Major Histocompatibility Complex
"Major Histocompatibility Complex" 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.
The genetic region which contains the loci of genes which determine the structure of the serologically defined (SD) and lymphocyte-defined (LD) TRANSPLANTATION ANTIGENS, genes which control the structure of the IMMUNE RESPONSE-ASSOCIATED ANTIGENS, HUMAN; the IMMUNE RESPONSE GENES which control the ability of an animal to respond immunologically to antigenic stimuli, and genes which determine the structure and/or level of the first four components of complement.
Descriptor ID |
D008285
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MeSH Number(s) |
G05.360.340.024.340.610 G05.360.340.024.380.500 G12.500.500
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Concept/Terms |
Major Histocompatibility Complex- Major Histocompatibility Complex
- Complex, Major Histocompatibility
- Complices, Major Histocompatibility
- Histocompatibility Complex, Major
- Histocompatibility Complices, Major
- Major Histocompatibility Complices
- Histocompatibility Complex
- Complex, Histocompatibility
- Complices, Histocompatibility
- Histocompatibility Complices
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Below are MeSH descriptors whose meaning is more general than "Major Histocompatibility Complex".
Below are MeSH descriptors whose meaning is more specific than "Major Histocompatibility Complex".
This graph shows the total number of publications written about "Major Histocompatibility Complex" by people in this website by year, and whether "Major Histocompatibility Complex" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 2 | 4 | 6 | 1996 | 1 | 0 | 1 | 1997 | 0 | 1 | 1 | 1998 | 0 | 1 | 1 | 1999 | 0 | 1 | 1 | 2000 | 0 | 1 | 1 | 2001 | 3 | 1 | 4 | 2002 | 2 | 1 | 3 | 2003 | 3 | 0 | 3 | 2004 | 2 | 3 | 5 | 2005 | 2 | 1 | 3 | 2006 | 6 | 0 | 6 | 2007 | 1 | 1 | 2 | 2008 | 1 | 2 | 3 | 2009 | 2 | 2 | 4 | 2010 | 1 | 2 | 3 | 2011 | 1 | 1 | 2 | 2012 | 1 | 2 | 3 | 2013 | 1 | 1 | 2 | 2015 | 0 | 1 | 1 | 2016 | 2 | 1 | 3 | 2017 | 1 | 2 | 3 | 2018 | 1 | 0 | 1 | 2020 | 0 | 1 | 1 | 2021 | 0 | 2 | 2 | 2023 | 1 | 0 | 1 | 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Major Histocompatibility Complex" by people in Profiles.
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Wade KJ, Suseno R, Kizer K, Williams J, Boquett J, Caillier S, Pollock NR, Renschen A, Santaniello A, Oksenberg JR, Norman PJ, Augusto DG, Hollenbach JA. MHConstructor: a high-throughput, haplotype-informed solution to the MHC assembly challenge. Genome Biol. 2024 Oct 17; 25(1):274.
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Pollock NR, Farias TDJ, Kichula KM, Sauter J, Scholz S, Nii-Trebi NI, Khor SS, Tokunaga K, Voorter CE, Groeneweg M, Augusto DG, Arrieta-Bola?os E, Mayor NP, Edinur HA, ElGhazali G, Issler HC, Petzl-Erler ML, Oksenberg JR, Marin WM, Hollenbach JA, Gendzekhadze K, Cita R, Stelet V, Rajalingam R, Koskela S, Clancy J, Chatzistamatiou T, Houwaart T, Kulski J, Guethlein LA, Parham P, Schmidt AH, Dilthey A, Norman PJ. The 18th International HLA & Immunogenetics workshop project report: Creating fully representative MHC reference haplotypes. HLA. 2024 06; 103(6):e15568.
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Houwaart T, Scholz S, Pollock NR, Palmer WH, Kichula KM, Strelow D, Le DB, Belick D, H?lse L, Lautwein T, Wachtmeister T, Wollenweber TE, Henrich B, K?hrer K, Parham P, Guethlein LA, Norman PJ, Dilthey AT. Complete sequences of six major histocompatibility complex haplotypes, including all the major MHC class II structures. HLA. 2023 07; 102(1):28-43.
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Johnson AM, Boland JM, Wrobel J, Klezcko EK, Weiser-Evans M, Hopp K, Heasley L, Clambey ET, Jordan K, Nemenoff RA, Schenk EL. Cancer Cell-Specific Major Histocompatibility Complex II Expression as a Determinant of the Immune Infiltrate Organization and Function in the NSCLC Tumor Microenvironment. J Thorac Oncol. 2021 10; 16(10):1694-1704.
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Bai P, Zhou Q, Wei P, Bai H, Chan SK, Kappler JW, Marrack P, Yin L. Rational discovery of a cancer neoepitope harboring the KRAS G12D driver mutation. Sci China Life Sci. 2021 12; 64(12):2144-2152.
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Menasche BL, Davis EM, Wang S, Ouyang Y, Li S, Yu H, Shen J. PBRM1 and the glycosylphosphatidylinositol biosynthetic pathway promote tumor killing mediated by MHC-unrestricted cytotoxic lymphocytes. Sci Adv. 2020 11; 6(48).
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Askar M, Sayer D, Wang T, Haagenson M, Spellman SR, Lee SJ, Madbouly A, Fleischhauer K, Hsu KC, Verneris MR, Thomas D, Zhang A, Sobecks RM, Majhail NS. Analysis of Single Nucleotide Polymorphisms in the Gamma Block of the Major Histocompatibility Complex in Association with Clinical Outcomes of Hematopoietic Cell Transplantation: A Center for International Blood and Marrow Transplant Research Study. Biol Blood Marrow Transplant. 2019 04; 25(4):664-672.
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Marrack P, Krovi SH, Silberman D, White J, Kushnir E, Nakayama M, Crooks J, Danhorn T, Leach S, Anselment R, Scott-Browne J, Gapin L, Kappler J. The somatically generated portion of T cell receptor CDR3a contributes to the MHC allele specificity of the T cell receptor. Elife. 2017 11 17; 6.
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Redondo MJ, Steck AK, Pugliese A. Genetics of type 1 diabetes. Pediatr Diabetes. 2018 05; 19(3):346-353.
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Wang Y, Singh NK, Spear TT, Hellman LM, Piepenbrink KH, McMahan RH, Rosen HR, Vander Kooi CW, Nishimura MI, Baker BM. How an alloreactive T-cell receptor achieves peptide and MHC specificity. Proc Natl Acad Sci U S A. 2017 06 13; 114(24):E4792-E4801.
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