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RAMCHANDRA RAO AYYAGARI, M.D.
M.D.
Reproductive Endocrinology Physician
NPI: 1942230644Individual
Specialties, Licenses & Credentials
Reproductive Endocrinology PhysicianPrimary
Obstetrics & Gynecology — Reproductive Endocrinology
Code: 207VE0102X
A42495(CA)CA42495(CA)
Research & Publications (20)
A novel rat model with obesity-associated retinal degeneration.
PMID 19369235·Invest Ophthalmol Vis Sci·2009
7-preclinical
Erythrocyte aldose reductase activity and sorbitol levels in diabetic retinopathy.
PMID 18385795·Mol Vis·2008
4-observational
Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene.
PMID 18805803·Hum Mol Genet·2008
4-observational
Possible association between long anterior lens zonules and plateau iris configuration.
PMID 18703950·J Glaucoma·2008
5-case
Molecular and phenotypic analysis of a family with autosomal recessive cone-rod dystrophy and Stargardt disease.
PMID 17893657·Mol Vis·2007
8-other
Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death.
PMID 17208947·Hum Mol Genet·2007
7-preclinical
Molecular testing for hereditary retinal disease as part of clinical care.
PMID 17296903·Arch Ophthalmol·2007
5-case
An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation.
PMID 16884758·Vision Res·2006
5-case
Complement factor H: spatial and temporal expression and localization in the eye.
PMID 16936129·Invest Ophthalmol Vis Sci·2006
7-preclinical
Projecting absolute invasive breast cancer risk in white women with a model that includes mammographic density.
PMID 16954474·J Natl Cancer Inst·2006
8-other
Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration.
PMID 17003453·Invest Ophthalmol Vis Sci·2006
7-preclinical
Spatial and temporal expression of MFRP and its interaction with CTRP5.
PMID 17122143·Invest Ophthalmol Vis Sci·2006
7-preclinical
Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease.
PMID 16877435·Invest Ophthalmol Vis Sci·2006
7-preclinical
CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretion.
PMID 17122142·Invest Ophthalmol Vis Sci·2006
7-preclinical
Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform.
PMID 16123440·Invest Ophthalmol Vis Sci·2005
8-other
Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation.
PMID 16123441·Invest Ophthalmol Vis Sci·2005
8-other
Stargardt-like macular dystrophy protein ELOVL4 exerts a dominant negative effect by recruiting wild-type protein into aggresomes.
PMID 16163264·Mol Vis·2005
7-preclinical
Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.
PMID 16189710·Hum Genet·2005
8-other
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
PMID 16252232·Am J Hum Genet·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
- 3535 SAN DIMAS ST, SUITE 20
BAKERSFIELD, CA 93301 - Phone
- (661) 323-3266
Quick Facts
- NPI
- 1942230644
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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