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Filters: Department: "Ophthalmology" Collection: "ir_uspace"
101 - 125 of 177
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TitleSetnameType
101 Molecular and developmental characterization of the heat shock cognate 4 gene of Drosophila melanogasterir_uspaceText
102 Molecular characterization of a third member of the guanylyl cyclase-activating protein subfamilyir_uspaceText
103 Molecular characterization of human and mouse photoreceptor guanylate cyclase-activating protein (GCAP) and chromosomal localization of the human geneir_uspaceText
104 Molecular phenotyping of retinal ganglion cellsir_uspaceText
105 Mouse opsin. Gene structure and molecular basis of multiple transcriptsir_uspaceText
106 Multiple components of surround modulation in primary visual cortex: Multiple neural circuits with multiple functions?ir_uspaceText
107 Mutant rhodopsin transgene expression on a null backgroundir_uspaceText
108 Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11qir_uspaceText
109 Neural interface for a cortical vision prosthesisir_uspaceText
110 Neural organization of the retina of the turtle Mauremys caspica: a light microscope and Golgi studyir_uspaceText
111 Neurologic conditions presenting as psychiatric disorders.ir_uspaceText
112 Neuronal interactions improve cortical population coding of movement directionir_uspaceText
113 Neurotransmitter properties of the newborn human retina.ir_uspaceText
114 New locus for autosomal dominant stargardt-like disease maps to chromosome 4ir_uspaceText
115 Noninvasive two-photon imaging reveals retinyl ester storage structures in the eyeir_uspaceText
116 Nonmydriatic fluorescence-based quantitative imaging of human macular pigment distributions.ir_uspaceText
117 Not so benign intracranial hypertension.ir_uspaceText
118 Novel GCAP1 missense mutation (L151F) in a large family with autosomal dominant cone-rod dystrophy (adCORD)ir_uspaceText
119 Novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degenerationir_uspaceText
120 Novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophyir_uspaceText
121 Nucleic acid vaccine encoding gD2 protects mice from herpes simplex virus type 2 disease.ir_uspaceText
122 Online parameter estimation in dynamic Markov Random Fields for image sequence analysisir_uspaceText
123 Oscillations in rod and horizontal cell membrane potential: evidence for feed-back to rods in the vertebrate retinair_uspaceText
124 Outbreak of toxic anterior segment syndrome following cataract surgery associated with impurities in autoclave steam moisture.ir_uspaceText
125 Penetrating keratoplasty for keratoconus: a long-term review of results and complicationsir_uspaceText
101 - 125 of 177