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1Academic Journal
المؤلفون: Divya Pidishetty, Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
المصدر: Stem Cell Research, Vol 78, Iss , Pp 103458- (2024)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
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2Academic Journal
المؤلفون: Sudipta Mahato, Savitri Maddileti, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
المصدر: Stem Cell Research, Vol 77, Iss , Pp 103380- (2024)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
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3Academic Journal
المؤلفون: Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Vivek Pravin Dave, Milind Naik, Mohammad Javed Ali, Chitra Kannabiran, Subhadra Jalali, Giridhara R. Jayandharan, Indumathi Mariappan
المصدر: Stem Cell Research, Vol 77, Iss , Pp 103413- (2024)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
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4Academic Journal
المؤلفون: Divya Pidishetty, Savitri Maddileti, Sudipta Mahato, Trupti Agrawal, Vinay Kumar Pulimamidi, Milind Naik, Chitra Kannabiran, Subhadra Jalali, Indumathi Mariappan
المصدر: Stem Cell Research, Vol 77, Iss , Pp 103418- (2024)
مصطلحات موضوعية: Biology (General), QH301-705.5
وصف الملف: electronic resource
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5Academic Journal
المؤلفون: Neet Mehta, Anshuman Verma, Divya Sree Achanta, Chitra Kannabiran, Sanhita Roy, Dilip Kumar Mishra, Sunita Chaurasia, Deepak Paul Edward, Muralidhar Ramappa
المصدر: Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 405-416 (2023)
مصطلحات موضوعية: congenital hereditary endothelial dystrophy, corneal endothelial dystrophies in childhood, solute carrier family 4 member 11 (slc4a11), Ophthalmology, RE1-994
وصف الملف: electronic resource
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6Academic Journal
المؤلفون: Mohd Salman, Anshuman Verma, Sunita Chaurasia, Deeksha Prasad, Chitra Kannabiran, Vivek Singh, Muralidhar Ramappa
المصدر: Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
مصطلحات موضوعية: CHED, SLC4A11, Corneal dystrophy, Variations, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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7Academic Journal
المصدر: Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2239-2248 (2022)
مصطلحات موضوعية: ched, corneal endothelium, endothelial dystrophy, fecd, genetics, genotype, phenotype, ppcd, Ophthalmology, RE1-994
وصف الملف: electronic resource
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8Academic Journal
المؤلفون: Mohd Salman, Anshuman Verma, Sunita Chaurasia, Deeksha Prasad, Chitra Kannabiran, Vivek Singh, Muralidhar Ramappa
المصدر: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-1 (2023)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1750-1172
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9Academic Journal
المؤلفون: Chitra Kannabiran, Deepika Parameswarappa, Subhadra Jalali
المصدر: Frontiers in Genetics, Vol 13 (2022)
مصطلحات موضوعية: retinitis pigmentosa, retinal dystrophies, genetics, homozygosity, gene mapping, mutations, Genetics, QH426-470
وصف الملف: electronic resource
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10Academic Journal
المؤلفون: Derin M. Thomas, Chitra Kannabiran, D. Balasubramanian
المصدر: Frontiers in Medicine, Vol 8 (2021)
مصطلحات موضوعية: persistent hyperplastic primary vitreous, gene ontology, bioinformatic analysis, hub genes, molecular pathway, Medicine (General), R5-920
وصف الملف: electronic resource
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11Academic Journal
المصدر: Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2550-2551 (2022)
مصطلحات موضوعية: Ophthalmology, RE1-994
وصف الملف: electronic resource
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12Academic Journal
المؤلفون: Swapna S. Shanbhag, Madhuri A. Koduri, Chitra Kannabiran, Pragnya R. Donthineni, Vivek Singh, Sayan Basu
المصدر: Frontiers in Genetics, Vol 11 (2021)
مصطلحات موضوعية: human leucocyte antigen, genetic markers, India, carbamazepine, anti-epileptics, toxic epidermal necrolysis, Genetics, QH426-470
وصف الملف: electronic resource
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13Academic Journal
المصدر: Indian Journal of Ophthalmology, Vol 59, Iss 5, Pp 398-400 (2011)
مصطلحات موضوعية: Pediatric traumatic cataract, primary posterior capsulotomy, posterior capsule opacification, square-edge intraocular lens, visual axis opacification, Multifocal electroretinogram, principal components′, analysis, retinitis pigmentosa, Behcet′s disease, HLA-B51, optical coherence tomography, macular hole, Graves′ ophthalmopathy, thyroid eye disease, unilateral, Assam, corneal ulcer, fusarium, mycotic keratitis, Antifungal sensitivity testing, amphotericin B, Aspergillus, fungal keratitis, polymerase chain reaction--single-stranded conformational polymorphism., Lid coloboma, limbal dermoid, nasopalpebral lipoma-coloboma syndrome, Bilateral, breast metastasis, extraocular muscle, Conventional dacryocystorhinostomy, trans-canalicular laser-assisted dacryocystorhinostomy, Eye surgery, operation theater, parental presence, squint surgery, witnessing a surgery, Centrocecal visual field defect, cilioretinal artery occlusion, fluorescein angiogram, intranasal cocaine, Caesarean section, epidural anesthesia, Horner′s syndrome, Acute myeloid leukemia, hypopyon, masquerade syndrome, Low-fluence photodynamic therapy, choroidal neovascular membrane, choroidal osteoma, ranibizumab, Cataract surgery, perfluorocarbon liquid, postoperative inflammation, Bilateral keratoconus, granular dystrophy, late occurrence, Ophthalmology, RE1-994
وصف الملف: electronic resource
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14
المؤلفون: Sunita Chaurasia, Shalini Singh, Sujata Das, Saumya Jakati, Chitra Kannabiran
المصدر: Current Eye Research. 46:765-770
مصطلحات موضوعية: Macular corneal dystrophy, medicine.medical_specialty, Visual acuity, genetic structures, Vision Disorders, Visual Acuity, Corneal dystrophy, Cornea, Glycosaminoglycan, Cellular and Molecular Neuroscience, Stroma, Ophthalmology, medicine, Humans, Corneal Dystrophies, Hereditary, business.industry, medicine.disease, eye diseases, Sensory Systems, Corneal transparency, Mutation, Histopathology, Full thickness, sense organs, Sulfotransferases, medicine.symptom, business
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15
المؤلفون: Chitra Kannabiran
المصدر: Mapping Scientific Method ISBN: 9781003298908
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16
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17
المؤلفون: Chitra Kannabiran
المصدر: Ophthalmic genetics. 41(6)
مصطلحات موضوعية: 0301 basic medicine, 030105 genetics & heredity, Biology, Cell biology, DNA-Binding Proteins, 03 medical and health sciences, Ophthalmology, 0302 clinical medicine, Pediatrics, Perinatology and Child Health, Mutation, Retinal Dystrophies, 030221 ophthalmology & optometry, Humans, Spermatogenesis, Gene, Genetics (clinical)
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18Academic Journal
المؤلفون: J Med, Balasubramanya Genet, Chitra Ramamurthy, Surya Kannabiran, G Prakash, Kekunnaya Ponnam, Sushma Ramesha, Tejwani, Surya Prakash, G Ponnam, Kekunnaya Ramesha, Sushma Tejwani, Chitra Kannabiran . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.1061.2855; http://www.tezu.ernet.in/dmbbt/people/SPG/gap.pdf
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19
المؤلفون: Chitra Kannabiran, Indumathi Mariappan
المصدر: Journal of Genetics. 97:341-352
مصطلحات موضوعية: 0301 basic medicine, Retinal Disorder, Genetic enhancement, Disease, Biology, Bioinformatics, Retinoids, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Neurotrophic factors, Genetics, Animals, Humans, Nerve Growth Factors, Clinical Trials as Topic, Genetic heterogeneity, Retinal Degeneration, Retinal, Genetic Therapy, Visual Prosthesis, 030104 developmental biology, chemistry, Visual prosthesis, 030221 ophthalmology & optometry, Eye disorder
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20
المصدر: Cornea. 39(3)
مصطلحات موضوعية: Proband, Adult, Male, Heterozygote, Adolescent, Genotype, Nonsense mutation, Anion Transport Proteins, DNA Mutational Analysis, India, Comorbidity, medicine.disease_cause, Genetic analysis, Antiporters, Loss of heterozygosity, 03 medical and health sciences, 0302 clinical medicine, medicine, Missense mutation, Humans, Child, Genetics, Corneal Dystrophies, Hereditary, Mutation, business.industry, Fuchs' Endothelial Dystrophy, Homozygote, DNA, Middle Aged, medicine.disease, Ophthalmology, Child, Preschool, 030221 ophthalmology & optometry, Female, Congenital hereditary endothelial dystrophy, business, 030217 neurology & neurosurgery