Heidi M Stricker
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Explore the profile of Heidi M Stricker including associated specialties, affiliations and a list of published articles.
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5
Citations
172
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Recent Articles
1.
Conley S, Stricker H, Naash M
Biochemistry
. 2010 Jan;
49(5):905-11.
PMID: 20055437
Mutations in the protein product of the retinal degeneration slow (RDS) gene cause both rod-dominant retinitis pigmentosa and different forms of cone-dominant macular dystrophies. In particular, mutations in codon 244...
2.
Gou D, Mishra A, Weng T, Su L, Chintagari N, Wang Z, et al.
J Biol Chem
. 2008 Mar;
283(19):13156-64.
PMID: 18332131
Annexin A2, a calcium-dependent phospholipid-binding protein, is abundantly expressed in alveolar type II cells where it plays a role in lung surfactant secretion. Nevertheless, little is known about the details...
3.
Wang Y, Stricker H, Gou D, Liu L
Front Biosci
. 2006 Nov;
12:2316-29.
PMID: 17127242
MicroRNAs (miRNAs) are approximately 22 nucleotide (nt) non-coding RNAs that participate in gene regulation. MiRNAs confer their regulation at a post-transcriptional level, where they either cleave or repress translation of...
4.
Ding X, Stricker H, Naash M
Biochemistry
. 2005 Mar;
44(12):4897-904.
PMID: 15779916
Peripherin/rds (P/rds) is a disk rim protein that assembles into homo and hetero complexes with its nonglycosylated homologue, Rom-1, to maintain the integrity of the photoreceptor outer segment. Mutations in...
5.
Stricker H, Ding X, Quiambao A, Fliesler S, Naash M
Biochem J
. 2005 Jan;
388(Pt 2):605-13.
PMID: 15656787
P/rds (peripherin/retinal degeneration slow) is a photoreceptor-specific membrane glycoprotein necessary for outer segment disc morphogenesis. Mutations in P/rds are associated with different blinding diseases. A C214S (Cys214-->Ser) missense mutation has...