Noriyuki Azuma

Summary

Affiliation: National Center for Child Health and Development
Country: Japan

Publications

  1. ncbi request reprint Three novel mutations of the PAX6 gene in Japanese aniridia patients
    Toshio Kawano
    Department of Ophthalmology, Hamamatsu University School of Medicine, Hamamatsu, Japan
    J Hum Genet 52:571-4. 2007
  2. ncbi request reprint The Pax6 isoform bearing an alternative spliced exon promotes the development of the neural retinal structure
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Developent, Tokyo, Japan
    Hum Mol Genet 14:735-45. 2005
  3. pmc Mutations of the PAX6 gene detected in patients with a variety of optic-nerve malformations
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Hum Genet 72:1565-70. 2003
  4. ncbi request reprint Early vitreous surgery for aggressive posterior retinopathy of prematurity
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 142:636-43. 2006
  5. ncbi request reprint Transdifferentiation of the retinal pigment epithelia to the neural retina by transfer of the Pax6 transcriptional factor
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo 157 8535, Japan
    Hum Mol Genet 14:1059-68. 2005
  6. doi request reprint Clinical features of congenital retinal folds
    Sachiko Nishina
    Division of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 153:81-7.e1. 2012
  7. doi request reprint Effect of early vitreous surgery for aggressive posterior retinopathy of prematurity detected by fundus fluorescein angiography
    Sachiko Nishina
    The Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Ophthalmology 116:2442-7. 2009
  8. doi request reprint Evaluation of scleral buckling for stage 4A retinopathy of prematurity by fluorescein angiography
    Tae Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 148:544-550.e1. 2009
  9. doi request reprint Risk factors for recurrent fibrovascular proliferation in aggressive posterior retinopathy of prematurity after early vitreous surgery
    Tadashi Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 150:10-15.e1. 2010
  10. doi request reprint Visual outcomes after early vitreous surgery for aggressive posterior retinopathy of prematurity
    Noriyuki Azuma
    Department of Ophthalmology and Laboratory of Cell Biology, National Center for Child Health and Development, Tokyo, Japan
    JAMA Ophthalmol 131:1309-13. 2013

Detail Information

Publications55

  1. ncbi request reprint Three novel mutations of the PAX6 gene in Japanese aniridia patients
    Toshio Kawano
    Department of Ophthalmology, Hamamatsu University School of Medicine, Hamamatsu, Japan
    J Hum Genet 52:571-4. 2007
    ..The database for PAX6 gene mutation has been made using a graphical data display system MutationView ( http://mutview.dmb.med.keio.ac.jp/ )...
  2. ncbi request reprint The Pax6 isoform bearing an alternative spliced exon promotes the development of the neural retinal structure
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Developent, Tokyo, Japan
    Hum Mol Genet 14:735-45. 2005
    ..We propose that Pax6(+5a) induces a developmental cascade in the prospective fovea, area centralis or visual streak region that leads to the formation of a retinal architecture bearing densely packed visual cells...
  3. pmc Mutations of the PAX6 gene detected in patients with a variety of optic-nerve malformations
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Hum Genet 72:1565-70. 2003
    ..Because PAX2 gene mutations were detected in papillorenal syndrome, alternation of PAX2 function by PAX6 mutations may affect phenotypic manifestations of optic-nerve malformations...
  4. ncbi request reprint Early vitreous surgery for aggressive posterior retinopathy of prematurity
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 142:636-43. 2006
    ..To assess the efficacy of early vitrectomy for aggressive posterior retinopathy of prematurity (ROP) to stop progression of retinal detachment...
  5. ncbi request reprint Transdifferentiation of the retinal pigment epithelia to the neural retina by transfer of the Pax6 transcriptional factor
    Noriyuki Azuma
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo 157 8535, Japan
    Hum Mol Genet 14:1059-68. 2005
    ..Our results provide an evidence of retinogenic potential of nearly mature RPE and a cue for new therapeutic approaches to regenerate functional NR in patients with a visual loss...
  6. doi request reprint Clinical features of congenital retinal folds
    Sachiko Nishina
    Division of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 153:81-7.e1. 2012
    ..To investigate the clinical features and prognosis of congenital retinal folds without systemic associations...
  7. doi request reprint Effect of early vitreous surgery for aggressive posterior retinopathy of prematurity detected by fundus fluorescein angiography
    Sachiko Nishina
    The Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Ophthalmology 116:2442-7. 2009
    ..To assess the effect of early vitrectomy for aggressive posterior retinopathy of prematurity (APROP) using fundus fluorescein angiography...
  8. doi request reprint Evaluation of scleral buckling for stage 4A retinopathy of prematurity by fluorescein angiography
    Tae Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 148:544-550.e1. 2009
    ..To determine the early efficacy of scleral buckling for active neovascularization by fundus fluorescein angiography (FA) in eyes with stage 4A retinopathy of prematurity...
  9. doi request reprint Risk factors for recurrent fibrovascular proliferation in aggressive posterior retinopathy of prematurity after early vitreous surgery
    Tadashi Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 150:10-15.e1. 2010
    ..To analyze risk factors for postoperative recurrence of fibrovascular tissue in eyes with aggressive posterior retinopathy of prematurity (AP ROP) treated with early vitreous surgery...
  10. doi request reprint Visual outcomes after early vitreous surgery for aggressive posterior retinopathy of prematurity
    Noriyuki Azuma
    Department of Ophthalmology and Laboratory of Cell Biology, National Center for Child Health and Development, Tokyo, Japan
    JAMA Ophthalmol 131:1309-13. 2013
    ..Early vitreous surgery might achieve prompt regression of neovascular activity and a high incidence of retinal reattachment...
  11. doi request reprint A case of aniridia with unilateral Peters anomaly
    Mayu Sawada
    Department of Ophthalmology, Hamamatsu University School of Medicine, Hamamatsu, Japan
    J AAPOS 15:104-6. 2011
    ..We report a child with aniridia and Peters anomaly associated with a PAX6 gene mutation...
  12. doi request reprint Exudative retinal detachment following cataract surgery in Hallermann-Streiff syndrome
    Sachiko Nishina
    Department of Ophthalmology, National Center for Child Health and Development, 2 10 1 Ohkura, Setagaya Ku, Tokyo 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol 246:453-5. 2008
    ..To report two cases of Hallermann-Streiff syndrome with exudative retinal detachment after cataract surgery...
  13. doi request reprint Surgical outcomes of congenital and developmental cataracts in Japan
    Toshiyuki Nagamoto
    Department of Ophthalmology, Kyorin University School of Medicine, Tokyo, Japan
    Jpn J Ophthalmol 60:127-34. 2016
    ..To retrospectively analyze the surgical outcomes of congenital/developmental cataracts in Japan...
  14. doi request reprint A survey of the surgical treatment of congenital and developmental cataracts in Japan
    Toshiyuki Nagamoto
    Department of Ophthalmology, Kyorin University School of Medicine, Tokyo, Japan
    Jpn J Ophthalmol 59:203-8. 2015
    ..To understand the current practice pattern for the surgical treatment of congenital/developmental cataracts in Japan...
  15. pmc Derivation of human differential photoreceptor cells from adult human dermal fibroblasts by defined combinations of CRX, RAX, OTX2 and NEUROD
    Yuko Seko
    Visual Functions Section, Department of Rehabilitation for Sensory Functions, Research Institute, National Rehabilitation Center for Persons with Disabilities, Tokorozawa, Saitama, 359 8555, Japan Department of Reproductive Biology, Center for Regenerative Medicine, National Institute for Child Health and Development, Okura, Setagaya, Tokyo, 157 8535, Japan
    Genes Cells 19:198-208. 2014
    ..Both the NRL gene and the NR2E3 gene were endogenously up-regulated in induced photoreceptor cells, implying that exogenous CRX, RAX, OTX2 and NEUROD, but not NRL, are sufficient to generate rod photoreceptor cells. ..
  16. doi request reprint Clinical features of anterior segment dysgenesis associated with congenital corneal opacities
    Chika Shigeyasu
    Division for Vision Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Megurao ku, Tokyo, Japan
    Cornea 31:293-8. 2012
    ..Anterior segment dysgenesis is one of the main causes of congenital corneal opacities. In this study, we investigated the clinical features and visual outcomes of patients with anterior segment dysgenesis in a large number of cases...
  17. doi request reprint Congenital rotated macula with good vision and binocular function
    Yumi Suzuki
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Jpn J Ophthalmol 53:452-4. 2009
    ..Two patients presented with congenital rotated macula with good vision and binocular function...
  18. pmc Genotype-phenotype correlation of PAX6 gene mutations in aniridia
    Tadashi Yokoi
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, Tokyo, Japan
    Hum Genome Var 3:15052. 2016
    ....
  19. doi request reprint Three cases of rhegmatogenous retinal detachment associated with regressed retinoblastoma after conservative tumor therapy
    Michiko Tanaka
    Departments of Ophthalmology and Laboratory of Cell Biology, and Pathology, National Center for Child Health and Development, Tokyo, Japan
    Retin Cases Brief Rep 8:223-6. 2014
    ..To report three cases of rhegmatogenous retinal detachment associated with regressed retinoblastoma after conservative therapy...
  20. doi request reprint Vascular abnormalities in aggressive posterior retinopathy of prematurity detected by fluorescein angiography
    Tadashi Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Ophthalmology 116:1377-82. 2009
    ..To evaluate fluorescein angiography (FA) in eyes with aggressive posterior retinopathy of prematurity (AP-ROP)...
  21. pmc Establishment of functioning human corneal endothelial cell line with high growth potential
    Tadashi Yokoi
    Department of Ophthalomology, National Center for Child Health and Development, Tokyo, Japan
    PLoS ONE 7:e29677. 2012
    ..This study shows that HCEC cell cycle activation can be achieved by inhibiting CKIs even while maintaining critical pump function and morphology...
  22. ncbi request reprint Pax6-5a promotes neuronal differentiation of murine embryonic stem cells
    Nao Shimizu
    Department of Developmental and Regenerative Biology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan
    Biol Pharm Bull 32:999-1003. 2009
    ..Our Pax6 isoform-expressing ES cell lines may serve as useful models for identifying Pax6-regulated genes that are important for neurogenesis and/or eye development...
  23. pmc Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population
    Katsuhiro Hosono
    Department of Ophthalmology, Hamamatsu University School of Medicine, Hamamatsu, Japan
    PLoS ONE 7:e31036. 2012
    ..Screening for c.4957_4958insA and c.8868C>A mutations in the EYS gene may therefore be very effective for the genetic testing and counseling of RP patients in Japan...
  24. doi request reprint Ocular manifestations and prognosis of shaken baby syndrome in two Japanese children's hospitals
    Yuri Kobayashi
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Jpn J Ophthalmol 53:384-8. 2009
    ..To distinguish the profiles of patients and ophthalmologic features and to describe the prognosis of shaken baby syndrome (SBS) in Japan...
  25. doi request reprint Generation of Retinal Ganglion Cells With Functional Axons From Mouse Embryonic Stem Cells and Induced Pluripotent Stem Cells
    Taku Tanaka
    Department of Ophthalmology and Laboratory for Visual Science National Center for Child Health and Development, Tokyo, Japan
    Invest Ophthalmol Vis Sci 57:3348-59. 2016
    ..We investigated whether self-induced RGCs from mouse embryonic stem cells (mESCs) and induced pluripotent stem cells (miPSCs) are realized by the similar induction protocol...
  26. doi request reprint Electroretinography combined with spectral domain optical coherence tomography to detect retinal damage in shaken baby syndrome
    Yuri Nakayama
    National Center for Child s Health and Development, Tokyo, Japan
    J AAPOS 17:411-3. 2013
    ..Combining spectral domain coherence tomography with focal macular electroretinograms might better estimate the functional damage to the macula in patients with shaken baby syndrome. ..
  27. pmc Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity
    Miki Hiraoka
    Department of Ophthalmology, Nippon Medical School, Tokyo, Japan
    Mol Vis 16:2572-7. 2010
    ..Three genes involving the wingless/int1 (Wnt) receptor signaling pathway-FZD4 for frizzled 4, LRP5 for low-density lipoprotein receptor-related protein 5, and ND for Norrie disease protein-are associated with the development of FEVR...
  28. pmc Electroretinographic effects of retinal dragging and retinal folds in eyes with familial exudative vitreoretinopathy
    Yukari Yaguchi
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, Tokyo, Japan
    Sci Rep 6:30523. 2016
    ..In addition, the function of the retinal ganglion cells appears to be more severely affected compared with the others. ..
  29. ncbi request reprint Successful scleral buckling of late-onset visual decrease in eye with retinal folds
    Yuri Nakayama
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, 2 10 1 Okura Setagaya ku, Tokyo, Japan
    Doc Ophthalmol 133:145-149. 2016
    ..To describe the outcome of scleral buckling to treat radial retinal folds (RFs) that caused a late-onset and sudden visual decrease with impairment of the fovea...
  30. doi request reprint Surgical outcomes of progressive tractional retinal detachment associated with familial exudative vitreoretinopathy
    Takahiro Yamane
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 158:1049-55. 2014
    ..To evaluate various surgeries for treating retinal detachment (RD) associated with familial exudative vitreoretinopathy (FEVR)...
  31. doi request reprint Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype
    Sumito Dateki
    Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, 2 10 1 Ohkura, Setagaya, Tokyo 157 8535, Japan
    J Clin Endocrinol Metab 95:756-64. 2010
    ....
  32. ncbi request reprint Infantile case of occlusive microvascular retinopathy after bone marrow transplantation
    Eriko Kawase
    Department of Ophthalmology, National Center for Child Health and Development, 2 10 1 Okura, Setagaya Ku, Tokyo 157 8535, Japan
    Jpn J Ophthalmol 49:318-20. 2005
    ..A variety of anterior and posterior segment ocular complications following bone marrow transplantation (BMT) have been well documented in adults and children, but retinal complications after BMT in infants have rarely been reported...
  33. ncbi request reprint Two patients with different features of congenital optic disc anomalies in the two eyes
    Yumi Suzuki
    Department of Ophthalmology, National Center for Child Health and Development, 2 10 1, Okura, Setagaya Ku, Tokyo, 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol 244:259-61. 2006
    ..Description of two patients, each with different features of congenital optic disc anomalies in the two eyes...
  34. ncbi request reprint Outer retinal deformity detected by optical coherence tomography in eyes with foveal hypoplasia
    Satoshi Katagiri
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, 2 10 1, Okura, Setagaya Ku, Tokyo, 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol 254:2197-2201. 2016
    ..To investigate the relationship between vision and foveal maturity, especially in foveal hypoplasia exhibiting severe structural immaturity...
  35. doi request reprint Abnormal traction of the vitreous detected by swept-source optical coherence tomography is related to the maculopathy associated with optic disc pits
    Tadashi Yokoi
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, 2 10 1, Okura, Setagaya Ku, Tokyo, 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol 254:675-82. 2016
    ..However, it has long been unclear how the disease begins to develop at these ages. We evaluated the relationship between vitreous structure and maculopathy associated with ODP...
  36. doi request reprint Survey of microphthalmia in Japan
    Sachiko Nishina
    Division of Ophthalmology, National Center for Child Health and Development, 2 10 1 Okura, Tokyo, 157 8535, Japan
    Jpn J Ophthalmol 56:198-202. 2012
    ..To report the current status of patients with microphthalmia based on a cross-sectional survey of patient hospital visits...
  37. ncbi request reprint Scleral window surgery and topical mitomycin C for nanophthalmic uveal effusion complicated by renal failure: case report
    Yumi Suzuki
    Department of Ophthalmology, National Center for Child Health and Development, 2 10 1, Okura, Setagaya Ku, Tokyo, 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol 245:755-7. 2007
    ..To describe the case of a 16-year-old patient with nanophthalmic uveal effusion associated with renal failure that was treated with scleral window surgery and topical administration of mitomycin C (MMC)...
  38. doi request reprint Analysis of the vitreous membrane in a case of type 1 Stickler syndrome
    Tadashi Yokoi
    Department of Ophthalmology, National Center for Child Health and Development, Syowa University East Hospital, Tokyo, Japan
    Graefes Arch Clin Exp Ophthalmol 247:715-8. 2009
    ..Although retinal detachment is characteristic of this syndrome, the pathogenesis is unknown...
  39. ncbi request reprint Outcome of early surgery for bilateral congenital cataracts in eyes with microcornea
    Sachiko Nishina
    Department of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Ophthalmol 144:276-280. 2007
    ..To report the outcome of early surgery for bilateral congenital cataracts in eyes with microcornea...
  40. ncbi request reprint Different foveal schisis patterns in each retinal layer in eyes with hereditary juvenile retinoschisis evaluated by en-face optical coherence tomography
    Tomoyo Yoshida-Uemura
    Department of Ophthalmology and Laboratory for Visual Science, National Center for Child Health and Development, 2 10 1 Okura Setagaya ku, Tokyo, 157 8535, Japan
    Graefes Arch Clin Exp Ophthalmol . 2016
    ..To analyze the structures of schisis in eyes with hereditary juvenile retinoschisis using en-face optical coherence tomography (OCT) imaging...
  41. doi request reprint Clinical characteristics of congenital and developmental cataract undergoing surgical treatment
    Toshiyuki Nagamoto
    Department of Ophthalmology, Kyorin University School of Medicine, Tokyo, Japan
    Jpn J Ophthalmol 59:148-56. 2015
    ..To analyze the clinical characteristics of congenital/developmental cataract undergoing surgery...
  42. pmc Generation of retinal ganglion cells with functional axons from human induced pluripotent stem cells
    Taku Tanaka
    Department of Ophthalmology and Laboratory for Visual Science, National Centre for Child Health and Development, Tokyo, Japan
    Sci Rep 5:8344. 2015
    ....
  43. pmc Human sclera maintains common characteristics with cartilage throughout evolution
    Yuko Seko
    Department of Reproductive Biology and Pathology, National Institute for Child and Health Development, Tokyo, Japan
    PLoS ONE 3:e3709. 2008
    ..The aim of this study is to identify characteristics of the human sclera as one of the connective tissues derived from the neural crest and mesoderm...
  44. doi request reprint Mutation spectrum and phenotypic variation in nine patients with SOX2 abnormalities
    Junichi Suzuki
    1 National Research Institute for Child Health and Development, Department of Molecular Endocrinology, Tokyo, Japan 2 Department of Pediatrics and Child Health, Nihon University School of Medicine, Tokyo, Japan
    J Hum Genet 59:353-6. 2014
    ..Our data provide further evidence for wide phenotypic variation of SOX2 abnormalities and the lack of genotype-phenotype correlation in patients carrying SOX2 lesions. ..
  45. doi request reprint Ophthalmic features of CHARGE syndrome with CHD7 mutations
    Sachiko Nishina
    Division of Ophthalmology, National Center for Child Health and Development, Tokyo, Japan
    Am J Med Genet A 158:514-8. 2012
    ....
  46. doi request reprint SOX10 mutation in Waardenburg syndrome type II
    Manami Iso
    Department of Endocrinology and Metabolism, National Research Institute for Child Health and Development, Tokyo, Japan
    Am J Med Genet A 146:2162-3. 2008
  47. doi request reprint Nishida's procedure combined with medial rectus recession for large-angle esotropia in Duane syndrome
    Michiko Tanaka
    Division of Ophthalmology, National Center for Child Health and Development, 2 10 1 Okura, Setagaya Ku, Tokyo, 157 8535, Japan
    Jpn J Ophthalmol 55:264-7. 2011
    ..Two patients presented large-angle esotropia due to unilatelal Duane syndrome type I...
  48. doi request reprint Is a 6-week course of ganciclovir therapy effective for chorioretinitis in infants with congenital cytomegalovirus infection?
    Kensuke Shoji
    Division of General Pediatrics, Department of Interdisciplinary Medicine, National Center for Child Health and Development, Tokyo, Japan
    J Pediatr 157:331-3. 2010
    ..We report an infant with congenital CMV infection, who required a 6-month course of antiviral therapy to control his chorioretinitis. Long-term treatment may be necessary for managing congenital CMV-associated chorioretinitis...
  49. ncbi request reprint Improvement of skeletal lesions in mice with mucopolysaccharidosis type VII by neonatal adenoviral gene transfer
    Arihiko Kanaji
    National Research Institute of Child Health and Development, 157 8535, Tokyo, Japan
    Mol Ther 8:718-25. 2003
    ....
  50. ncbi request reprint Non-cleavable mutant Fas ligand transfection of donor cornea abrogates ocular immune privilege
    Yoichiro Sano
    Department of Ophthalmology, Kyoto Prefectural University of Medicine, Japan
    Exp Eye Res 75:475-83. 2002
    ..Our results indicate that membrane-binding FasL over expression in donor cornea does not prolong corneal allograft survival; indeed, it causes rapid graft destruction...
  51. ncbi request reprint Detection of cytotoxic anti-LEDGF autoantibodies in atopic dermatitis
    Masahiko Ayaki
    Center for Ophthalmic Research, Brigham and Women s Hospital, Department of Ophthalmology, Harvard Medical School, 221 Longwood Avenue, Boston, MA 02115, USA
    Autoimmunity 35:319-27. 2002
    ....
  52. ncbi request reprint Histological study of the hypertrophic placentas and open eyelids observed in cloned fetuses
    Nobuhiro Shimozawa
    Central Institute for Experimental Animals, Kawasaki, Kanaga, Japan
    J Reprod Dev 49:221-6. 2003
    ....
  53. ncbi request reprint [Problems on treatment of congenital cataract]
    Noriyuki Azuma
    Nihon Ganka Gakkai Zasshi 106:263-4. 2002
  54. ncbi request reprint [Early vitreous surgery for a severe form of retinopathy of prematurity]
    Noriyuki Azuma
    Nihon Ganka Gakkai Zasshi 110:822-9. 2006
  55. ncbi request reprint Small eye phenotypes observed in a human tau gene transgenic rat
    Kazuo Goto
    Central Institute for Experimental Animals, Kawasaki, Japan
    Curr Eye Res 31:107-10. 2006
    ..Cytogenetic analysis suggested that the chromosome location of the transgene was chromosome 1 (1p12). This region may include genes related to lens development, such as Cat5...