Polymorphism, Restriction Fragment Length

"Polymorphism, Restriction Fragment Length" 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

Variation occurring within a species in the presence or length of DNA fragment generated by a specific endonuclease at a specific site in the genome. Such variations are generated by mutations that create or abolish recognition sites for these enzymes or change the length of the fragment.

Descriptor ID	D012150
MeSH Number(s)	G05.365.795.595
Concept/Terms	Polymorphism, Restriction Fragment Length Polymorphism, Restriction Fragment Length RFLPs Restriction Fragment Length Polymorphisms Restriction Fragment Length Polymorphism RFLP

Below are MeSH descriptors whose meaning is more general than "Polymorphism, Restriction Fragment Length".

Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Polymorphism, Genetic [G05.365.795]
Polymorphism, Restriction Fragment Length [G05.365.795.595]

Below are MeSH descriptors whose meaning is related to "Polymorphism, Restriction Fragment Length".

Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Restriction Fragment Length".

publications

Timeline | Most Recent

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

Bar chart showing 40 publications over 17 distinct years, with a maximum of 7 publications in 1996

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

Year	Major Topic	Minor Topic	Total
1996	1	6	7
1997	0	2	2
1998	0	1	1
1999	0	3	3
2000	1	0	1
2001	0	2	2
2002	0	2	2
2003	2	0	2
2004	1	3	4
2005	0	3	3
2006	0	1	1
2007	0	2	2
2008	0	3	3
2010	0	2	2
2011	0	1	1
2012	1	2	3
2013	0	1	1

Below are the most recent publications written about "Polymorphism, Restriction Fragment Length" by people in Profiles.

Zeng-Brouwers J, Beckmann J, Nastase MV, Iozzo RV, Schaefer L. De novo expression of circulating biglycan evokes an innate inflammatory tissue response via MyD88/TRIF pathways. Matrix Biol. 2014 Apr; 35:132-42.

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Sarig O, Nahum S, Rapaport D, Ishida-Yamamoto A, Fuchs-Telem D, Qiaoli L, Cohen-Katsenelson K, Spiegel R, Nousbeck J, Israeli S, Borochowitz ZU, Padalon-Brauch G, Uitto J, Horowitz M, Shalev S, Sprecher E. Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation. Am J Hum Genet. 2012 Aug 10; 91(2):337-42.

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Scott AP, Laing NG, Mastaglia F, Dalakas M, Needham M, Allcock RJ. Investigation of NOTCH4 coding region polymorphisms in sporadic inclusion body myositis. J Neuroimmunol. 2012 Sep 15; 250(1-2):66-70.

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Borah BK, Dasgupta I. PCR-RFLP analysis indicates that recombination might be a common occurrence among the cassava infecting begomoviruses in India. Virus Genes. 2012 Oct; 45(2):327-32.

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Barnholtz-Sloan JS, Guan X, Zeigler-Johnson C, Meropol NJ, Rebbeck TR. Decision tree-based modeling of androgen pathway genes and prostate cancer risk. Cancer Epidemiol Biomarkers Prev. 2011 Jun; 20(6):1146-55.

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Hayes DF, Skaar TC, Rae JM, Henry NL, Nguyen AT, Stearns V, Li L, Philips S, Desta Z, Flockhart DA. Estrogen receptor genotypes, menopausal status, and the effects of tamoxifen on lipid levels: revised and updated results. Clin Pharmacol Ther. 2010 Nov; 88(5):626-9.

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Hasan R, Jabeen K, Ali A, Rafiq Y, Laiq R, Malik B, Tanveer M, Groenheit R, Ghebremichael S, Hoffner S, Hasan Z. Extensively drug-resistant tuberculosis, Pakistan. Emerg Infect Dis. 2010 Sep; 16(9):1473-5.

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Glas J, Beynon V, Bachstein B, Steckenbiller J, Manolis V, Euba A, M?ller-Myhsok B, Folwaczny M. Increased plasma concentration of surfactant protein D in chronic periodontitis independent of SFTPD genotype: potential role as a biomarker. Tissue Antigens. 2008 Jul; 72(1):21-8.

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Wahl C, Kautzmann S, Krebiehl G, Strauss K, Woitalla D, M?ller T, Bauer P, Riess O, Kr?ger R. A comprehensive genetic study of the proteasomal subunit S6 ATPase in German Parkinson's disease patients. J Neural Transm (Vienna). 2008 Aug; 115(8):1141-8.

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Piovesan EJ, Sobreira CF, Scola RH, Lorenzoni PJ, Lange MC, Werneck LC, Smith D, Silberstein S. Episodic migraine associated with postural orthostatic tachycardia syndrome and vasovagal syncope: migraine triggers neuromediated syncope. Arq Neuropsiquiatr. 2008 Mar; 66(1):77-9.

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