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NATHAN HAWES, D.M.D.
D.M.D.
General Practice Dentistry
NPI: 1508285552Individual
Specialties, Licenses & Credentials
General Practice DentistryPrimary
Dentist — General Practice
Code: 1223G0001X
100189-15(WI)
Research & Publications (20)
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
Iris phenotypes and pigment dispersion caused by genes influencing pigmentation.
PMID 18715234·Pigment Cell Melanoma Res·2008
7-preclinical
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses.
PMID 18687716·J Physiol·2008
7-preclinical
Progressive morphological and functional defects in retinas from alpha1 integrin-null mice.
PMID 18614805·Invest Ophthalmol Vis Sci·2008
7-preclinical
AAV-mediated gene therapy for retinal degeneration in the rd10 mouse containing a recessive PDEbeta mutation.
PMID 18586879·Invest Ophthalmol Vis Sci·2008
7-preclinical
Dense nuclear cataract caused by the gammaB-crystallin S11R point mutation.
PMID 18172107·Invest Ophthalmol Vis Sci·2008
7-preclinical
Genetic background modifies inner ear and eye phenotypes of jag1 heterozygous mice.
PMID 17890364·Genetics·2007
7-preclinical
Restoration of cone vision in a mouse model of achromatopsia.
PMID 17515894·Nat Med·2007
7-preclinical
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
PMID 17267005·Vision Res·2007
7-preclinical
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.
PMID 17186464·Am J Hum Genet·2006
7-preclinical
Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2.
PMID 17065522·Invest Ophthalmol Vis Sci·2006
7-preclinical
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse.
PMID 16632484·Hum Mol Genet·2006
7-preclinical
Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice.
PMID 16595169·Genomics·2006
7-preclinical
Deficiency of SHP-1 protein-tyrosine phosphatase in "viable motheaten" mice results in retinal degeneration.
PMID 16505059·Invest Ophthalmol Vis Sci·2006
7-preclinical
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
PMID 15765048·Mol Vis·2005
7-preclinical
Replicated anterior zeugopod (raz): a polydactylous mouse mutant with lowered Shh signaling in the limb bud.
PMID 14597572·Development·2003
7-preclinical
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
PMID 14519688·Hum Mol Genet·2003
7-preclinical
Mouse model of subretinal neovascularization with choroidal anastomosis.
PMID 12972764·Retina·2003
7-preclinical
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.
PMID 12968670·J Bone Miner Res·2003
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1721 PROGRESSIVE PKWY
PLATTEVILLE, WI 53818 - Phone
- (608) 348-9591
Quick Facts
- NPI
- 1508285552
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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