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Advances in Circular RNAs : The Basis and Disease Relevance / / edited by Junjie Xiao
| Advances in Circular RNAs : The Basis and Disease Relevance / / edited by Junjie Xiao |
| Autore | Xiao Junjie |
| Edizione | [1st ed. 2025.] |
| Pubbl/distr/stampa | Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2025 |
| Descrizione fisica | 1 online resource (944 pages) |
| Disciplina | 616.042 |
| Altri autori (Persone) | Xiao |
| Collana | Advances in Experimental Medicine and Biology |
| Soggetto topico |
Medical genetics
Biochemistry Cytology Medical Genetics Cell Biology |
| ISBN | 981-9694-28-0 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Part I: Overview -- Chapter 1: An Overview of Circular RNAs -- Chapter 2: Guidelines for the naming of circular RNAs -- Part II: Bioinformatics for Circular RNAs -- Chapter 3: Circular RNA detection and bioinformatic analysis -- Chapter 4: Online databases in circular RNAs -- Chapter 5: Prediction of circular RNA secondary structures and their targets -- Chapter6: Circular RNA Identification and Characterization with CircRNAFlow: A Bioinformatics Approach -- Part III: Biogenesis of Circular RNAs -- Chapter 7: The formation of circular RNAs -- Chapter 8: RNA binding proteins (RBPs) and circular RNA biogenesis -- Chapter 9: The internal ribosome entry site in circular RNAs -- Part IV: Molecular Mechanisms and Gene Regulation of Circular RNAs -- Chapter 10: Circular RNAs binding to RNA-Binding Proteins -- Chapter 11: Circular RNAs regulate transcription and translation -- Part V: Circular RNAs as Potential Disease Biomarkers -- Chapter 12: Circular RNA in Exosomes and its clinical significance -- Chapter 13: Circular RNAs in Blood and its clinical relevance -- Chapter 14: Circular RNAs as Biomarkers in the diagnosis of Human Diseases -- Chapter 15: Circular RNAs as Novel Biomarkers and application in cardiovascular diseases -- Chapter 16: Circular RNAs synthesis and applications.-Part VI: Circular RNAs and Human Diseases -- Chapter 17: Circular RNAs in heart diseases -- Chapter 18: Circular RNAs in cancers -- Chapter 19: Circular RNAs in organ fibrosis -- Chapter 20: Circular RNAs in metabolic diseases -- Chapter 21: Circular RNAs in liver diseases -- Chapter 22: Circular RNAs in respiratory diseases -- Chapter 23: Circular RNAs in brain physiology and neurologic diseases -- Chapter 24: Circular RNAs in immune-related diseases -- Chapter 25: Circular RNAs in musculoskeletal diseases -- Part VII: Circular RNAs in Archaea -- Chapter 26: Circular RNAs in Archaea. |
| Record Nr. | UNINA-9911022457103321 |
Xiao Junjie
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| Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2025 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Advances in Nutrition and Cancer / / edited by Vincenzo Zappia, Salvatore Panico, Gian Luigi Russo, Alfredo Budillon, Fulvio Della Ragione
| Advances in Nutrition and Cancer / / edited by Vincenzo Zappia, Salvatore Panico, Gian Luigi Russo, Alfredo Budillon, Fulvio Della Ragione |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 |
| Descrizione fisica | 1 online resource (450 p.) |
| Disciplina |
616.99
616.99/4071 616.994071 |
| Collana | Cancer Treatment and Research |
| Soggetto topico |
Oncology
Medicine, Preventive Health promotion Epidemiology Medicine - Research Biology - Research Medical genetics Diseases Health Promotion and Disease Prevention Biomedical Research Medical Genetics |
| ISBN | 3-642-38007-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Part I: Life Style, Diet and Cancer: The role of metabolic carcinogenesis in cancer causation and prevention: evidence from the European prospective investigation into cancer and nutrition -- Obesity, energy balance and cancer: a mechanistic perspective -- Fruits and vegetables. Updating the epidemiologic evidence for the WCRF-AICR lifestyle recommendations for cancer prevention -- The diet as a cause of human prostate cancer -- Mediterranean dietary pattern and chronic diseases -- Dietary salt intake and risk of gastric cancer -- Alcoholic beverages and carbonated soft drinks: consumption and gastrointestinal cancer risks -- Part II: Natural Dietary Molecules: Anti-inflammatory and anti-cancer drugs from nature -- Selenium and cancer: a story that should not be forgotten – Insights from genomics -- Resveratrol: from basic studies to bedside -- Quercetin: a pleiotropic kinase inhibitor against cancer -- Sulforaphane as a promising molecule for fighting cancer -- Part III: Genetics and Epigenetics: Functions, aberrations and advances for chromatin modulation in cancer -- Epigenetics and epidemiology: models of study and examples -- Dietary epigenetics in cancer and aging -- Breast cancer and the importance of early life nutrition -- Part IV: Olive Oil in Cancer Prevention -- Olive oil and other dietary lipids in breast cancer -- A holistic approach to study the effects of natural antioxidants on inflammation and liver cancer -- Extra virgin olive oil: from composition to ‘molecular fastronomy’ -- Part V: Life Style Prevention of Cancer: Life style prevention of cancer recurrence: the yin and the yang -- Part VI: Emerging Breakthroughs: New perspective for an old antidiabetic drug: metformin as anticancer agent -- Gut microbes, diet and cancer -- Inflammatory angiogenesis and the tumor microenvironment as targets for cancer therapy and prevention -- Nutriomes and personalised nutrition for DNA damage prevention, telomere integrity maintenance and cancer growth control -- Novel approaches in melanoma prevention and therapy -- Concluding remarks. |
| Record Nr. | UNINA-9910300071903321 |
| Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Advances in Precision Nutrition, Personalization and Healthy Aging / / edited by Alexander G. Haslberger
| Advances in Precision Nutrition, Personalization and Healthy Aging / / edited by Alexander G. Haslberger |
| Autore | Haslberger Alexander G. |
| Edizione | [1st ed. 2022.] |
| Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2022 |
| Descrizione fisica | 1 online resource (302 pages) |
| Disciplina | 612.67 |
| Collana | Biomedical and Life Sciences Series |
| Soggetto topico |
Nutrition
Aging Medical genetics Ageing Medical Genetics |
| ISBN |
9783031101533
9783031101526 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Foreword -- 1. Trends in personalised precision nutrition, Objectives -- 2. Individualization, precision nutrition developments for the 21st Century -- 3. Precision nutrition from the view of genetics and epigenetics -- 4. Precision Nutrition fromThe View of the Gut Microbiome -- 5. Personalised nutrition for healthy aging, a review -- 6. Precise Nutrition and Metabolic Syndrome, remodeling the Microbiome with Polyphenols, Probiotics and Postbiotics -- 7. Precision nutrition and metabolomics, a model of Alzheimer’s Disease -- 8. Precision nutrition and cognitive decline -- 9. Algorithms for the analysis of markers in personalized health care -- 10. Precise Nutrition and Functional Foods -- 11. Precision nutrition from a practical clinical view, a case study -- 12. Translational aspects in Precision Nutrition, Personalization, Bio-Markers and Healthy Aging. |
| Record Nr. | UNINA-9910629286503321 |
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Haslberger Alexander G.
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| Cham : , : Springer International Publishing : , : Imprint : Springer, , 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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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 | ||
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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 | ||
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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 |
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Prakash Gyan
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| Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Assessing Rare Variation in Complex Traits : Design and Analysis of Genetic Studies / / edited by Eleftheria Zeggini, Andrew Morris
| Assessing Rare Variation in Complex Traits : Design and Analysis of Genetic Studies / / edited by Eleftheria Zeggini, Andrew Morris |
| Autore | Ritchie Graham |
| Edizione | [1st ed. 2015.] |
| Pubbl/distr/stampa | New York, NY : , : Springer New York : , : Imprint : Springer, , 2015 |
| Descrizione fisica | 1 online resource (262 p.) |
| Disciplina | 610 |
| Soggetto topico |
Medical genetics
Medicine - Research Biology - Research Biometry Medical Genetics Biomedical Research Biostatistics |
| ISBN | 1-4939-2824-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Calling Rare Variants from Genotype Data -- Calling Variants from Sequence Data -- Rare Variant Quality Control -- Rare Structural Variants -- Functional Annotation of Rare Genetic Variants -- The 1000 Genomes Project -- The UK10K Project -- Population Isolates -- Natural Selection at Rare Variants -- Collapsing Approaches for the Association Analysis of Rare Variants -- Rare Variant Association Analysis: Beyond Collapsing Approaches -- Significance Thresholds for Rare Variant Signals -- Power of Rare Variant Aggregate Tests -- Replicating Sequence-based Association Studies of Rare Variants -- Meta-analysis of Rare Variants -- Population Stratification of Rare Variants -- Use of Appropriate Controls in Rare Variant Studies -- Trans-ethnic Fine-mapping of Rare Causal Variants. |
| Record Nr. | UNINA-9910298455103321 |
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Ritchie Graham
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| New York, NY : , : Springer New York : , : Imprint : Springer, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Atlas of Inherited Retinal Diseases / / edited by Stephen H. Tsang, Tarun Sharma, Vlad Diaconita
| Atlas of Inherited Retinal Diseases / / edited by Stephen H. Tsang, Tarun Sharma, Vlad Diaconita |
| Autore | Tsang Stephen H |
| Edizione | [2nd ed. 2025.] |
| Pubbl/distr/stampa | Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2025 |
| Descrizione fisica | 1 online resource (433 pages) |
| Disciplina | 617.735 |
| Altri autori (Persone) |
SharmaTarun
DiaconitaVlad |
| Collana | Advances in Experimental Medicine and Biology |
| Soggetto topico |
Ophthalmology
Medical genetics Genetics Clinical Genetics Medical Genetics Genetics and Genomics |
| ISBN | 3-031-72230-2 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Chapter 1 Retinal Histology and Anatomical Landmarks -- Chapter 2 Fluorescein Angiography -- Chapter 3 Optical Coherence Tomography -- Chapter 4 Fundus Autofluorescence -- Chapter 5 ERG -- Chapter 6 Electrooculography -- Chapter 7 Glossary of Relevant Genetic and MolecularCell Biology -- Chapter 8 X-linked Retinitis Pigmentosa -- Chapter 9 X-linked Choroideremia -- Chapter 10 X-linked Juvenile Retinoschisis -- Chapter 11 X-linked Ocular Albinism -- Chapter 12 Progressive Cone Dystrophy and Cone-Rod Dystrophy -- Chapter 13 Congenital Stationary Night Blindness -- Chapter 14 Blue Cone Monochromatism -- Chapter 15 Autosomal Dominant Retinitis Pigmentosa -- Chapter 16 Best Vitelliform Macular Dystrophy -- Chapter 17 Pattern Dystrophy -- Chapter 18 Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese, Autosomal Dominant Drusen) -- Chapter 19 Occult Macular Dystrophy -- Chapter 20 Sorsby Pseudoinflammatory Fundus Dystrophy -- Chapter 21 North Carolina Macular Dystrophy -- Chapter 22 Pigmented Paravenous Chorioretinal Atrophy (PPCRA) -- Chapter 23 Late-Onset Retinal Degeneration -- Chapter 24 Achromatopsia (Rod Monochromatism) -- Chapter 25 Retinitis Pigmentosa (Non-syndromic) -- Chapter 26 Leber Congenital Amaurosis -- Chapter 27 Stargardt Disease -- Chapter 28 Enhanced S-Cone Syndrome (Goldmann-Favre Syndrome) -- Chapter 29 Best Vitelliform Macular Dystrophy -- Chapter 30 Mitochondrial Disorder Kearns-Sayre Syndrome -- Chapter 31 MIDD -- Chapter 32 Usher Syndrome -- Chapter 33 Bardet-Biedl Syndrome -- Chapter 34 Senior-Loken Syndrome -- Chapter 35 Alstrom Syndrome. Chapter 36 Sjogren-Larsson Syndrome -- Chapter 37 Inborn Errors of Metabolism Gyrate Atrophy -- Chapter 38 Pseudoxanthoma Elasticum -- Chapter 39 Refsum Disease -- Chapter 40 Bietti -- Chapter 41 Alport Syndrome -- Chapter 42 N - Stickler Syndrome -- Chapter 43 N - OTX2 Syndrome -- Chapter 44 VHL -- Chapter 45 Tuberous Sclerosis -- Chapter 46 Neurofibromatosis -- Chapter 47 Rubella Retinopathy -- Chapter 48 Syphilis -- Chapter 49 AIR -- Chapter 50 Drug-Induced Retinal Toxicity -- Chapter 51 Non-Infectious Uveitis -- Chapter 52 Diffuse Unilateral Subacute Neuroretinitis (DUSN) -- Chapter 53 CSCR -- Chapter 54 Pathologic Myopia -- Chapter 55 A Practical Approach to Retinal Dystrophies -- Chapter 56 Genetic Testing For Inherited Retinal Dystrophy -- Chapter 57 Genetic Reports -- Chapter 58 The genetic basis of IRDS and the role of genetic testing -- Chapter 59 Seeing Stars The Gene Therapy Revolution -- Chapter 60 Mutation Specific Treatments for Inherited Retinal Diseases -- Chapter 61 Global Treatment Approaches Part 1 Neuroprotection and Stem Cell Therapy -- Chapter 62 Global Treatment Approaches Part 2 Optogenetics and Retinal Implants. |
| Record Nr. | UNINA-9911018751303321 |
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Tsang Stephen H
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| Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2025 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Biochemical Mechanisms for Metabolic Syndrome / / edited by Tejal Gandhi, Anita Mehta
| Biochemical Mechanisms for Metabolic Syndrome / / edited by Tejal Gandhi, Anita Mehta |
| Autore | Gandhi Tejal |
| Edizione | [1st ed. 2024.] |
| Pubbl/distr/stampa | Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2024 |
| Descrizione fisica | 1 online resource (586 pages) |
| Disciplina | 572.4 |
| Altri autori (Persone) | MehtaAnita |
| Collana | Advances in Biochemistry in Health and Disease |
| Soggetto topico |
Metabolism
Metabolism - Disorders Biochemistry Cytology Medical genetics Medical microbiology Metabolic Disease Metabolic Pathways Medical Genetics Medical Microbiology |
| ISBN | 9783031756863 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Part I: Overview and Introduction to Metabolic Syndrome -- 1. The biochemical symphony of metabolic syndrome: An intricate introduction -- 2. Insulin resistance and its biochemical basis in metabolic syndrome -- 3. Lipid metabolism dysregulation: Impact on metabolic syndrome -- 4. The weighty impact: Exploring the importance of obesity in metabolic Syndrome -- 5. Connecting the dots: The complex relationship between metabolic syndrome and hypertension -- 6. The orchestra of genetics: Genetic predisposition to metabolic syndrome Prachi Kariaa and Kirti Patela -- Part II: Cellular and Tissue Mechanisms in Metabolic Syndrome -- 7. cGAS-STING: A regulator of intestinal barrier dysfunction and metabolic syndrome -- 8. Adipose tissue remodeling and metabolic syndrome progression -- 9. Mitochondrial dysfunction, metabolic syndrome and the Pathogenesis of Metabolic Diseases -- Part III. Emerging Molecular Mechanisms and Signaling Pathways -- 10. Inflammatory resolution and its relevance to metabolic syndrome -- 11. Role of Brain Natriuretic Peptide in Metabolic and Hypertrophic Heart Failure -- 12. Endoplasmic reticulum stress and unfolded protein response in metabolic syndrome -- 13. The Impact of Nrf2 Signalling Pathway in Redox Regulation, Inflammation Attenuation, and Management of Metabolic Syndrome: A Systematic Review -- Part IV. Brain-Gut-Adipose Axis and Endocrine Regulation -- 14. Gut Microbiota-derived metabolites and their impact on Obesity -- 15. The Impact of Gut Hormones and the Gut-Adipose-Liver Axis in Metabolic Syndrome: An Overview of Nrf2 Involvement in the Signaling Pathways -- 16. Neuronal regulation of thermogenesis and energy expenditure in Metabolic syndrome -- 17. Endocrine interplay in metabolic syndrome -- Part V. Omics Technologies: Unraveling the Molecular Complexity of Metabolic Syndrome -- 18. Understanding Cardiometabolic Diseases through Transcriptomic approach -- Part VI. Current Therapies and Future Perspectives of Metabolic Syndrome -- 19. Metabolic Syndrome Management through Omega-3 polyunsaturated fatty acids and Antioxidant-Rich Diets: An Approach from Marine and Vegetarian Sources -- 20. Pharmacological Interventions of Metabolic Syndrome -- 21. Metabolic syndrome and associated cognitive dysfunction: a pharmacological perspective -- 22. Brown adipose tissue and its therapeutic potential for Metabolic Syndrome -- 23. Bariatric Surgery and Metabolic Syndrome -- 24. Complementary and Alternative medicine in Metabolic Syndrome Management -- 25. Future Directions and Emerging Research in Metabolic syndrome. |
| Record Nr. | UNINA-9910918693403321 |
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Gandhi Tejal
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| Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2024 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Biomarkers in Dermatology / / edited by Robert Norman
| Biomarkers in Dermatology / / edited by Robert Norman |
| Autore | Norman Robert |
| Edizione | [1st ed. 2025.] |
| Pubbl/distr/stampa | Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2025 |
| Descrizione fisica | 1 online resource (383 pages) |
| Disciplina | 610.28 |
| Altri autori (Persone) | Norman |
| Soggetto topico |
Dermatology
Internal medicine Medical genetics Internal Medicine Medical Genetics |
| ISBN |
9783031665134
3031665139 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Mitochondrial DNA biomarkers in skin disease featuring skin aging -- Serum Biomarkers in Dermatology -- Biomarkers in Psoriasis -- Biomarkers in Atopic Dermatitis -- Biomarkers in cutaneous keratinocyte carcinomas -- Skin Biomarkers of Neurodegenerative Diseases -- Defining Diagnosis in Neurodegeneration through the Search of Biomarkers in Skin -- Skin Biomarker in Parkinson Disease -- Biomarkers in Merkel Cell Carcinoma -- Biomarkers in Melanoma -- Biomarkers in Hidradenitis Suppurativa -- Biomarkers in Wound Healing -- Biomarkers in Acne & Rosacea -- Digital and Minimally Invasive Biomarkers in Dermatology. |
| Record Nr. | UNINA-9910986145003321 |
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Norman Robert
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| Cham : , : Springer Nature Switzerland : , : Imprint : Springer, , 2025 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Soggetto topico
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Medical Genetics
(110)
- Medical genetics (110)
- Biomedical Research (23)
- Biology - Research (22)
- Medicine - Research (22)