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GARRETT YAM, MD
MD
Internal Medicine Physician
NPI: 1811146970Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
MD60078533(WA)
Pediatrics Physician
Pediatrics
Code: 208000000X
MD60078533(WA)
Research & Publications (20)
Correction of the disease phenotype of myocilin-causing glaucoma by a natural osmolyte.
PMID 19234343·Invest Ophthalmol Vis Sci·2009
8-other
Adipose-derived stem cells from pregnant women show higher proliferation rate unrelated to estrogen.
PMID 19181742·Hum Reprod·2009
8-other
Multiple gene polymorphisms analysis revealed a different profile of genetic polymorphisms of primary open-angle glaucoma in northern Chinese.
PMID 19145250·Mol Vis·2009
8-other
An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.
PMID 19503744·Mol Vis·2009
7-preclinical
A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.
PMID 19668596·Mol Vis·2009
8-other
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
PMID 18024964·Hum Mol Genet·2008
4-observational
Protein quality control: the who's who, the where's and therapeutic escapes.
PMID 18075753·Histochem Cell Biol·2008
6-review
Effect of topical Ginkgo biloba extract on steroid-induced changes in the trabecular meshwork and intraocular pressure.
PMID 19064852·Arch Ophthalmol·2008
7-preclinical
Association of CTLA-4 and IL-13 gene polymorphisms with Graves' disease and ophthalmopathy in Chinese children.
PMID 18296657·Invest Ophthalmol Vis Sci·2008
8-other
The cytotoxic and stress responses of human trabecular meshwork cells treated with triamcinolone acetonide.
PMID 18253094·Mol Vis·2008
8-other
Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset Fuchs endothelial corneal dystrophy.
PMID 18172091·Invest Ophthalmol Vis Sci·2008
8-other
Genotype phenotype analysis of Bietti's crystalline dystrophy in patients with CYP4V2 mutations.
PMID 17962476·Invest Ophthalmol Vis Sci·2007
8-other
A novel deletion variant of gammaD-crystallin responsible for congenital nuclear cataract.
PMID 18079686·Mol Vis·2007
8-other
Identification and functional characterization of a novel MYOC mutation in two primary open angle glaucoma families from The Netherlands.
PMID 17960117·Mol Vis·2007
5-case
4-Phenylbutyrate rescues trafficking incompetent mutant alpha-galactosidase A without restoring its functionality.
PMID 17592721·Biochem Biophys Res Commun·2007
7-preclinical
Sodium 4-phenylbutyrate acts as a chemical chaperone on misfolded myocilin to rescue cells from endoplasmic reticulum stress and apoptosis.
PMID 17389500·Invest Ophthalmol Vis Sci·2007
7-preclinical
Aggregated myocilin induces russell bodies and causes apoptosis: implications for the pathogenesis of myocilin-caused primary open-angle glaucoma.
PMID 17200186·Am J Pathol·2007
7-preclinical
Pharmacological chaperone corrects lysosomal storage in Fabry disease caused by trafficking-incompetent variants.
PMID 16531566·Am J Physiol Cell Physiol·2006
8-other
Multiple roles for the receptor tyrosine kinase axl in tumor formation.
PMID 16230391·Cancer Res·2005
7-preclinical
Critical role of the ubiquitin ligase activity of UHRF1, a nuclear RING finger protein, in tumor cell growth.
PMID 16195352·Mol Biol Cell·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2103 152ND AVE NE
REDMOND, WA 98052 - Phone
- (425) 746-2400
Quick Facts
- NPI
- 1811146970
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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