Armadillo Domain Proteins

"Armadillo Domain 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

A family of proteins that contain several 42-amino acid repeat domains and are homologous to the Drosophila armadillo protein. They bind to other proteins through their armadillo domains and play a variety of roles in the CELL including SIGNAL TRANSDUCTION, regulation of DESMOSOME assembly, and CELL ADHESION.

Descriptor ID	D051186
MeSH Number(s)	D12.776.091
Concept/Terms	Armadillo Domain Proteins Armadillo Domain Proteins Armadillo Proteins Arm Motif Proteins Armadillo Motif Proteins Armadillo Repeat Containing Proteins Armadillo Protein Family

Below are MeSH descriptors whose meaning is more general than "Armadillo Domain Proteins".

Chemicals and Drugs [D]
Amino Acids, Peptides, and Proteins [D12]
Proteins [D12.776]
Armadillo Domain Proteins [D12.776.091]

Below are MeSH descriptors whose meaning is related to "Armadillo Domain Proteins".

Below are MeSH descriptors whose meaning is more specific than "Armadillo Domain Proteins".

Armadillo Domain Proteins
beta Catenin
gamma Catenin
Plakophilins

publications

Timeline | Most Recent

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

Bar chart showing 18 publications over 14 distinct years, with a maximum of 2 publications in 2009 and 2018 and 2019 and 2020

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

Year	Major Topic	Minor Topic	Total
1997	0	1	1
2003	0	1	1
2009	1	1	2
2012	1	0	1
2013	1	0	1
2015	0	1	1
2016	1	0	1
2018	1	1	2
2019	2	0	2
2020	2	0	2
2021	1	0	1
2022	1	0	1
2023	0	1	1
2025	1	0	1

Below are the most recent publications written about "Armadillo Domain Proteins" by people in Profiles.

Dogan EO, Simonini SR, Bouley J, Weiss A, Brown RH, Henninger N. Genetic Ablation of Sarm1 Mitigates Disease Acceleration after Traumatic Brain Injury in the SOD1G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis. Ann Neurol. 2025 May; 97(5):963-975.

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Icso JD, Thompson PR. A phase transition reduces the threshold for nicotinamide mononucleotide-based activation of SARM1, an NAD(P) hydrolase, to physiologically relevant levels. J Biol Chem. 2023 11; 299(11):105284.

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Icso JD, Thompson PR. The chemical biology of NAD+ regulation in axon degeneration. Curr Opin Chem Biol. 2022 08; 69:102176.

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Sambashivan S, Freeman MR. SARM1 signaling mechanisms in the injured nervous system. Curr Opin Neurobiol. 2021 08; 69:247-255.

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Peters OM, Weiss A, Metterville J, Song L, Logan R, Smith GA, Schwarzschild MA, Mueller C, Brown RH, Freeman M. Genetic diversity of axon degenerative mechanisms in models of Parkinson's disease. Neurobiol Dis. 2021 07; 155:105368.

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Hsu JM, Kang Y, Corty MM, Mathieson D, Peters OM, Freeman MR. Injury-Induced Inhibition of Bystander Neurons Requires dSarm and Signaling from Glia. Neuron. 2021 02 03; 109(3):473-487.e5.

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Loring HS, Parelkar SS, Mondal S, Thompson PR. Identification of the first noncompetitive SARM1 inhibitors. Bioorg Med Chem. 2020 09 15; 28(18):115644.

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Loring HS, Icso JD, Nemmara VV, Thompson PR. Initial Kinetic Characterization of Sterile Alpha and Toll/Interleukin Receptor Motif-Containing Protein 1. Biochemistry. 2020 03 03; 59(8):933-942.

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Loring HS, Thompson PR. Emergence of SARM1 as a Potential Therapeutic Target for Wallerian-type Diseases. Cell Chem Biol. 2020 01 16; 27(1):1-13.

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Carty M, Kearney J, Shanahan KA, Hams E, Sugisawa R, Connolly D, Doran CG, Mu?oz-Wolf N, G?rtler C, Fitzgerald KA, Lavelle EC, Fallon PG, Bowie AG. Cell Survival and Cytokine Release after Inflammasome Activation Is Regulated by the Toll-IL-1R Protein SARM. Immunity. 2019 06 18; 50(6):1412-1424.e6.

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