Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2015 | 1 |
2017 | 1 |
2022 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Hemophilia B: molecular pathogenesis and mutation analysis.
J Thromb Haemost. 2015 Jul;13(7):1184-95. doi: 10.1111/jth.12958. Epub 2015 May 18.
J Thromb Haemost. 2015.
PMID: 25851415
Free PMC article.
Review.
Hemophilia B results from several different mechanisms, and those associated with hemophilia B Leyden, ribosome readthrough of nonsense mutations and apparently 'silent' changes that do not alter amino acid coding are explored. ...
Hemophilia B results from several different mechanisms, and those associated with hemophilia B Leyden, ribosome readthr …
The Molecular Basis of FIX Deficiency in Hemophilia B.
Shen G, Gao M, Cao Q, Li W.
Shen G, et al.
Int J Mol Sci. 2022 Mar 2;23(5):2762. doi: 10.3390/ijms23052762.
Int J Mol Sci. 2022.
PMID: 35269902
Free PMC article.
Review.
Generally speaking, point mutations in the F9 promoter region result in hemophilia B Leyden, and those in the introns cause aberrant splicing. ...
Generally speaking, point mutations in the F9 promoter region result in hemophilia B Leyden, and those in the introns c …
Item in Clipboard
First case report of hemophilia B Leyden in Japan.
Yamashita A, Nagae C, Mori M, Ashikaga T, Kojima T, Taki M.
Yamashita A, et al.
Int J Hematol. 2017 Jul;106(1):135-137. doi: 10.1007/s12185-017-2194-4. Epub 2017 Feb 7.
Int J Hematol. 2017.
PMID: 28168417
Hemophilia B Leyden is a unique subtype of hemophilia B, characterized by increasing factor IX activity (FIX:C) after puberty and a lower normal range of FIX:C throughout adulthood. ...This mutation has been reported previously as the Leyden mutation. Althoug …
Hemophilia B Leyden is a unique subtype of hemophilia B, characterized by increasing factor IX activity (FIX:C) after p …
Item in Clipboard
Cite
Cite