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Advances in Vision Research, Volume I : Genetic Eye Research in Asia and the Pacific / / edited by Gyan Prakash, Takeshi Iwata
| Advances in Vision Research, Volume I : Genetic Eye Research in Asia and the Pacific / / edited by Gyan Prakash, Takeshi Iwata |
| Edizione | [1st ed. 2017.] |
| Pubbl/distr/stampa | Tokyo : , : Springer Japan : , : Imprint : Springer, , 2017 |
| Descrizione fisica | 1 online resource (XV, 523 p. 71 illus., 55 illus. in color.) |
| Disciplina | 617.7 |
| Collana | Essentials in Ophthalmology |
| Soggetto topico |
Ophthalmology
Human genetics Human Genetics |
| ISBN | 4-431-56511-6 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | 1. Foundation of Asian Eye Genetics Consortium (AEGC) (Gyan Prakash, Takeshi Iwata) -- 2. Japan consortium for whole exome analysis of hereditary retinal diseases (Takeshi Iwata) -- 3. Whole-genome sequencing in genetic eye diseases in China (Zi-bing Jin) -- 4. Targeted exome sequencing in Japanese patients with Retinitis Pigmentosa (Maho Oishi, Akio Oishi, Nagahisa Yoshimura) -- 5. Genetic Epidemiology of Congenital Cataracts and Autosomal Recessive Retinal Degenerations in Pakistan (Fielding Hejtmancik, Qiwei Wang, Yabin Chen, Sheikh Riazuddin and S. Amer Riazuddin) -- 6. Genetics of Cataract in Asia (Chitra Kannabiran and Vanita) -- 7. Genetic analysis of families with retinal dystrophies (Qingjiong Zhang) -- 8. Whole genome sequencing in patients with Retinitis Pigmentosa (Koji M. Nishiguchi) -- 9. Retinitis pigmentosa in Korean patients (C.K. Yoon, U.C. Park and H.G. Yu) -- 10. Retinitis pigmentosa in Chinese population (Ruifang Sui and Xuan Zou) -- 11. Retinitis Pigmentosa in Japanese Population (Katsuhiro Hosono, Shinsei Minoshima, Yoshihiro Hotta) -- 12. Cone Dysfunction Syndrome in Japanese Population (Takaaki Hayashi) -- 13. Leber Congenital Amaurosis/Early-Onset Retinal Dystrophy in Japanese Population (Kazuki Kuniyoshi and Yoshikazu Shimomura) -- 14. Paradigm of Susceptibility genes in AMD and PCV (Paul N. Baird and Moeen Riaz) -- 15. Genetics and Pathology of Inflammatory Components on AMD (Xiaoxin Li, Lv-Zhen Huang, Peng Zhou and Chi Chao Chan) -- 16. Genome wide association study of age-related eye diseases in Chinese population (Guy L.J. Chen, Shi Song Rong and Calvin C.P. Pang) -- 17. Clinical Genetics of Retinoblastoma: An Asian Perspective (Ashwin Mallipatna and Meghan Marino and Arun Singh) -- 18. Molecular and Clinical Genetics of Retinoblastoma (Jason C.S. Yam, Winnie W. Y. Lau, Wai Kit Chu, L.J. Chen, K. W. Choy, Simon T.C. and Calvin C.P. Pang) -- 19. Current research Perspectives in Understanding Diabetic Retinopathy (A Jayamuruga Pandian, Nagasamy Soumittra, Rajiv Raman, Sarangapani Sripriya) -- 20. Genome-wide association studies of glaucoma (Zachary Dong, Chiea Chuen Khor and Janey L. Wiggs) -- 21. Genetic Complexity of Primary Angle Closure Glaucoma in Asians (Roopam Duvesh, R Venkatesh, S Kavitha, Pradeep Ramulu, SR Krishnadas and P Sundaresan) -- 22. Genotype-phenotype correlation for POAG in the Middle East Khaled Abu-Amero (Saudi Arabia), Alta (A. Kondkar and Ahmed Mousa) -- 23. Corneal Dystrophies in India (Namrata Sharma and Arundhati Sharma) -- 24. Genetics of Corneal Endothelial Dystrophies: An Asian Perspective (Sudha Neelam, Jod Mehta, Eranga Vithana and Vinod Mootha) -- 25. Keratoconus in Asia (Rajiv Mohan, Arkasubhra Ghosh and Rohit Shetty) -- 26. Genetics of Pediatric Eye Diseases and Strabismus in Asia (Zia Chaudhuri and Birgit Lorenz) -- 27. Keratoconus: Globally and in the Middle East; Epidemiology, Genetics and future Research (Ahmed Mousa, Altaf Kondkar and Khaled Abu-Amero) -- 28. Genetics of Myopia (Sushil Kumari Sangwan, Arundhati Sharma, Namrata Sharma, Radhika Tandon) -- 29. Ocular Implications of Gaucher Disease (Mones S. Abu-Asab, Ian Y. L. Yeung, Christopher Ardeljan, Ashley N. Gonzalez, Ellen Sidransky, Chi-Chao Chan) -- 30. Genetic background of Uveitis in Chinese population (Peiziang Yang, Hongsong Yu, Bo Lei and Aize Kijlstra) -- 31. Usher Syndrome in Chinese and Japanese Population (Shi-Ying Li, Linghui Qu, and Xiaohong Meng, and Zheng Qin Yin) -- 32. Homozygosity Mapping for Autosomal Recessive Ocular Diseases (Chandrasekar SatyaPriya, Sundaramoorthy Srilekha, Karthikeyan Sudha, Sarangapani Sripriya, Nagasamy Soumittra) -- 33. Tools of Genetic Eye Research and Need for Clinical Research Collaborations (Vanita Vanita and Umang Mathur) -- 34. Eye Genetics: The Road Ahead to Quality Standards (Sridhar Bammidi, Kaushal Sharma, Rahul Tyagi, Neel Kamal Sharma and Akshay Anand) -- 35. Genetic Counselling in Asia (Viney Gupta and Ken K. Nischal) -- 36. Epigenetic study in Asian Eye Diseases (Lai Wei, Xiao Hu and Xiafeng Wen) -- 37. Unique Asian Patients Population: An Opportunity for Drug Development (Rajkumar Patil, Cheng Ching Yu, Chui Ming Gemmy Cheung and Tien Yin Wong -- 38. A Perspective: How can gene therapeutics help address ophthalmic health issues in Asia? (Paul Kaufman). |
| Record Nr. | UNINA-9910254468603321 |
| Tokyo : , : Springer Japan : , : Imprint : Springer, , 2017 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Advances in Vision Research, Volume II : Genetic Eye Research in Asia and the Pacific / / edited by Gyan Prakash, Takeshi Iwata
| Advances in Vision Research, Volume II : Genetic Eye Research in Asia and the Pacific / / edited by Gyan Prakash, Takeshi Iwata |
| Edizione | [1st ed. 2019.] |
| Pubbl/distr/stampa | Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2019 |
| Descrizione fisica | 1 online resource (464 pages) |
| Disciplina | 617.7042 |
| Collana | Essentials in Ophthalmology |
| Soggetto topico |
Ophthalmology
Medical genetics Medical Genetics |
| ISBN | 981-13-0884-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Foreword -- Chapter 1: Update on Asian Eye Genetics Consortium (AEGC) -- Chapter 2: A Bibliometric Analysis of AEGC Publications -- Chapter 3: Opportunity for population based eye research in Asia and the Middle East: An NGO perspective -- Chapter 4 eyeGENE®: A model for advancing research of rare, inherited eye conditions through biobanking and data sharing -- Chapter 5: Inherited Ocular Disease in the New Zealand Māori; Novel genetic mechanisms and founder effects -- Chapter 6: Genetics of ocular diseases in Malaysia -- Chapter 7: Challenges and Opportunities in Genetic Research from the Perspective of a Tertiary Eye Care Hospital in Bangladesh -- Chapter 8: Genetic Research on Ocular Health and Disease in a Population from Nepal -- Chapter 9: The beginnings of genetic eye research in the Philippines: Case studies and a research center development framework -- Chapter 10: Hereditary Eye Disease in Ningxia Hui Autonomous Region of China -- Chapter 11: Ophthalmic Genetics in India; From Tentative Beginnings in the 1980s to Major Achievements in the 21st century -- Chapter 12: Panel-Based Next-Generation Sequencing for Inherited Retinal Degenerations in Koreans -- Chapter 13: Genetic Disease in Ophthalmology: Health Care and Research Opportunity in Bangladesh -- Chapter 14: Update on Japan Eye Genetics Consortium -- Chapter 15: Genetics and susceptibility of retinal eye diseases in India -- Chapter 16: Unique Patient Populations in Asia for Genetic Eye Research -- Chapter 17: Retina Genes in Chinese -- Chapter 18: Leber Congenital Amaurosis in Asia -- Chapter 19: The genetics of inherited retinal diseases in the Israeli and Palestinian populations: a lesson from populations with high consanguinity levels -- Chapter 20: Occult Macular Dystrophy -- Chapter 21: Adeno-Associated Virus (AAV) Mediated Gene Therapy for Leber Hereditary Optic Neuropathy -- Chapter 22: Stargardt disease in Asian population -- Chapter 23 Retinoblastoma Genes in Chinese Studies -- Chapter 24: Genetics of Retinoblastoma: Basic Research and Clinical Applications -- Chapter 25: Genotype-Phenotype correlation in retinal degenerations -- Chapter 26: Cyp1B1 gene in Primary Congenital Glaucoma" and "Genetic Analysis of LCA in Indonesian patients -- Chapter 27: "Diabetic Retinopathy: Clinical, Genetic and Health Economics-An Asian Perspective" -- Chapter 28: Quantitative Trait for Glaucoma -- Chapter 29: Genetics of Exfoliation Syndrome in Asians -- Chapter 30: Proteomics of Neurodegenerative Disorders of the Eye -- Chapter 31: Genomic Approaches to Eye Diseases: An Asian Perspective -- Chapter 32: Myopia genes in Asians -- Chapter 33: Keratoconus Genes in Chinese -- Chapter 34 Granular corneal dystrophy type 2: Prevalence in Korea, Molecular Cell Biology and trials for the treatment -- Chapter 35: Glaucoma Genes in East Asian Studies -- Chapter 36: Clinical Genetics of Vitelliform Macular Dystrophy: An Asian Perspective. |
| Record Nr. | UNINA-9910350239203321 |
| Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2019 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Advances in Vision Research, Volume III : Genetic Eye Research around the Globe / / edited by Gyan Prakash, Takeshi Iwata
| Advances in Vision Research, Volume III : Genetic Eye Research around the Globe / / edited by Gyan Prakash, Takeshi Iwata |
| Edizione | [1st ed. 2021.] |
| Pubbl/distr/stampa | Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2021 |
| Descrizione fisica | 1 online resource (478 pages) : illustrations |
| Disciplina | 617.7 |
| Collana | Essentials in Ophthalmology |
| Soggetto topico |
Ophthalmology
Medical genetics Medical Genetics |
| ISBN | 981-15-9184-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | 1. Expansion of Asian Eye Genetics Consortium (AEGC) to Global Eye Genetics Consortium (GEGC), Introduction of a global Phenotype-Genotype Database “GenEye” and Launch of New Training Programs at National Eye Institute (NEI) -- 2. Global Women’s Eye Health: a Genetic Epidemiologic perspective -- 3. Establishing the Chinese Arm of GEGC -- 4. Human material for research: Eye banking, biobanking and ethical access -- 5. Current Understanding of Polypoidal Choroidal Vasculopathy -- 6. Genetics of Age-related macular degeneration (AMD) in Asia -- 7. The contribution of rare allele and Junk Genome in AMD pathogenesis -- 8. Differential genotypes in age-related macular degeneration and polypoidal choroidal vasculopathy: a updated meta-analysis -- 9. Genetic Epidemiology of Quantitative Traits of Primary Open Angle Glaucoma -- 10. Association studies on retina diseases in Chinese population -- 11. Congenital stationary night blindness (CSNB) – an inherited retinal disorder where clear correlations can be made -- 12. Genome analysis for inherited retinal disease: the state of the art -- 13. Generation and analysis of induced photoreceptor-like cells from fibroblasts of patients with retinitis pigmentosa -- 14. Genotype-phenotype of RPE65 mutations: A reference guide for gene testing and its clinical application -- 15. Genetic variants and impact in PDE6B rod-cone dystrophy -- 16. The retinitis pigmentosa genes -- 17. Primary Congenital Glaucoma Genetics – The Experience in Brazil -- 18. Glaucoma genetics in Pakistan -- 19. Contributions of Promoter Variants to Complex Eye Diseases -- 20. Vascular Basement Membrane Thickening – Basis of disease pathology in diabetic retinopathy -- 21. Molecular Genetics and Clinical aspects of Macular Corneal Dystrophy -- 22. Congenital and Inherited Cataracts -- 23. Higher order aberrations: differences among populations from various demographics -- 24. Genetics Of Microphthalmia: Global And Indian Perspectives -- 25. Regional Differences in Prevalence of Myopia: Genetic or Environmental Effects? -- 26. Consortium for Refractive Error and Myopia (CREAM): Vision, Mission and Accomplishments -- 27. Oncologic properties of retinoblastoma genes -- 28. Oncologic implications of genetic and epigenetic basis of pterygium -- 29. The need for alternative therapies in eye disorders -- 30. Gene Therapy and Retinal Disease -- 31. The use of human pluripotent stem cells (hPSCs) and CRISPR-mediated gene editing in retinal diseases. |
| Record Nr. | UNINA-9910484613303321 |
| Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2021 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Advances in Vision Research, Volume IV : From Basic to Translational Research — Developing Diagnostics and Therapeutics for Genetic Eye Diseases / / edited by Gyan Prakash, Takeshi Iwata
| Advances in Vision Research, Volume IV : From Basic to Translational Research — Developing Diagnostics and Therapeutics for Genetic Eye Diseases / / edited by Gyan Prakash, Takeshi Iwata |
| Autore | Prakash Gyan |
| Edizione | [1st ed. 2024.] |
| Pubbl/distr/stampa | Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024 |
| Descrizione fisica | 1 online resource (393 pages) |
| Disciplina | 617.7 |
| Altri autori (Persone) | IwataTakeshi |
| Collana | Essentials in Ophthalmology |
| Soggetto topico |
Ophthalmology
Medical genetics Stem cells Medical Genetics Stem Cell Biology |
| ISBN |
9789819944361
9789819944354 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Part I Gene therapy for ocular genetic diseases -- Chapter 1 Gene therapy for neovascular age-related macular degeneration -- Chapter 2 Gene therapy trial on X-linked retinitis pigmentosa caused by mutations in RPGR -- Chapter 3 Optogenetic approaches to restore vision -- Chapter 4 Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis -- Chapter 5 Subretinal versus Intravitreal Delivery of AAV8 in Nonhuman Primates -- Chapter 6 Gene therapy for Leber Congenital Amaurosis caused by mutation in RPE65 -- Chapter 7 Release of rAAV Vectors from APMA-Functionalized Contact Lenses for Corneal Gene Therapy -- Chapter 8 Gene Therapy to Prevent Retinal Ganglion Cell Loss in Glaucoma and Leber’s Hereditary Optic Neuropathy -- Part II Gene editing as therapy for ocular disease -- Chapter 9 Gene Therapy for Glaucoma by Ciliary Body Aquaporin 1 Disruption Using CRISPR-Cas9 -- Chapter 10 Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 in Mouse and Macaque -- Chapter 11 In Vivo CRISPR/Cas9-Mediated Genome Editing Mitigates Photoreceptor Degeneration in Mouse Model of X-Linked Retinitis Pigmentosa -- Chapter 12 Gene Expression and Editing in Mammalian Retinal Ganglion Cells -- Chapter 13 AAV-mediated mutation replacement genome editing in photoreceptors restores vision in mice -- Chapter 14 Gene Editing Preserves Visual Functions in a Mouse Model of Retinal Degeneration -- Chapter 15 Genome Editing as Treatment for Autosomal Dominant Retinitis Pigmentosa -- Chapter 16 CRISPR/Cas base editors to target the AMD high-risk variant -- Part III Cell therapy for ocular genetic diseases -- Chapter 17 Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration -- Chapter 18 Transplantation Retinal Sheet Differentiated from Patient iPS Cells with Inherited Retinitis Pigmentosa -- Chapter 19 Clinical study of an ES cell-derived retinal pigment epithelium patch in age-related macular degeneration -- Chapter 20 Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients -- Chapter 21 Preclinical safety studies of human embryonic stem cell-derived retinal pigment epithelial cells for the treatment of age-related macular degeneration -- Chapter 22 Corneal endothelial cell derivation methods from ES and iPS cells -- Chapter 23 Gene editing approach to restore vision loss in Leber Congenital Amaurosis type 10 -- Chapter 24 Inhibition of Optineurin – TANK Binding Kinase 1 interaction to suppress inherited normal tension glaucoma -- Chapter 25 A 3D Printed Self-Sustainable Cell-Encapsulation Drug Delivery Device for Periocular Transplant-Based Treatment of Retinal Degenerative Diseases -- Chapter 26 Complement inhibition as therapy for retinal diseases -- Chapter 27 Neuroprotective Therapy for Retinal Ganglion Cell Degeneration -- Chapter 28 Artificial intelligence in retina -- Chapter 29 Prediction of AI for Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis -- Chapter 30 Artificial Intelligence for Evaluation of Macular Degeneration and Suspected Glaucoma -- Chapter 31 Artificial Intelligence Classification of Central Visual Field Patterns in Glaucoma -- Chapter 32 Artificial intelligence and deep learning in ophthalmology. |
| Record Nr. | UNINA-9910865282103321 |
Prakash Gyan
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| Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||