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.
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.
Below are MeSH descriptors whose meaning is more general than "Polymorphism, Restriction Fragment Length".
Below are MeSH descriptors whose meaning is more specific than "Polymorphism, Restriction Fragment Length".
This graph shows the total number of publications written about "Polymorphism, Restriction Fragment Length" by people in Harvard Catalyst Profiles by year, and whether "Polymorphism, Restriction Fragment Length" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1994 | 3 | 23 | 26 |
| 1995 | 1 | 12 | 13 |
| 1996 | 1 | 19 | 20 |
| 1997 | 3 | 10 | 13 |
| 1998 | 2 | 7 | 9 |
| 1999 | 2 | 20 | 22 |
| 2000 | 0 | 13 | 13 |
| 2001 | 3 | 18 | 21 |
| 2002 | 2 | 19 | 21 |
| 2003 | 3 | 23 | 26 |
| 2004 | 2 | 12 | 14 |
| 2005 | 0 | 13 | 13 |
| 2006 | 2 | 8 | 10 |
| 2007 | 0 | 5 | 5 |
| 2008 | 1 | 3 | 4 |
| 2009 | 1 | 5 | 6 |
| 2010 | 0 | 9 | 9 |
| 2011 | 0 | 4 | 4 |
| 2012 | 0 | 2 | 2 |
| 2013 | 0 | 6 | 6 |
| 2014 | 1 | 0 | 1 |
| 2015 | 0 | 3 | 3 |
| 2016 | 1 | 5 | 6 |
| 2017 | 0 | 2 | 2 |
| 2019 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
Below are the most recent publications written about "Polymorphism, Restriction Fragment Length" by people in Profiles.
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Homozygosity mapping: a game-changer for autosomal recessive diseases. Nat Rev Genet. 2022 01; 23(1):2-3.
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Automated typing of red blood cell and platelet antigens from whole exome sequences. Transfusion. 2019 10; 59(10):3253-3263.
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Association between Fc? receptor IIA, IIIA and IIIB genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya. BMC Infect Dis. 2017 04 20; 17(1):289.
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High resolution melting: a useful field-deployable method to measure dhfr and dhps drug resistance in both highly and lowly endemic Plasmodium populations. Malar J. 2017 Apr 19; 16(1):153.
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In Vitro Corticogenesis from Embryonic Stem Cells Recapitulates the In Vivo Epigenetic Control of Imprinted Gene Expression. Cereb Cortex. 2017 03 01; 27(3):2418-2433.
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Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia. J Clin Densitom. 2018 Apr - Jun; 21(2):205-212.
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Molecular characterization of cryptosporidium in children aged 0- 5 years with diarrhea in Jos, Nigeria. Pan Afr Med J. 2016; 25:253.
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Exploring genotype concordance in epidemiologically linked cases of tuberculosis in New York City. Epidemiol Infect. 2017 02; 145(3):503-514.
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Hepatitis B virus genotypes among chronic hepatitis B patients reporting at Korle-Bu teaching hospital, Accra, Ghana. Pan Afr Med J. 2016; 25(Suppl 1):5.
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[Study of genetic variants in the BDNF, COMT, DAT1 and SERT genes in Colombian children with attention deficit disorder]. Rev Colomb Psiquiatr. 2017 Oct - Dec; 46(4):222-228.