標(biāo)題: Titlebook: Genetics of Ocular Diseases; H. V. Nema,Nitin Nema Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license to S [打印本頁] 作者: papyrus 時(shí)間: 2025-3-21 17:01
書目名稱Genetics of Ocular Diseases影響因子(影響力)
書目名稱Genetics of Ocular Diseases影響因子(影響力)學(xué)科排名
書目名稱Genetics of Ocular Diseases網(wǎng)絡(luò)公開度
書目名稱Genetics of Ocular Diseases網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Genetics of Ocular Diseases被引頻次
書目名稱Genetics of Ocular Diseases被引頻次學(xué)科排名
書目名稱Genetics of Ocular Diseases年度引用
書目名稱Genetics of Ocular Diseases年度引用學(xué)科排名
書目名稱Genetics of Ocular Diseases讀者反饋
書目名稱Genetics of Ocular Diseases讀者反饋學(xué)科排名
作者: 逗留 時(shí)間: 2025-3-21 20:23 作者: 壓倒 時(shí)間: 2025-3-22 00:43
Die Pathologie des Herzstoffwechsels,l scarring. It commonly occurs as an isolated disease but is known to be associated with other ocular and systemic disorders. Genetic component in the etiology of keratoconus is well recognized with contribution from environmental and more recently, inflammatory factors. Multiple approaches have bee作者: 聽寫 時(shí)間: 2025-3-22 05:58
https://doi.org/10.1007/978-3-531-91867-9Disease (DED). Therefore, the environmental and genetic risk factors for developing DED are multiple and diverse..The spectrum of DED includes both evaporative and aqueous deficient forms, with a combined form predominating in most cases.作者: Pigeon 時(shí)間: 2025-3-22 12:25
,Die Stabilit?t der Befehlsketten,different routes of administration of gene therapy. Embryology of the lens starts with the neuroectoderm stimulating the thickened surface ectoderm with transcription factors including PAX 6, Sox2, and Six3 gene to form the lens placode. The invagination later leads to the formation of the lens pit 作者: Conscientious 時(shí)間: 2025-3-22 13:15
https://doi.org/10.1007/978-3-658-07758-7e in one’s life. Glaucoma, characterized by progressive damage to retinal ganglion cells (RGCs) and concomitant visual field loss is the leading cause of irreversible blindness globally. People from all the age groups can be affected by the varying glaucoma subtypes with either Mendelian or complex 作者: Conscientious 時(shí)間: 2025-3-22 19:33 作者: LAY 時(shí)間: 2025-3-23 01:05 作者: MULTI 時(shí)間: 2025-3-23 03:33 作者: Friction 時(shí)間: 2025-3-23 07:38 作者: ALOFT 時(shí)間: 2025-3-23 10:05
https://doi.org/10.1007/978-3-476-02750-4own, there is a substantial amount of research that demonstrates a link between various heritable factors and the pathogenesis of this disease. Currently, most of the literature available discusses the role of genes in syndromic forms of RRD (Stickler–Wagner syndrome). In addition, there is some lim作者: Urea508 時(shí)間: 2025-3-23 14:38 作者: 憤怒歷史 時(shí)間: 2025-3-23 20:34
https://doi.org/10.1007/978-3-663-06960-7ious blinding conditions like macular degeneration, retinal detachment, glaucoma, and cataract. High myopia has a complex heterogeneous aetiology including environmental and genetic factors and is still not thoroughly understood. Till date, over 100 genes and more than 20 chromosomal loci, which are作者: 藥物 時(shí)間: 2025-3-23 22:19 作者: Arrhythmia 時(shí)間: 2025-3-24 04:03
https://doi.org/10.1007/978-3-663-20182-3erised by the dysfunction of neuronal and vascular parts of the retina and eventually progresses to the proliferative stage. Current treatment strategies hold good support in reducing this burden, but they are not effective in the early stages and induces side effects. This demands for targeting tow作者: 傀儡 時(shí)間: 2025-3-24 09:38
Massenmedien und Massenkommunikationrate diagnosis and personalised management. The genetic counseling process should adhere to some basic ethical principles and be carried out in such a manner, that the patient and family receive adequate information as well as the necessary support. During counseling, the patient’s diagnosis and inh作者: homeostasis 時(shí)間: 2025-3-24 10:42 作者: Scintigraphy 時(shí)間: 2025-3-24 17:52
H. V. Nema,Nitin NemaIncludes a separate chapter on genetic counselling in eye diseases with the help of examples.Discusses recent trends in gene therapy of eye diseases.Written by well-known ophthalmologists and genetici作者: 變色龍 時(shí)間: 2025-3-24 20:55 作者: botany 時(shí)間: 2025-3-24 23:17 作者: hemorrhage 時(shí)間: 2025-3-25 05:58
https://doi.org/10.1007/978-3-531-91867-9Disease (DED). Therefore, the environmental and genetic risk factors for developing DED are multiple and diverse..The spectrum of DED includes both evaporative and aqueous deficient forms, with a combined form predominating in most cases.作者: indifferent 時(shí)間: 2025-3-25 08:37
Genetics in Corneal Dystrophy,s the IC3D classification of corneal dystrophies. This chapter deals with in depth details of inheritance and genetics of corneal dystrophies at nucleotide and amino acid levels. Gene editing being the latest mode of research in gene therapy for the treatment of dystrophies has been described.作者: Astigmatism 時(shí)間: 2025-3-25 12:43
Genetics of Dry Eye Disease,Disease (DED). Therefore, the environmental and genetic risk factors for developing DED are multiple and diverse..The spectrum of DED includes both evaporative and aqueous deficient forms, with a combined form predominating in most cases.作者: Celiac-Plexus 時(shí)間: 2025-3-25 17:28 作者: 凝視 時(shí)間: 2025-3-25 23:16 作者: 生命層 時(shí)間: 2025-3-26 02:17
An Overview on the Genetic Etiology, Testing, and Therapeutic Options for Retinitis Pigmentosa,ations. It also highlights the importance of next-generation sequencing using targeted panel, whole exome, and genome sequencing in the identification of disease-causing variants and differential diagnosis in RP families. The genetic diagnosis has paved the way not only for future gene therapy trial作者: 健談的人 時(shí)間: 2025-3-26 07:52 作者: Integrate 時(shí)間: 2025-3-26 10:34 作者: 帶來 時(shí)間: 2025-3-26 16:39 作者: Creditee 時(shí)間: 2025-3-26 20:53
https://doi.org/10.1007/978-3-658-07758-7PCG along with the sporadic cases. PCG accounts for 5% of blindness in childhood worldwide with variable reported incidence owing to diverse ethnic population and consanguinity status. A large spectrum of data from several genetic studies globally further prompts researchers to look for potential co作者: Cloudburst 時(shí)間: 2025-3-26 23:45
https://doi.org/10.1007/978-3-642-94546-5ations. It also highlights the importance of next-generation sequencing using targeted panel, whole exome, and genome sequencing in the identification of disease-causing variants and differential diagnosis in RP families. The genetic diagnosis has paved the way not only for future gene therapy trial作者: Nomogram 時(shí)間: 2025-3-27 02:01 作者: 直覺沒有 時(shí)間: 2025-3-27 08:52 作者: 獨(dú)特性 時(shí)間: 2025-3-27 13:08
nosis of genetic eye diseases as well as help the geneticists in understaning the basic concepts. It will also be useful for students who are preparing for MD, MS, DNB and FRCS examinations..978-981-16-4249-4978-981-16-4247-0作者: dearth 時(shí)間: 2025-3-27 14:19
Principles of Genetic Counseling in Eye Diseases, manner, that the patient and family receive adequate information as well as the necessary support. During counseling, the patient’s diagnosis and inheritance patterns should be considered. Information about the available molecular testing, management options and prenatal testing should be explained.作者: 可用 時(shí)間: 2025-3-27 21:43 作者: Narcissist 時(shí)間: 2025-3-28 00:51
Genetics in Age-Related Macular Degeneration,less of the immense genetic information discovered so far, diagnostic genetic or biomarker tests are still unavailable to aid in clinical management. Herein we review the advances made in genetics in AMD so far.作者: NICHE 時(shí)間: 2025-3-28 03:33
Die Pathologie des Herzstoffwechsels,n taken to study the role of genetics in the causation of keratoconus including twin studies, familial associations, linkage studies, and genome-wide analysis. This chapter aims to comprehensively describe the studies that provide evidence for the role of genetics in keratoconus which is a common yet etiologically a complex disease.作者: BLANK 時(shí)間: 2025-3-28 08:33
Michael Haller,Martin Niggeschmidtapter discusses the various genes including myocilin and optineurin which are associated with glaucoma, the process of identification, the strength of association and their future role in therapeutics.作者: 漂泊 時(shí)間: 2025-3-28 12:51 作者: CODA 時(shí)間: 2025-3-28 18:17
Genetics of Keratoconus,n taken to study the role of genetics in the causation of keratoconus including twin studies, familial associations, linkage studies, and genome-wide analysis. This chapter aims to comprehensively describe the studies that provide evidence for the role of genetics in keratoconus which is a common yet etiologically a complex disease.作者: 勾引 時(shí)間: 2025-3-28 20:21 作者: 柱廊 時(shí)間: 2025-3-28 23:44 作者: 驚呼 時(shí)間: 2025-3-29 06:49 作者: critique 時(shí)間: 2025-3-29 11:02
https://doi.org/10.1007/978-3-322-98843-0t out and replace a small region of a gene with the mutation, without the need for replacing the entire gene. These advances are in an experimental stage and should enable a tailor-made approach to therapy such that patient-specific editing tools are designed for repair of a single mutation in the gene of interest.作者: 滑稽 時(shí)間: 2025-3-29 11:33 作者: 不規(guī)則 時(shí)間: 2025-3-29 17:10 作者: vascular 時(shí)間: 2025-3-29 21:15 作者: upstart 時(shí)間: 2025-3-30 00:17
Genes and Genetics in Ophthalmology,t out and replace a small region of a gene with the mutation, without the need for replacing the entire gene. These advances are in an experimental stage and should enable a tailor-made approach to therapy such that patient-specific editing tools are designed for repair of a single mutation in the gene of interest.作者: chandel 時(shí)間: 2025-3-30 05:06 作者: 前奏曲 時(shí)間: 2025-3-30 10:33 作者: malign 時(shí)間: 2025-3-30 15:07 作者: Cardiac 時(shí)間: 2025-3-30 20:27 作者: 污點(diǎn) 時(shí)間: 2025-3-31 00:32
Massenmedien und Massenkommunikation manner, that the patient and family receive adequate information as well as the necessary support. During counseling, the patient’s diagnosis and inheritance patterns should be considered. Information about the available molecular testing, management options and prenatal testing should be explained.作者: PURG 時(shí)間: 2025-3-31 01:06
Book 2022have been detected and incriminated in complex mechanisms of causing leading eye diseases such as cataract and glaucoma. This book written by well-established ophthalmologists and geneticists presents a complicated subject in simple and easy to understand manner. Chapters cover the concept of gene t作者: 粗野 時(shí)間: 2025-3-31 07:46 作者: 替代品 時(shí)間: 2025-3-31 12:05
Genetics in Corneal Dystrophy,s the IC3D classification of corneal dystrophies. This chapter deals with in depth details of inheritance and genetics of corneal dystrophies at nucleotide and amino acid levels. Gene editing being the latest mode of research in gene therapy for the treatment of dystrophies has been described.作者: STERN 時(shí)間: 2025-3-31 14:46
