-
1
-
-
69549107648
-
Challenges in quantifying multisensory integration: Alternative criteria, models, and inverse effectiveness
-
Stein BE, Stanford TR, Ramachandran R, Perrault TJ Jr, Rowland BA. 2009. Challenges in quantifying multisensory integration: alternative criteria, models, and inverse effectiveness. Exp. Brain Res. 198: 113-26
-
(2009)
Exp. Brain Res.
, vol.198
, pp. 113-126
-
-
Stein, B.E.1
Stanford, T.R.2
Ramachandran, R.3
Perrault Jr., T.J.4
Rowland, B.A.5
-
2
-
-
0014517607
-
Visual area of the lateral suprasylvian gyrus (Clare-Bishop area) of the cat
-
Hubel DH, Wiesel TN. 1969. Visual area of the lateral suprasylvian gyrus (Clare-Bishop area) of the cat. J. Physiol. 202:251-60
-
(1969)
J. Physiol.
, vol.202
, pp. 251-260
-
-
Hubel, D.H.1
Wiesel, T.N.2
-
3
-
-
47749090524
-
Use of alternative animals as asthma models
-
Kirschvink N, Reinhold P. 2008. Use of alternative animals as asthma models. Curr. Drug Targets 9:470-84
-
(2008)
Curr. Drug Targets
, vol.9
, pp. 470-484
-
-
Kirschvink, N.1
Reinhold, P.2
-
4
-
-
84862284235
-
Parallels in sources of trauma, pain, distress, and suffering in humans and nonhuman animals
-
Ferdowsian H, Merskin D. 2012. Parallels in sources of trauma, pain, distress, and suffering in humans and nonhuman animals. J. Trauma Dissoc. 13:448-68
-
(2012)
J. Trauma Dissoc.
, vol.13
, pp. 448-468
-
-
Ferdowsian, H.1
Merskin, D.2
-
5
-
-
79956132341
-
Fetal alcohol spectrum disorders and abnormal neuronal plasticity
-
Medina AE. 2011. Fetal alcohol spectrum disorders and abnormal neuronal plasticity. Neuroscientist 17: 274-87
-
(2011)
Neuroscientist
, vol.17
, pp. 274-287
-
-
Medina, A.E.1
-
6
-
-
58049202870
-
Fixational eye movements across vertebrates: Comparative dynamics, physiology, and perception
-
Martinez-Conde S, Macknik SL. 2008. Fixational eye movements across vertebrates: comparative dynamics, physiology, and perception. J. Vis. 8:1-16
-
(2008)
J. Vis.
, vol.8
, pp. 1-16
-
-
Martinez-Conde, S.1
MacKnik, S.L.2
-
7
-
-
34548356698
-
Mutation in CEP290 discovered for cat model of human retinal degeneration
-
Menotti-Raymond M, David VA, Schäffer AA, Stephens R, Wells D, et al. 2007. Mutation in CEP290 discovered for cat model of human retinal degeneration. J. Hered. 98:211-20
-
(2007)
J. Hered.
, vol.98
, pp. 211-220
-
-
Menotti-Raymond, M.1
David, V.A.2
Schäffer, A.A.3
Stephens, R.4
Wells, D.5
-
8
-
-
77953267163
-
Mutation discovered in a feline model of human congenital retinal blinding disease
-
Menotti-Raymond M, Deckman KH, David V, Myrkalo J, O'Brien SJ, Narfström K. 2010. Mutation discovered in a feline model of human congenital retinal blinding disease. Investig. Ophthalmol. Vis. Sci. 51:2852-59
-
(2010)
Investig. Ophthalmol. Vis. Sci.
, vol.51
, pp. 2852-2859
-
-
Menotti-Raymond, M.1
Deckman, K.H.2
David, V.3
Myrkalo, J.4
O'Brien, S.J.5
Narfström, K.6
-
9
-
-
85081814567
-
Candidate gene analysis of a feline model of primary congenital glaucoma implicates LTBP2 as the causative locus
-
Ellinwood NM, Deckman KH, Zhao Z, Rutz-Mendicino MM, Jens JK, et al. 2010. Candidate gene analysis of a feline model of primary congenital glaucoma implicates LTBP2 as the causative locus. In Assoc. Res. Vis. Ophthalmol. Annu. Meet. Abstr. 6390
-
(2010)
Assoc. Res. Vis. Ophthalmol. Annu. Meet. Abstr. 6390
-
-
Ellinwood, N.M.1
Deckman, K.H.2
Zhao, Z.3
Rutz-Mendicino, M.M.4
Jens, J.K.5
-
10
-
-
41949128427
-
Functional and structural changes in the retina of wirehaired dachshunds with early onset cone-rod dystrophy
-
Ropstad EO, Narfström K, Lingaas F, Wiik C, Bruun A, Bjerkås E. 2008. Functional and structural changes in the retina of wirehaired dachshunds with early onset cone-rod dystrophy. Investig. Ophthalmol. Vis. Sci. 49(3):1106-15
-
(2008)
Investig. Ophthalmol. Vis. Sci.
, vol.49
, Issue.3
, pp. 1106-1115
-
-
Ropstad, E.O.1
Narfström, K.2
Lingaas, F.3
Wiik, C.4
Bruun, A.5
Bjerkås, E.6
-
11
-
-
20444431845
-
Early-onset, autosomal recessive, progressive retinal atrophy in Persian cats
-
Rah H, Maggs DJ, Blankenship TN, Narfström K, Lyons LA. 2005. Early-onset, autosomal recessive, progressive retinal atrophy in Persian cats. Investig. Ophthalmol. Vis. Sci. 46:1742-47
-
(2005)
Investig. Ophthalmol. Vis. Sci.
, vol.46
, pp. 1742-1747
-
-
Rah, H.1
Maggs, D.J.2
Blankenship, T.N.3
Narfström, K.4
Lyons, L.A.5
-
12
-
-
36048982458
-
Initial sequence and comparative analysis of the cat genome
-
Pontius JU, Mullikin JC, Smith DR, Team AS, Lindblad-Toh K, et al. 2007. Initial sequence and comparative analysis of the cat genome. Genome Res. 17:1675-89
-
(2007)
Genome Res.
, vol.17
, pp. 1675-1689
-
-
Pontius, J.U.1
Mullikin, J.C.2
Smith, D.R.3
Lindblad-Toh, K.4
-
13
-
-
34548451579
-
Genome annotation resource fields-GARFIELD: A genome browser for Felis catus
-
Pontius JU, O'Brien SJ. 2007. Genome annotation resource fields-GARFIELD: A genome browser for Felis catus. J. Hered. 98:386-89
-
(2007)
J. Hered.
, vol.98
, pp. 386-389
-
-
Pontius, J.U.1
O'Brien, S.J.2
-
14
-
-
77955165253
-
Light whole genome sequence for SNP discovery across domestic cat breeds
-
Mullikin JC, Hansen NF, Shen L, Ebling H, Donahue WF, et al. 2010. Light whole genome sequence for SNP discovery across domestic cat breeds. BMC Genomics 11:406
-
(2010)
BMC Genomics
, vol.11
, pp. 406
-
-
Mullikin, J.C.1
Hansen, N.F.2
Shen, L.3
Ebling, H.4
Donahue, W.F.5
-
15
-
-
61849170302
-
A high-resolution cat radiation hybrid and integrated FISH mapping resource for phylogenomic studies across Felidae
-
Davis BW, Raudsepp T, Pearks Wilkerson AJ, Agarwala R, Schäffer AA, et al. 2009. A high-resolution cat radiation hybrid and integrated FISH mapping resource for phylogenomic studies across Felidae. Genomics 93:299-304
-
(2009)
Genomics
, vol.93
, pp. 299-304
-
-
Davis, B.W.1
Raudsepp, T.2
Pearks Wilkerson, A.J.3
Agarwala, R.4
Schäffer, A.A.5
-
16
-
-
61849163371
-
An autosomal genetic linkage map of the domestic cat, Felis silvestris catus
-
Menotti-Raymond M, David VA, Schäffer AA, Tomlin JF, Eizirik E, et al. 2009. An autosomal genetic linkage map of the domestic cat, Felis silvestris catus. Genomics 93:305-13
-
(2009)
Genomics
, vol.93
, pp. 305-313
-
-
Menotti-Raymond, M.1
David, V.A.2
Schäffer, A.A.3
Tomlin, J.F.4
Eizirik, E.5
-
17
-
-
0002718955
-
Ophthalmic anatomy
-
ed. KN Gelatt Ames, IA: Blackwell
-
Samuelson DA. 2007. Ophthalmic anatomy. In Veterinary Ophthalmology, ed. KN Gelatt, pp. 46-47. Ames, IA: Blackwell
-
(2007)
Veterinary Ophthalmology
, pp. 46-47
-
-
Samuelson, D.A.1
-
18
-
-
80052929549
-
Feline glaucoma-a comprehensive review
-
McLellan GJ, Miller PE. 2011. Feline glaucoma-a comprehensive review. Vet. Ophthalmol. 14(Suppl. 1):15-29
-
(2011)
Vet. Ophthalmol.
, vol.14
, Issue.SUPPL. 1
, pp. 15-29
-
-
McLellan, G.J.1
Miller, P.E.2
-
20
-
-
0015146723
-
Ultrastructure of the exit pathway of the aqueous in lower mammals. (A preliminary report on the "angular aqueous plexus")
-
Tripathi RC. 1971. Ultrastructure of the exit pathway of the aqueous in lower mammals. (A preliminary report on the "angular aqueous plexus"). Exp. Eye Res. 12:311-14
-
(1971)
Exp. Eye Res.
, vol.12
, pp. 311-314
-
-
Tripathi, R.C.1
-
21
-
-
0015924607
-
The distribution of rods and cones in the retina of the cat (Felis domesticus)
-
Steinberg RH, Reid M, Lacy PL. 1973. The distribution of rods and cones in the retina of the cat (Felis domesticus). J. Comp. Neurol. 148:229-48
-
(1973)
J. Comp. Neurol.
, vol.148
, pp. 229-248
-
-
Steinberg, R.H.1
Reid, M.2
Lacy, P.L.3
-
22
-
-
0013784647
-
A quantitative analysis of the distribution of ganglion cells in the cat's retina
-
Stone J. 1965. A quantitative analysis of the distribution of ganglion cells in the cat's retina. J. Comp. Neurol. 124:337-52
-
(1965)
J. Comp. Neurol.
, vol.124
, pp. 337-352
-
-
Stone, J.1
-
23
-
-
0021944021
-
Progressive retinal atrophy in the Abyssinian cat clinical characteristics
-
Narfström K. 1985. Progressive retinal atrophy in the Abyssinian cat. Clinical characteristics. Investig. Ophthalmol. Vis. Sci. 26:193-200
-
(1985)
Investig. Ophthalmol. Vis. Sci.
, vol.26
, pp. 193-200
-
-
Narfström, K.1
-
24
-
-
44649150165
-
Some quantitative aspects of the cat's eye: Axis and plane of reference, visual field co-ordinates and optics
-
Bishop PO, Kozak W, Vakkur GJ. 1962. Some quantitative aspects of the cat's eye: axis and plane of reference, visual field co-ordinates and optics. J. Physiol. 163:466-502
-
(1962)
J. Physiol.
, vol.163
, pp. 466-502
-
-
Bishop, P.O.1
Kozak, W.2
Vakkur, G.J.3
-
25
-
-
0018213840
-
Postnatal development of the cat retina. A qualitative and quantitative electron microscopy study
-
Vogel M, Haug H. 1978. Postnatal development of the cat retina. A qualitative and quantitative electron microscopy study. Verh. Anat. Ges. 1978:327-29
-
(1978)
Verh. Anat. Ges.
, vol.1978
, pp. 327-329
-
-
Vogel, M.1
Haug, H.2
-
26
-
-
0018189317
-
Postnatal development of the cat's retina: A concept of maturation obtained by qualitative and quantitative examination
-
VogelM. 1978. Postnatal development of the cat's retina: A concept of maturation obtained by qualitative and quantitative examination. Albrecht Graefes Arch. Klin. Exp. Ophthalmol. 208:93-107
-
(1978)
Albrecht Graefes Arch. Klin. Exp. Ophthalmol.
, vol.208
, pp. 93-107
-
-
Vogel, M.1
-
27
-
-
0018651574
-
Anatomic and physiologic development of the photoreceptor of the kitten
-
Tucker GS, Hamasaki DI, Labbie A, Muroff J. 1979. Anatomic and physiologic development of the photoreceptor of the kitten. Exp. Brain Res. 37:459-74
-
(1979)
Exp. Brain Res.
, vol.37
, pp. 459-474
-
-
Tucker, G.S.1
Hamasaki, D.I.2
Labbie, A.3
Muroff, J.4
-
28
-
-
0001769182
-
Ocular embryology and congenital malformation
-
ed. KN Gelatt Ames, IA: Blackwell
-
Cook CS. 2007. Ocular embryology and congenital malformation. In Veterinary Ophthalmology, ed. KN Gelatt, pp. 3-30. Ames, IA: Blackwell
-
(2007)
Veterinary Ophthalmology
, pp. 3-30
-
-
Cook, C.S.1
-
29
-
-
0023692917
-
Developmental studies using clinical electroretinography
-
Narfström K, Wilen M, Andersson BE. 1988. Developmental studies using clinical electroretinography. Doc. Ophthalmol. 89:111-18
-
(1988)
Doc. Ophthalmol.
, vol.89
, pp. 111-118
-
-
Narfström, K.1
Wilen, M.2
Andersson, B.E.3
-
30
-
-
84906257348
-
Cone and rod electroretinograms during development in the cat
-
Ikeda H, Jacobson SG. 1982. Cone and rod electroretinograms during development in the cat. J. Physiol. 329:21-22
-
(1982)
J. Physiol.
, vol.329
, pp. 21-22
-
-
Ikeda, H.1
Jacobson, S.G.2
-
31
-
-
0344923040
-
Some properties of components of the cat electroretinogram revealed by local recording under oil
-
Arden GB, Brown KT. 1965. Some properties of components of the cat electroretinogram revealed by local recording under oil. J. Physiol. 176:429-61
-
(1965)
J. Physiol.
, vol.176
, pp. 429-461
-
-
Arden, G.B.1
Brown, K.T.2
-
32
-
-
0004385207
-
Analysis of the intraretinal electroretinogram in the intact cat eye
-
Brown KT, Wiesel TN. 1961. Analysis of the intraretinal electroretinogram in the intact cat eye. J. Physiol. 158:229-56
-
(1961)
J. Physiol.
, vol.158
, pp. 229-256
-
-
Brown, K.T.1
Wiesel, T.N.2
-
33
-
-
0032323525
-
Dissecting the dark-adapted electroretinogram
-
Robson JG, Frishman LJ. 1998. Dissecting the dark-adapted electroretinogram. Doc. Ophthalmol. 95: 187-215
-
(1998)
Doc. Ophthalmol.
, vol.95
, pp. 187-215
-
-
Robson, J.G.1
Frishman, L.J.2
-
34
-
-
0033165989
-
The contributions of voltage-and time-dependent potassium conductances to the electroretinogram in rabbits
-
Lei B, Perlman I. 1999. The contributions of voltage-and time-dependent potassium conductances to the electroretinogram in rabbits. Vis. Neurosci. 16:743-54
-
(1999)
Vis. Neurosci.
, vol.16
, pp. 743-754
-
-
Lei, B.1
Perlman, I.2
-
35
-
-
0014949212
-
Intracellular responses to light from cat pigment epithelium: Origin of the electroretinogram c-wave
-
Steinberg RH, Schmidt R, Brown KT. 1970. Intracellular responses to light from cat pigment epithelium: origin of the electroretinogram c-wave. Nature 227:728-30
-
(1970)
Nature
, vol.227
, pp. 728-730
-
-
Steinberg, R.H.1
Schmidt, R.2
Brown, K.T.3
-
36
-
-
18144379141
-
Congenital and hereditary ocular abnormalities in cats
-
Glaze MB. 2005. Congenital and hereditary ocular abnormalities in cats. Clin. Tech. Small Anim. Pract. 20:74-82
-
(2005)
Clin. Tech. Small Anim. Pract.
, vol.20
, pp. 74-82
-
-
Glaze, M.B.1
-
37
-
-
0032790491
-
Identification and characterization of the molecular lesion causing mucopolysaccharidosis type i in cats
-
He X, Li CM, Simonaro CM, Wan Q, Haskins ME, et al. 1999. Identification and characterization of the molecular lesion causing mucopolysaccharidosis type I in cats. Mol. Genet. Metab. 67:106-12
-
(1999)
Mol. Genet. Metab.
, vol.67
, pp. 106-112
-
-
He, X.1
Li, C.M.2
Simonaro, C.M.3
Wan, Q.4
Haskins, M.E.5
-
39
-
-
0020563454
-
The pathology of the feline model of mucopolysaccharidosis i
-
Haskins ME, Aguirre GD, Jezyk PF, Desnick RJ, Patterson DF. 1983. The pathology of the feline model of mucopolysaccharidosis I. Am. J. Pathol. 112:27-36
-
(1983)
Am. J. Pathol.
, vol.112
, pp. 27-36
-
-
Haskins, M.E.1
Aguirre, G.D.2
Jezyk, P.F.3
Desnick, R.J.4
Patterson, D.F.5
-
40
-
-
0017758232
-
Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: A model of Maroteaux-Lamy syndrome
-
Jezyk PF, Haskins ME, Patterson DF, Mellman WJ, Greenstein M. 1977. Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome. Science 198:834-36
-
(1977)
Science
, vol.198
, pp. 834-836
-
-
Jezyk, P.F.1
Haskins, M.E.2
Patterson, D.F.3
Mellman, W.J.4
Greenstein, M.5
-
41
-
-
0019637466
-
Animal model of human disease: Mucopolysaccharidosis VIMaroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese cat
-
Haskins ME, Jezyk PF, Desnick RJ, Patterson DF. 1981. Animal model of human disease: Mucopolysaccharidosis VIMaroteaux-Lamy syndrome, Arylsulfatase B-deficient mucopolysaccharidosis in the Siamese cat. Am. J. Pathol. 105:191-93
-
(1981)
Am. J. Pathol.
, vol.105
, pp. 191-193
-
-
Haskins, M.E.1
Jezyk, P.F.2
Desnick, R.J.3
Patterson, D.F.4
-
42
-
-
0029998538
-
Feline mucopolysaccharidosis type VI. Characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the disease
-
Yogalingam G, Litjens T, Bielicki J, Crawley AC, Muller V, et al. 1996. Feline mucopolysaccharidosis type VI. Characterization of recombinant N-acetylgalactosamine 4-sulfatase and identification of a mutation causing the disease. J. Biol. Chem. 271:27259-65
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 27259-27265
-
-
Yogalingam, G.1
Litjens, T.2
Bielicki, J.3
Crawley, A.C.4
Muller, V.5
-
43
-
-
0031985352
-
Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes
-
Crawley AC, Yogalingam G, Muller VJ, Hopwood JJ. 1998. Two mutations within a feline mucopolysaccharidosis type VI colony cause three different clinical phenotypes. J. Clin. Investig. 101:109-19
-
(1998)
J. Clin. Investig.
, vol.101
, pp. 109-119
-
-
Crawley, A.C.1
Yogalingam, G.2
Muller, V.J.3
Hopwood, J.J.4
-
44
-
-
0042385114
-
Prevalence of mucopolysaccharidosis type VI mutations in Siamese cats
-
Crawley AC, Muntz FH, Haskins ME, Jones BR, Hopwood JJ. 2003. Prevalence of mucopolysaccharidosis type VI mutations in Siamese cats. J. Vet. Int. Med. Am. Coll. Vet. Int. Med. 17:495-98
-
(2003)
J. Vet. Int. Med. Am. Coll. Vet. Int. Med.
, vol.17
, pp. 495-498
-
-
Crawley, A.C.1
Muntz, F.H.2
Haskins, M.E.3
Jones, B.R.4
Hopwood, J.J.5
-
45
-
-
14044270228
-
Phenotypic rescue after adenoassociated virus-mediated delivery of 4-sulfatase to the retinal pigment epithelium of feline mucopolysaccharidosis VI
-
Ho TT, Maguire AM, Aguirre GD, Surace EM, Anand V, et al. 2002. Phenotypic rescue after adenoassociated virus-mediated delivery of 4-sulfatase to the retinal pigment epithelium of feline mucopolysaccharidosis VI. J. Gene Med. 4:613-21
-
(2002)
J. Gene Med.
, vol.4
, pp. 613-621
-
-
Ho, T.T.1
Maguire, A.M.2
Aguirre, G.D.3
Surace, E.M.4
Anand, V.5
-
46
-
-
0028473064
-
Feline mucopolysaccharidosis VII due to beta-glucuronidase deficiency
-
Gitzelmann R, Bosshard NU, Superti-Furga A, Spycher MA, Briner J, et al. 1994. Feline mucopolysaccharidosis VII due to beta-glucuronidase deficiency. Vet. Pathol. 31:435-43
-
(1994)
Vet. Pathol.
, vol.31
, pp. 435-443
-
-
Gitzelmann, R.1
Bosshard, N.U.2
Superti-Furga, A.3
Spycher, M.A.4
Briner, J.5
-
47
-
-
0033153522
-
Molecular basis of feline betaglucuronidase deficiency: An animal model of mucopolysaccharidosis VII
-
Fyfe JC, Kurzhals RL, Lassaline ME, Henthorn PS, Alur PR, et al. 1999. Molecular basis of feline betaglucuronidase deficiency: an animal model of mucopolysaccharidosis VII. Genomics 58:121-28
-
(1999)
Genomics
, vol.58
, pp. 121-128
-
-
Fyfe, J.C.1
Kurzhals, R.L.2
Lassaline, M.E.3
Henthorn, P.S.4
Alur, P.R.5
-
48
-
-
0019162037
-
Biochemical studies on a case of feline mannosidosis
-
Burditt LJ, Chotai K, Hirani S, Nugent PG, Winchester BG, BlakemoreWF. 1980. Biochemical studies on a case of feline mannosidosis. Biochem. J. 189:467-73
-
(1980)
Biochem. J.
, vol.189
, pp. 467-473
-
-
Burditt, L.J.1
Chotai, K.2
Hirani, S.3
Nugent, P.G.4
Winchester, B.G.5
Blakemore, W.F.6
-
49
-
-
0031453268
-
Purification of feline lysosomal alphamannosidase, determination of its cDNA sequence and identification of a mutation causing alphamannosidosis in Persian cats
-
Berg T, Tollersrud OK, Walkley SU, Siegel D, Nilssen O. 1997. Purification of feline lysosomal alphamannosidase, determination of its cDNA sequence and identification of a mutation causing alphamannosidosis in Persian cats. Biochem. J. 328:863-70
-
(1997)
Biochem. J.
, vol.328
, pp. 863-870
-
-
Berg, T.1
Tollersrud, O.K.2
Walkley, S.U.3
Siegel, D.4
Nilssen, O.5
-
50
-
-
0024097967
-
The clinical and pathologic heterogeneity of feline alpha-mannosidosis
-
Cummings JF, Wood PA, de Lahunta A, Walkley SU, Le Boeuf L. 1988. The clinical and pathologic heterogeneity of feline alpha-mannosidosis. J. Vet. Int. Med. Am. Coll. Vet. Int. Med. 2:163-70
-
(1988)
J. Vet. Int. Med. Am. Coll. Vet. Int. Med.
, vol.2
, pp. 163-170
-
-
Cummings, J.F.1
Wood, P.A.2
De Lahunta, A.3
Walkley, S.U.4
Le Boeuf, L.5
-
51
-
-
0031710552
-
Beta-galactosidase deficiency in a Korat cat: A new form of feline GM1-gangliosidosis
-
De Maria R, Divari S, Bo S, Sonnio S, Lotti D, et al. 1998. Beta-galactosidase deficiency in a Korat cat: a new form of feline GM1-gangliosidosis. Acta Neuropathol. 96:307-14
-
(1998)
Acta Neuropathol.
, vol.96
, pp. 307-314
-
-
De Maria, R.1
Divari, S.2
Bo, S.3
Sonnio, S.4
Lotti, D.5
-
52
-
-
0015146931
-
NeuronalGM1 gangliosidosis in a Siamese cat with b-galactosidase deficiency
-
Baker HJ Jr, Lindsey JR, McKhannGM,Farrell DF. 1971. NeuronalGM1 gangliosidosis in a Siamese cat with b-galactosidase deficiency. Science 174:838-39
-
(1971)
Science
, vol.174
, pp. 838-839
-
-
Baker Jr., H.J.1
Lindsey, J.R.2
McKhann, G.M.3
Farrell, D.F.4
-
53
-
-
43249114793
-
Molecular consequences of the pathogenic mutation in feline G M1) gangliosidosis
-
Martin DR, Rigat BA, Foureman P, Varadarajan GS, Hwang M, et al. 2008. Molecular consequences of the pathogenic mutation in feline G(M1) gangliosidosis. Mol. Genet. Metab. 94:212-21
-
(2008)
Mol. Genet. Metab.
, vol.94
, pp. 212-221
-
-
Martin, D.R.1
Rigat, B.A.2
Foureman, P.3
Varadarajan, G.S.4
Hwang, M.5
-
55
-
-
0021919599
-
Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats
-
Neuwelt EA, Johnson WG, Blank NK, Pagel MA,Maslen-McClure C, et al. 1985. Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats. J. Clin. Investig. 76:482-90
-
(1985)
J. Clin. Investig.
, vol.76
, pp. 482-490
-
-
Neuwelt, E.A.1
Johnson, W.G.2
Blank, N.K.3
Pagel Mamaslen-Mcclure, C.4
-
56
-
-
27944484472
-
Mutation of theGM2activator protein in a feline model of GM2 gangliosidosis
-
Martin DR, Cox NR, Morrison NE, KennamerDM,Peck SL, et al. 2005. Mutation of theGM2activator protein in a feline model of GM2 gangliosidosis. Acta Neuropathol. 110:443-50
-
(2005)
Acta Neuropathol.
, vol.110
, pp. 443-450
-
-
Martin, D.R.1
Cox, N.R.2
Morrison, N.E.3
Kennamer, D.M.4
Peck, S.L.5
-
57
-
-
1842714246
-
Aninversion of 25 base pairs causes feline GM2 gangliosidosis variant
-
Martin DR, Krum BK, Varadarajan GS, Hathcock TL, Smith BF, Baker HJ. 2004.Aninversion of 25 base pairs causes feline GM2 gangliosidosis variant. Exp. Neurol. 187:30-37
-
(2004)
Exp. Neurol.
, vol.187
, pp. 30-37
-
-
Martin, D.R.1
Krum, B.K.2
Varadarajan, G.S.3
Hathcock, T.L.4
Smith, B.F.5
Baker, H.J.6
-
58
-
-
0028336694
-
Characterization of the molecular defect in a feline model for type II GM2-gangliosidosis (Sandhoff disease)
-
Muldoon LL, Neuwelt EA, Pagel MA, Weiss DL. 1994. Characterization of the molecular defect in a feline model for type II GM2-gangliosidosis (Sandhoff disease). Am. J. Pathol. 144:1109-18
-
(1994)
Am. J. Pathol.
, vol.144
, pp. 1109-1118
-
-
Muldoon, L.L.1
Neuwelt, E.A.2
Pagel, M.A.3
Weiss, D.L.4
-
59
-
-
0030225915
-
Mucolipidosis type II in a domestic shorthair cat
-
Hubler M, Haskins ME, Arnold S, Kaser-Hotz B, Bosshard NU, et al. 1996. Mucolipidosis type II in a domestic shorthair cat. J. Small Anim. Pract. 37:435-41
-
(1996)
J. Small Anim. Pract.
, vol.37
, pp. 435-441
-
-
Hubler, M.1
Haskins, M.E.2
Arnold, S.3
Kaser-Hotz, B.4
Bosshard, N.U.5
-
60
-
-
34247138344
-
Circadian rhythm of intraocular pressure in cats
-
Del Sole MJ, Sande PH, Bernades JM, Aba MA, Rosenstein RE. 2007. Circadian rhythm of intraocular pressure in cats. Vet. Ophthalmol. 10:155-61
-
(2007)
Vet. Ophthalmol.
, vol.10
, pp. 155-161
-
-
Del Sole, M.J.1
Sande, P.H.2
Bernades, J.M.3
Aba, M.A.4
Rosenstein, R.E.5
-
62
-
-
42549172673
-
Feline primary open angle glaucoma
-
Jacobi S, Dubielzig RR. 2008. Feline primary open angle glaucoma. Vet. Ophthalmol. 11:162-65
-
(2008)
Vet. Ophthalmol.
, vol.11
, pp. 162-165
-
-
Jacobi, S.1
Dubielzig, R.R.2
-
63
-
-
11244345510
-
Feline glaucoma. Clinical and morphological aspects (a retrospective study of 38 cases)
-
Walde I, Rapp E. 1993. Feline glaucoma. Clinical and morphological aspects (a retrospective study of 38 cases). Eur. J. Comp. Anim. Pract. 4:87-105
-
(1993)
Eur. J. Comp. Anim. Pract.
, vol.4
, pp. 87-105
-
-
Walde, I.1
Rapp, E.2
-
66
-
-
0020790679
-
Hereditary progressive retinal atrophy in the Abyssinian cat
-
Narfström K. 1983. Hereditary progressive retinal atrophy in the Abyssinian cat. J. Hered. 74: 273-76
-
(1983)
J. Hered.
, vol.74
, pp. 273-276
-
-
Narfström, K.1
-
67
-
-
70249125068
-
Retinal degeneration in the Abyssinian and Somali cat (rdAc): Correlation between genotype and phenotype and rdAc allele frequency in two continents
-
Narfström K, David V, Jarret O, Beatty J, Barrs V, et al. 2009. Retinal degeneration in the Abyssinian and Somali cat (rdAc): correlation between genotype and phenotype and rdAc allele frequency in two continents. Vet. Ophthalmol. 12:285-91
-
(2009)
Vet. Ophthalmol.
, vol.12
, pp. 285-291
-
-
Narfström, K.1
David, V.2
Jarret, O.3
Beatty, J.4
Barrs, V.5
-
68
-
-
0021997226
-
Progressive retinal atrophy in the Abyssinian cat: Studies of the DC-recorded electroretinogram and the standing potential of the eye
-
Narfström KL, Nilsson SE, Andersson BE. 1985. Progressive retinal atrophy in the Abyssinian cat: studies of the DC-recorded electroretinogram and the standing potential of the eye. Br. J. Ophthalmol. 69:618-23
-
(1985)
Br. J. Ophthalmol.
, vol.69
, pp. 618-623
-
-
Narfström, K.L.1
Nilsson, S.E.2
Andersson, B.E.3
-
69
-
-
0023692917
-
Hereditary retinal degeneration in the Abyssinian cat: Developmental studies using clinical electroretinography
-
Narfström K, Wilen M, Andersson BE. 1988. Hereditary retinal degeneration in the Abyssinian cat: developmental studies using clinical electroretinography. Doc. Ophthalmol. 69:111-18
-
(1988)
Doc. Ophthalmol.
, vol.69
, pp. 111-118
-
-
Narfström, K.1
Wilen, M.2
Andersson, B.E.3
-
70
-
-
1342300778
-
Abnormal dark-adapted ERG in cats heterozygous for a recessively inherited rod-cone degeneration
-
Ekesten B, Narfström K. 2004. Abnormal dark-adapted ERG in cats heterozygous for a recessively inherited rod-cone degeneration. Vet. Ophthalmol. 7:63-67
-
(2004)
Vet. Ophthalmol.
, vol.7
, pp. 63-67
-
-
Ekesten, B.1
Narfström, K.2
-
71
-
-
0032310887
-
Cone positive off-response in normal and dystrophic cats
-
Ekesten B, Narfström K. 1998. Cone positive off-response in normal and dystrophic cats. Doc. Ophthalmol. 97:9-21
-
(1998)
Doc. Ophthalmol.
, vol.97
, pp. 9-21
-
-
Ekesten, B.1
Narfström, K.2
-
73
-
-
0024367065
-
Morphological findings during retinal development and maturation in hereditary rod-cone degeneration in Abyssinian cats
-
Narfström K, Nilsson SE. 1989. Morphological findings during retinal development and maturation in hereditary rod-cone degeneration in Abyssinian cats. Exp. Eye Res. 49:611-28
-
(1989)
Exp. Eye Res.
, vol.49
, pp. 611-628
-
-
Narfström, K.1
Nilsson, S.E.2
-
74
-
-
0035378914
-
Immunohistochemical studies of cone photoreceptors and cells of the inner retina in feline rod-cone degeneration
-
Narfström K, Ehinger B, Bruun A. 2001. Immunohistochemical studies of cone photoreceptors and cells of the inner retina in feline rod-cone degeneration. Vet. Ophthalmol. 4:141-45
-
(2001)
Vet. Ophthalmol.
, vol.4
, pp. 141-145
-
-
Narfström, K.1
Ehinger, B.2
Bruun, A.3
-
75
-
-
0028044118
-
An early decrease in interphotoreceptor retinoid-binding protein gene expression in Abyssinian cats homozygous for hereditary rodcone degeneration
-
Wiggert B, van Veen T, Kutty G, Lee L, Nickerson J, et al. 1994. An early decrease in interphotoreceptor retinoid-binding protein gene expression in Abyssinian cats homozygous for hereditary rodcone degeneration. Cell Tissue Res. 278:291-98
-
(1994)
Cell Tissue Res.
, vol.278
, pp. 291-298
-
-
Wiggert, B.1
Van Veen, T.2
Kutty, G.3
Lee, L.4
Nickerson, J.5
-
76
-
-
0024344070
-
Retinal sensitivity in hereditary retinal degeneration in Abyssinian cats: Electrophysiological similarities between man and cat
-
Narfström K, Arden GB, Nilsson SE. 1989. Retinal sensitivity in hereditary retinal degeneration in Abyssinian cats: electrophysiological similarities between man and cat. Br. J. Ophthalmol. 73: 516-21
-
(1989)
Br. J. Ophthalmol.
, vol.73
, pp. 516-521
-
-
Narfström, K.1
Arden, G.B.2
Nilsson, S.E.3
-
77
-
-
30744473953
-
Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration
-
Hyman JA, Vaegan, Lei B, Narfström KL. 2005. Electrophysiologic differentiation of homozygous and heterozygous Abyssinian-crossbred cats with late-onset hereditary retinal degeneration. Am. J. Vet. Res. 66:1914-21
-
(2005)
Am. J. Vet. Res.
, vol.66
, pp. 1914-1921
-
-
Hyman, J.A.1
Vaegan Lei, B.2
Narfström, K.L.3
-
78
-
-
11344280657
-
Optimal discrimination of an Abyssinian cat recessive retinal degeneration: A short electroretinogram protocol is more efficient than a long one
-
Vaegan, Narfström K. 2004. Optimal discrimination of an Abyssinian cat recessive retinal degeneration: a short electroretinogram protocol is more efficient than a long one. Clin. Exp. Ophthalmol. 32:619-25
-
(2004)
Clin. Exp. Ophthalmol.
, vol.32
, pp. 619-625
-
-
Vaegan, N.K.1
-
79
-
-
33644534515
-
A(max) is the best a-wave measure for classifying Abyssinian cat rod/cone dystrophy
-
Vaegan, Narfström K. 2005. A(max) is the best a-wave measure for classifying Abyssinian cat rod/cone dystrophy. Doc. Ophthalmol. 111:33-38
-
(2005)
Doc. Ophthalmol.
, vol.111
, pp. 33-38
-
-
Vaegan, N.K.1
-
80
-
-
0021357844
-
Human rhodopsin measurement using a T.V.-based imaging fundus reflectometer
-
Faulkner DJ, Kemp CM. 1984. Human rhodopsin measurement using a T.V.-based imaging fundus reflectometer. Vis. Res. 24:221-31
-
(1984)
Vis. Res.
, vol.24
, pp. 221-231
-
-
Faulkner, D.J.1
Kemp, C.M.2
-
81
-
-
0024314189
-
Rhodopsin levels and rod-mediated function in Abyssinian cats with hereditary retinal degeneration
-
Jacobson SEG, Kemp CM, Narfström K, Nilsson SE. 1989. Rhodopsin levels and rod-mediated function in Abyssinian cats with hereditary retinal degeneration. Exp. Eye Res. 49:843-52
-
(1989)
Exp. Eye Res.
, vol.49
, pp. 843-852
-
-
Jacobson, S.E.G.1
Kemp, C.M.2
Narfström, K.3
Nilsson, S.E.4
-
82
-
-
0033709187
-
Continuous monitoring of the stimulated area in multifocal ERG
-
Seeliger MW, Narfström K, Reinhard J, Zrenner E, Sutter E. 2000. Continuous monitoring of the stimulated area in multifocal ERG. Doc. Ophthalmol. 100:167-84
-
(2000)
Doc. Ophthalmol.
, vol.100
, pp. 167-184
-
-
Seeliger, M.W.1
Narfström, K.2
Reinhard, J.3
Zrenner, E.4
Sutter, E.5
-
83
-
-
0034092390
-
Functional assessment of the regional distribution of disease in a cat model of hereditary retinal degeneration
-
Seeliger MW, Narfström K. 2000. Functional assessment of the regional distribution of disease in a cat model of hereditary retinal degeneration. Investig. Ophthalmol. Vis. Sci. 41:1998-2005
-
(2000)
Investig. Ophthalmol. Vis. Sci.
, vol.41
, pp. 1998-2005
-
-
Seeliger, M.W.1
Narfström, K.2
-
84
-
-
0029743273
-
Nitric oxide as a mediator of parasympathetic vasodilation in ocular and extraocular tissues in the rabbit
-
Nilsson SF. 1996. Nitric oxide as a mediator of parasympathetic vasodilation in ocular and extraocular tissues in the rabbit. Investig. Ophthalmol. Vis. Sci. 37:2110-19
-
(1996)
Investig. Ophthalmol. Vis. Sci.
, vol.37
, pp. 2110-2119
-
-
Nilsson, S.F.1
-
85
-
-
0035065992
-
Ocular blood flow and retinal metabolism in Abyssinian cats with hereditary retinal degeneration
-
Nilsson SF, Maepea O, Alm A, Narfström K. 2001. Ocular blood flow and retinal metabolism in Abyssinian cats with hereditary retinal degeneration. Investig. Ophthalmol. Vis. Sci. 42:1038-44
-
(2001)
Investig. Ophthalmol. Vis. Sci.
, vol.42
, pp. 1038-1044
-
-
Nilsson, S.F.1
Maepea, O.2
Alm, A.3
Narfström, K.4
-
86
-
-
28444478006
-
In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy
-
Seeliger MW, Beck SC, Pereyra-Muñoz N, Dangel S, Tsai JY, et al. 2005. In vivo confocal imaging of the retina in animal models using scanning laser ophthalmoscopy. Vis. Res. 45:3512-19
-
(2005)
Vis. Res.
, vol.45
, pp. 3512-3519
-
-
Seeliger, M.W.1
Beck, S.C.2
Pereyra-Muñoz, N.3
Dangel, S.4
Tsai, J.Y.5
-
87
-
-
33748109425
-
The electroretinogram components in Abyssinian cats with hereditary retinal degeneration
-
Kang Derwent JJ, Padnick-Silver L, McRipley M, Guiliano E, Linsenmeier RA, Narfström K. 2006. The electroretinogram components in Abyssinian cats with hereditary retinal degeneration. Investig. Ophthalmol. Vis. Sci. 47:3673-82
-
(2006)
Investig. Ophthalmol. Vis. Sci.
, vol.47
, pp. 3673-3682
-
-
Kang Derwent, J.J.1
Padnick-Silver, L.2
McRipley, M.3
Guiliano, E.4
Linsenmeier, R.A.5
Narfström, K.6
-
88
-
-
33748097857
-
Retinal oxygenation and oxygen metabolism in Abyssinian cats with a hereditary retinal degeneration
-
Padnick-Silver L, Kang Derwent JJ, Guiliano E, Narfström K, Linsenmeier RA. 2006. Retinal oxygenation and oxygen metabolism in Abyssinian cats with a hereditary retinal degeneration. Investig. Ophthalmol. Vis. Sci. 47:3683-89
-
(2006)
Investig. Ophthalmol. Vis. Sci.
, vol.47
, pp. 3683-3689
-
-
Padnick-Silver, L.1
Kang Derwent, J.J.2
Guiliano, E.3
Narfström, K.4
Linsenmeier, R.A.5
-
89
-
-
0037227766
-
The vertebrate primary cilium is a sensory organelle
-
Pazour GJ, Witman GB. 2003. The vertebrate primary cilium is a sensory organelle. Curr. Opin. Cell Biol. 15:105-10
-
(2003)
Curr. Opin. Cell Biol.
, vol.15
, pp. 105-110
-
-
Pazour, G.J.1
Witman, G.B.2
-
90
-
-
77958185645
-
Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds
-
Menotti-Raymond M, David VA, Pflueger S, Roelke ME, Kehler J, et al. 2010. Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds. Vet. J. 186:32-38
-
(2010)
Vet. J.
, vol.186
, pp. 32-38
-
-
Menotti-Raymond, M.1
David, V.A.2
Pflueger, S.3
Roelke, M.E.4
Kehler, J.5
-
91
-
-
33748664605
-
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.Am
-
den Hollander AI, Koenekoop RK, Yzer S, Lopez I, Arends ML, et al. 2006. Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.Am. J. Hum.Genet. 79: 556-61
-
(2006)
J. Hum.Genet.
, vol.79
, pp. 556-561
-
-
Den Hollander, A.I.1
Koenekoop, R.K.2
Yzer, S.3
Lopez, I.4
Arends, M.L.5
-
92
-
-
33846076617
-
The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome
-
Baala L, Romano S, Khaddour R, Saunier S, Smith UM, et al. 2007. The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome. Am. J. Hum. Genet. 80:186-94
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 186-194
-
-
Baala, L.1
Romano, S.2
Khaddour, R.3
Saunier, S.4
Smith, U.M.5
-
93
-
-
33745230448
-
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
-
Sayer JA, Otto EA, O'Toole JF, Nurnberg G, Kennedy MA, et al. 2006. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nat. Genet. 38: 674-81
-
(2006)
Nat. Genet.
, vol.38
, pp. 674-681
-
-
Sayer, J.A.1
Otto, E.A.2
O'Toole, J.F.3
Nurnberg, G.4
Kennedy, M.A.5
-
94
-
-
34347225615
-
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders
-
Brancati F, Barrano G, Silhavy JL, Marsh SE, Travaglini L. et al. 2007. CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. Am. J. Hum. Genet. 81: 104-13
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 104-113
-
-
Brancati, F.1
Barrano, G.2
Silhavy, J.L.3
Marsh, S.E.4
Travaglini, L.5
-
95
-
-
33745225873
-
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome
-
Valente EM, Silhavy JL, Brancati F, Barrano G, Krishnaswami SR, et al. 2006. Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. Nat. Genet. 38: 623-25
-
(2006)
Nat. Genet.
, vol.38
, pp. 623-625
-
-
Valente, E.M.1
Silhavy, J.L.2
Brancati, F.3
Barrano, G.4
Krishnaswami, S.R.5
-
96
-
-
41349103272
-
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome
-
Leitch CC, Zaghloul NA, Davis EE, Stoetzel C, Diaz-Font A, et al. 2008. Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nat. Genet. 40:443-48
-
(2008)
Nat. Genet.
, vol.40
, pp. 443-448
-
-
Leitch, C.C.1
Zaghloul, N.A.2
Davis, E.E.3
Stoetzel, C.4
Diaz-Font, A.5
-
97
-
-
0021960701
-
Autosomal dominant progressive retinal atrophy in Abyssinian cats
-
Barnett KC, Curtis R. 1985. Autosomal dominant progressive retinal atrophy in Abyssinian cats. J. Hered. 76:168-70
-
(1985)
J. Hered.
, vol.76
, pp. 168-170
-
-
Barnett, K.C.1
Curtis, R.2
-
98
-
-
0026076564
-
Autosomal dominant rod-cone dysplasia in the Rdy cat. 2. Electrophysiological findings
-
Leon A, Hussain AA, Curtis R. 1991. Autosomal dominant rod-cone dysplasia in the Rdy cat. 2. Electrophysiological findings. Exp. Eye Res. 53:489-502
-
(1991)
Exp. Eye Res.
, vol.53
, pp. 489-502
-
-
Leon, A.1
Hussain, A.A.2
Curtis, R.3
-
99
-
-
0025079681
-
Autosomal dominant rod-cone dysplasia in the Rdy cat. 1. Light and electron microscopic findings
-
Leon A, Curtis R. 1990. Autosomal dominant rod-cone dysplasia in the Rdy cat. 1. Light and electron microscopic findings. Exp. Eye Res. 51:361-81
-
(1990)
Exp. Eye Res.
, vol.51
, pp. 361-381
-
-
Leon, A.1
Curtis, R.2
-
100
-
-
39449091111
-
The Cis-regulatory logic of the mammalian photoreceptor transcriptional network
-
Hsiau TH-C, Diaconu C, Myers CA, Lee J, Cepko CL, Corbo JC. 2007. The Cis-regulatory logic of the mammalian photoreceptor transcriptional network. PLoS ONE 7:e643
-
(2007)
PLoS ONE
, vol.7
-
-
Th-C, H.1
Diaconu, C.2
Myers, C.A.3
Lee, J.4
Cepko, C.L.5
Corbo, J.C.6
-
101
-
-
0030781996
-
Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes
-
Chen S, Wang QL, Nie Z, Sun H, Lennon G, et al. 1997. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron 19:1017-30
-
(1997)
Neuron
, vol.19
, pp. 1017-1030
-
-
Chen, S.1
Wang, Q.L.2
Nie, Z.3
Sun, H.4
Lennon, G.5
-
102
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor
-
Freund CL, Gregory-Evans CY, Furukawa T, Papaioannou M, Looser J, et al. 1997. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor. Cell 91:543-53
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregory-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
-
103
-
-
0037091102
-
Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy
-
Chen S, Wang QL, Xu S, Liu I, Li LY, et al. 2002. Functional analysis of cone-rod homeobox (CRX) mutations associated with retinal dystrophy. Hum. Mol. Genet. 11:873-84
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 873-884
-
-
Chen, S.1
Wang, Q.L.2
Xu, S.3
Liu, I.4
Li, L.Y.5
-
104
-
-
85081821459
-
Analysis of the CRX protein profile in the Rdy cat model suggests molecular mechanism of pathology
-
Baltimore, MD
-
Deckman KH, Khalsa A, Lin J, David VA, Menotti-Raymond M, Narfström K. 2010. Analysis of the CRX protein profile in the Rdy cat model suggests molecular mechanism of pathology. In 5th Int. Conf.: Adv. Canine Feline Genomics Inherit. Dis., Baltimore, MD
-
(2010)
5th Int. Conf.: Adv. Canine Feline Genomics Inherit. Dis.
-
-
Deckman, K.H.1
Khalsa, A.2
Lin, J.3
David, V.A.4
Menotti-Raymond, M.5
Narfström, K.6
-
105
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. 1997. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell 91:531-41
-
(1997)
Cell
, vol.91
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
106
-
-
4344665205
-
Photoreceptor-specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors
-
ChengH,KhannaH,OhEC,HicksD,MittonKP, SwaroopA.2004. Photoreceptor- specific nuclear receptor NR2E3 functions as a transcriptional activator in rod photoreceptors. Hum. Mol. Genet. 13:1563-75
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1563-1575
-
-
Cheng, H.1
Khanna, H.2
Oh, E.C.3
Hicks, D.4
Mitton, K.P.5
Swaroop, A.6
-
107
-
-
85081819500
-
Analysis of the CRX protein profile in the Rdy cat model suggests molecular mechanism of pathology
-
Washington DC
-
Deckman KH, Dempster K, Khalsa A, Lin J, David VA, et al. 2011. Analysis of the CRX protein profile in the Rdy cat model suggests molecular mechanism of pathology. Presented at Am. Soc. Biochem. Mol. Biol. Exp. Biol. Conf., Washington, DC
-
(2011)
Am. Soc. Biochem. Mol. Biol. Exp. Biol. Conf.
-
-
Deckman, K.H.1
Dempster, K.2
Khalsa, A.3
Lin, J.4
David, V.A.5
-
108
-
-
80054741160
-
RNAi: A potential new class of therapeutic for human genetic disease
-
Seyhan AA. 2011. RNAi: a potential new class of therapeutic for human genetic disease. Hum. Genet. 130:583-605
-
(2011)
Hum. Genet.
, vol.130
, pp. 583-605
-
-
Seyhan, A.A.1
-
109
-
-
33645145491
-
Large animal models and gene therapy
-
Casal M, Haskins M. 2006. Large animal models and gene therapy. Eur. J. Hum. Genet. 14:266-72
-
(2006)
Eur. J. Hum. Genet.
, vol.14
, pp. 266-272
-
-
Casal, M.1
Haskins, M.2
-
110
-
-
46249091156
-
Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)
-
Tam LC, Kiang AS, Kennan A, Kenna PF, Chadderton N, et al. 2008. Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10). Hum. Mol. Genet. 17:2084-100
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2084-2100
-
-
Tam, L.C.1
Kiang, A.S.2
Kennan, A.3
Kenna, P.F.4
Chadderton, N.5
-
111
-
-
63949087144
-
Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy
-
Chadderton N, Millington-Ward S, Palfi A,O'Reilly M, Tuohy G, et al. 2009. Improved retinal function in a mouse model of dominant retinitis pigmentosa following AAV-delivered gene therapy. Mol. Ther. 17:593-99
-
(2009)
Mol. Ther.
, vol.17
, pp. 593-599
-
-
Chadderton, N.1
Millington-Ward, S.2
Palfi, A.3
O'Reilly, M.4
Tuohy, G.5
-
112
-
-
79953314650
-
Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosa
-
Millington-Ward S, Chadderton N, O'Reilly M, Palfi A, Goldmann T, et al. 2011. Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosa. Mol. Ther. 19:642-49
-
(2011)
Mol. Ther.
, vol.19
, pp. 642-649
-
-
Millington-Ward, S.1
Chadderton, N.2
O'Reilly, M.3
Palfi, A.4
Goldmann, T.5
-
113
-
-
77949733904
-
Adeno-associated virus-mediated rhodopsin replacement provides therapeutic benefit in mice with a targeted disruption of the rhodopsin gene
-
Palfi A, Millington-Ward S, Chadderton N, O'Reilly M, Goldmann T, et al. 2010. Adeno-associated virus-mediated rhodopsin replacement provides therapeutic benefit in mice with a targeted disruption of the rhodopsin gene. Hum. Gene Ther. 21:311-23
-
(2010)
Hum. Gene Ther.
, vol.21
, pp. 311-323
-
-
Palfi, A.1
Millington-Ward, S.2
Chadderton, N.3
O'Reilly, M.4
Goldmann, T.5
-
114
-
-
84855931333
-
Suppression of rds expression by siRNA and gene replacement strategies for gene therapy using rAAV vector
-
Petrs-SilvaH, Yasumura D, Matthes MT, LaVailMM,Lewin AS, HauswirthWW. 2012. Suppression of rds expression by siRNA and gene replacement strategies for gene therapy using rAAV vector. Adv. Exp. Med. Biol. 723:215-23
-
(2012)
Adv. Exp. Med. Biol.
, vol.723
, pp. 215-223
-
-
Petrs-Silva, H.1
Yasumura, D.2
Matthes, M.T.3
Lavail, M.M.4
Lewin, A.S.5
Hauswirth, W.W.6
-
115
-
-
79959635350
-
Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation
-
Vasireddy V, Chavali VR, Joseph VT, Kadam R, Lin JH, et al. 2011. Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation. PLoS ONE 6:e21193
-
(2011)
PLoS ONE
, vol.6
-
-
Vasireddy, V.1
Chavali, V.R.2
Joseph, V.T.3
Kadam, R.4
Lin, J.H.5
-
116
-
-
58149484922
-
Ocular gene therapy: Current progress and future prospects
-
Colella P, Cotugno G, Auricchio A. 2009. Ocular gene therapy: current progress and future prospects. Trends Mol. Med. 15:23-31
-
(2009)
Trends Mol. Med.
, vol.15
, pp. 23-31
-
-
Colella, P.1
Cotugno, G.2
Auricchio, A.3
-
117
-
-
0035032662
-
Gene therapy restores vision in a canine model of childhood blindness
-
Acland GM, Aguirre GD, Ray J, Zhang Q, Aleman TS, et al. 2001. Gene therapy restores vision in a canine model of childhood blindness. Nat. Genet. 28:92-95
-
(2001)
Nat. Genet.
, vol.28
, pp. 92-95
-
-
Acland, G.M.1
Aguirre, G.D.2
Ray, J.3
Zhang, Q.4
Aleman, T.S.5
-
118
-
-
33644525947
-
Assessment of structure and function over a 3-year period after gene transfer in RPE65/dogs
-
Narfström K, Vaegan, Katz M, Bragadottir R, Rakoczy EP, Seeliger M. 2005. Assessment of structure and function over a 3-year period after gene transfer in RPE65/dogs. Doc. Ophthalmol. 111:39-48
-
(2005)
Doc. Ophthalmol.
, vol.111
, pp. 39-48
-
-
Narfström, K.1
Vaegan Katz, M.2
Bragadottir, R.3
Rakoczy, E.P.4
Seeliger, M.5
-
119
-
-
84855978522
-
Gene delivery of wild-type rhodopsin rescues retinal function in an autosomal dominant retinitis pigmentosa mouse model
-
Mao H, Gorbatyuk MS, Hauswirth WW, Lewin AS. 2012. Gene delivery of wild-type rhodopsin rescues retinal function in an autosomal dominant retinitis pigmentosa mouse model. Adv. Exp.Med. Biol. 723:199-205
-
(2012)
Adv. Exp.Med. Biol.
, vol.723
, pp. 199-205
-
-
Mao, H.1
Gorbatyuk, M.S.2
Hauswirth, W.W.3
Lewin, A.S.4
-
121
-
-
84861819775
-
A review and update on the current status of stem cell therapy and the retina
-
Ong JM, da Cruz L. 2012. A review and update on the current status of stem cell therapy and the retina. Br. Med. Bull. 102:133-46
-
(2012)
Br. Med. Bull.
, vol.102
, pp. 133-146
-
-
Ong, J.M.1
Da Cruz, L.2
-
122
-
-
74049111551
-
Induced pluripotent stem cell therapies for retinal disease
-
Comyn O, Lee E, MacLaren RE. 2010. Induced pluripotent stem cell therapies for retinal disease. Curr. Opin. Neurol. 23:4-9
-
(2010)
Curr. Opin. Neurol.
, vol.23
, pp. 4-9
-
-
Comyn, O.1
Lee, E.2
MacLaren, R.E.3
-
123
-
-
66749139607
-
Stepwise differentiation of pluripotent stem cells into retinal cells
-
Osakada F, Ikeda H, Sasai Y, TakahashiM. 2009. Stepwise differentiation of pluripotent stem cells into retinal cells. Nat. Protoc. 4:811-24
-
(2009)
Nat. Protoc.
, vol.4
, pp. 811-824
-
-
Osakada, F.1
Ikeda, H.2
Sasai, Y.3
Takahashi, M.4
-
124
-
-
65549115150
-
Generation of retinal cells from mouse and human induced pluripotent stem cells
-
Hirami Y, Osakada F, Takahashi K, Okita K, Yamanaka S, et al. 2009. Generation of retinal cells from mouse and human induced pluripotent stem cells. Neurosci. Lett. 458:126-31
-
(2009)
Neurosci. Lett.
, vol.458
, pp. 126-131
-
-
Hirami, Y.1
Osakada, F.2
Takahashi, K.3
Okita, K.4
Yamanaka, S.5
-
125
-
-
84857643783
-
Embryonic stem cell trials for macular degeneration: A preliminary report
-
Schwartz SD, Hubschman JP, Heilwell G, Franco-Cardenas V, Pan CK, et al. 2012. Embryonic stem cell trials for macular degeneration: a preliminary report. Lancet 379:713-20
-
(2012)
Lancet
, vol.379
, pp. 713-720
-
-
Schwartz, S.D.1
Hubschman, J.P.2
Heilwell, G.3
Franco-Cardenas, V.4
Pan, C.K.5
-
126
-
-
34250177644
-
Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic cat
-
Klassen H, Schwartz PH, Ziaeian B, Nethercott H, Young MJ, et al. 2007. Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic cat. Vet. Ophthalmol. 10:245-53
-
(2007)
Vet. Ophthalmol.
, vol.10
, pp. 245-253
-
-
Klassen, H.1
Schwartz, P.H.2
Ziaeian, B.3
Nethercott, H.4
Young, M.J.5
-
127
-
-
65349156908
-
Functional and structural assessment of retinal sheet allograft transplantation in feline hereditary retinal degeneration
-
Seiler MJ, Aramant RB, Seeliger MW, Bragadottir R, Mahoney M, Narfström K. 2009. Functional and structural assessment of retinal sheet allograft transplantation in feline hereditary retinal degeneration. Vet. Ophthalmol. 12:158-69
-
(2009)
Vet. Ophthalmol.
, vol.12
, pp. 158-169
-
-
Seiler, M.J.1
Aramant, R.B.2
Seeliger, M.W.3
Bragadottir, R.4
Mahoney, M.5
Narfström, K.6
-
128
-
-
0034711293
-
Functional domains of the cone-rod homeobox (CRX) transcription factor
-
Chau KY, Chen S, Zack DJ, Ono SJ. 2000. Functional domains of the cone-rod homeobox (CRX) transcription factor. J. Biol. Chem. 275:37264-70
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 37264-37270
-
-
Chau, K.Y.1
Chen, S.2
Zack, D.J.3
Ono, S.J.4
|