R A Fridell
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Explore the profile of R A Fridell including associated specialties, affiliations and a list of published articles.
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27
Citations
1252
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Recent Articles
1.
Peters L, Fridell R, Boger E, San Agustin T, Madeo A, Griffith A, et al.
Clin Genet
. 2008 Feb;
73(4):367-72.
PMID: 18279434
We ascertained a large North American family, LMG2, segregating progressive, non-syndromic, sensorineural hearing loss. A genome-wide scan identified significant evidence for linkage (maximum logarithm of the odds (LOD) score =...
2.
Lloyd R, Vidal S, Jin L, Zhang S, Kovacs K, Horvath E, et al.
Am J Pathol
. 2001 Oct;
159(4):1375-82.
PMID: 11583965
The myosin superfamily of molecular motor proteins includes conventional myosins and several classes of unconventional myosins. Recent studies have characterized the human and mouse unconventional myosin XVA, which has a...
3.
Anderson D, Probst F, Belyantseva I, Fridell R, Beyer L, Martin D, et al.
Hum Mol Genet
. 2000 Aug;
9(12):1729-38.
PMID: 10915760
Recessive mutations in myosin 15, a class XV unconventional myosin, cause profound congenital deafness in humans and both deafness and vestibular dysfunction in mice homozygous for the shaker 2 and...
4.
Friedman T, Hinnant J, Fridell R, Wilcox E, Raphael Y, Camper S
Adv Otorhinolaryngol
. 2000 Jun;
56:131-44.
PMID: 10868225
No abstract available.
5.
Liang Y, Wang A, Belyantseva I, Anderson D, Probst F, Barber T, et al.
Genomics
. 1999 Nov;
61(3):243-58.
PMID: 10552926
Mutations in myosin XV are responsible for congenital profound deafness DFNB3 in humans and deafness and vestibular defects in shaker 2 mice. By combining direct cDNA analyses with a comparison...
6.
Truant R, Fridell R, Benson E, Herold A, Cullen B
Eur J Cell Biol
. 1999 Feb;
77(4):269-75.
PMID: 9930651
Protein nuclear import factors are not, in general, believed to function in the nuclear export of macromolecules and their reutilization therefore requires their recycling from the nucleus to the cytoplasm....
7.
Wang A, Liang Y, Fridell R, Probst F, Wilcox E, Touchman J, et al.
Science
. 1998 Jun;
280(5368):1447-51.
PMID: 9603736
DFNB3, a locus for nonsyndromic sensorineural recessive deafness, maps to a 3-centimorgan interval on human chromosome 17p11.2, a region that shows conserved synteny with mouse shaker-2. A human unconventional myosin...
8.
Probst F, Fridell R, Raphael Y, Saunders T, Wang A, Liang Y, et al.
Science
. 1998 Jun;
280(5368):1444-7.
PMID: 9603735
The shaker-2 mouse mutation, the homolog of human DFNB3, causes deafness and circling behavior. A bacterial artificial chromosome (BAC) transgene from the shaker-2 critical region corrected the vestibular defects, deafness,...
9.
Truant R, Fridell R, BENSON R, Bogerd H, Cullen B
Mol Cell Biol
. 1998 Mar;
18(3):1449-58.
PMID: 9488461
The nuclear import of proteins bearing a basic nuclear localization signal (NLS) is dependent on karyopherin alpha/importin alpha, which acts as the NLS receptor, and karyopherin beta1/importin beta, which binds...
10.
Bieniasz P, Fridell R, Anthony K, Cullen B
J Virol
. 1997 Sep;
71(9):7097-100.
PMID: 9261443
The human chemokine receptor hCXCR-4 serves as a coreceptor for T-cell-tropic (T-tropic) and dual-tropic strains of human immunodeficiency virus type 1 (HIV-1). We have isolated a homolog of hCXCR-4 from...