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DR. ROBIN DAYANNA COLLIN D.O.
D.O.
Pediatrics Physician
NPI: 1255710315Individual
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
2019-01687(NC)
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
2019-01687(NC)
Research & Publications (20)
Amyloid-specific fluorophores for the rapid, sensitive in situ detection of prion contamination on surgical instruments.
PMID 17698675·J Gen Virol·2007
8-other
Molecular phylogenetic and embryological evidence that feeding larvae have been reacquired in a marine gastropod.
PMID 17438201·Biol Bull·2007
4-observational
The coding sequence of amyloid-beta precursor protein APP contains a neural-specific promoter element.
PMID 16626649·Brain Res·2006
4-observational
Sex ratio, life-history invariants, and patterns of sex change in a family of protandrous gastropods.
PMID 16739455·Evolution·2006
7-preclinical
Biosynthesis and differential processing of two pools of amyloid-beta precursor protein in a physiologically inducible neuroendocrine cell.
PMID 16092943·J Neurochem·2005
7-preclinical
The amyloid-beta precursor-like protein APLP2 and its relative APP are differentially regulated during neuroendocrine cell activation.
PMID 16154762·Mol Cell Neurosci·2005
7-preclinical
Identification and expression of the first nonmammalian amyloid-beta precursor-like protein APLP2 in the amphibian Xenopus laevis.
PMID 15128300·Eur J Biochem·2004
7-preclinical
Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1.
PMID 19548389·Ann Otol Rhinol Laryngol·2009
8-other
Early cure rates with narrow-margin slow-Mohs surgery for periocular malignant melanoma.
PMID 19076193·Dermatol Surg·2009
4-observational
Mutations in SPATA7 cause Leber congenital amaurosis and juvenile retinitis pigmentosa.
PMID 19268277·Am J Hum Genet·2009
7-preclinical
A rapid dual staining procedure for the quantitative discrimination of prion amyloid from tissues reveals how interactions between amyloid and lipids in tissue homogenates may hinder the detection of prions.
PMID 19318058·J Microbiol Methods·2009
7-preclinical
Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.
PMID 19615668·Am J Hum Genet·2009
8-other
A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.
PMID 19074807·Invest Ophthalmol Vis Sci·2009
8-other
Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3.
PMID 19372648·Audiol Neurootol·2009
8-other
Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.
PMID 19462854·Ann Otol Rhinol Laryngol·2009
8-other
Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear.
PMID 19005249·Audiol Neurootol·2009
8-other
Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer.
PMID 18575463·Eur J Hum Genet·2008
5-case
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 234 CROOKED CREEK PKWY STE 200
DURHAM, NC 27713 - Phone
- (919) 544-6644
Quick Facts
- NPI
- 1255710315
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 2
- Publications
- 20
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