the default chondrogenic fate of vascular smooth muscle cells. Dev Cell. 2014 Dec 22; 31(6):707-21.

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Shekels LL, Colvin Wanshura LE, Xie Y, Nelson MS, Stephenson EJ, Khan SA, Gupta P. The effects of Gremlin1 on human umbilical cord blood hematopoietic progenitors. Blood Cells Mol Dis. 2015 Jan; 54(1):103-9.

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Klinkhammer BM, Kramann R, Mallau M, Makowska A, van Roeyen CR, Rong S, Buecher EB, Boor P, Kovacova K, Zok S, Denecke B, Stuettgen E, Otten S, Floege J, Kunter U. Mesenchymal stem cells from rats with chronic kidney disease exhibit premature senescence and loss of regenerative potential. PLoS One. 2014; 9(3):e92115.

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Gibson DA, Tymanskyj S, Yuan RC, Leung HC, Lefebvre JL, Sanes JR, Chédotal A, Ma L. Dendrite self-avoidance requires cell-autonomous slit/robo signaling in cerebellar purkinje cells. Neuron. 2014 Mar 05; 81(5):1040-1056.

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