"Deoxyribonuclease HpaII" 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.
One of the Type II site-specific deoxyribonucleases (EC 3.1.21.4). It recognizes and cleaves the sequences C/CGG and GGC/C at the slash. HpaII is from Haemophilus parainfluenzae. Several isoschizomers have been identified. EC 3.1.21.-.
| Descriptor ID |
D019003
|
| MeSH Number(s) |
D08.811.150.280.260.420 D08.811.277.352.335.350.300.260.300 D08.811.277.352.355.325.300.260.300
|
| Concept/Terms |
Deoxyribonuclease HpaII- Deoxyribonuclease HpaII
- DNA Restriction Enzyme HpaII
- Endodeoxyribonuclease HpaII
- Endonuclease HpaII
|
Below are MeSH descriptors whose meaning is more general than "Deoxyribonuclease HpaII".
Below are MeSH descriptors whose meaning is more specific than "Deoxyribonuclease HpaII".
This graph shows the total number of publications written about "Deoxyribonuclease HpaII" by people in this website by year, and whether "Deoxyribonuclease HpaII" 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 |
|---|
| 1997 | 0 | 1 | 1 |
| 1998 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Deoxyribonuclease HpaII" by people in Profiles.
-
Hobson G, Stabley D, Funanage V, Marks H. A new polymorphism in the proteolipid protein (PLP1) gene and its use for carrier detection of PLP1 gene duplication in Pelizaeus-Merzbacher disease. Hum Mutat. 2001 Feb; 17(2):152.
-
Sukegawa K, Matsuzaki T, Fukuda S, Masuno M, Fukao T, Kokuryu M, Iwata S, Tomatsu S, Orii T, Kondo N. Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation. Clin Genet. 1998 Feb; 53(2):96-101.
-
Sukegawa K, Song XQ, Masuno M, Fukao T, Shimozawa N, Fukuda S, Isogai K, Nishio H, Matsuo M, Tomatsu S, Kondo N, Orii T. Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele. Hum Mutat. 1997; 10(5):361-7.
-
Naso MF, Morgan JL, Buchberg AM, Siracusa LD, Iozzo RV. Expression pattern and mapping of the murine versican gene (Cspg2) to chromosome 13. Genomics. 1995 Sep 01; 29(1):297-300.
-
Iwata H, Tomatsu S, Fukuda S, Uchiyama A, Rezvi GM, Ogawa T, Hori T, Nakashima Y, Yamagishi A, Sukegawa K, et al. Mucopolysaccharidosis IVA: polymorphic haplotypes and informative RFLPs in the Japanese population. Hum Genet. 1995 Mar; 95(3):257-64.
-
Adany R, Iozzo RV. Hypomethylation of the decorin proteoglycan gene in human colon cancer. Biochem J. 1991 Jun 01; 276 ( Pt 2):301-6.
-
Tomatsu S, Kobayashi Y, Fukumaki Y, Yubisui T, Orii T, Sakaki Y. The organization and the complete nucleotide sequence of the human NADH-cytochrome b5 reductase gene. Gene. 1989 Aug 15; 80(2):353-61.