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1دورية أكاديمية
المؤلفون: Yang, Li, Slone, Jesse, Li, Zhuo, Lou, Xiaoting, Hu, Yueh-Chiang, Queme, Luis F, Jankowski, Michael P, Huang, Taosheng
المصدر: Human molecular genetics. 29(4)
مصطلحات موضوعية: Animals, Mice, Inbred C57BL, Mice, Inbred DBA, Mice, Knockout, Mice, Dependovirus, Central Nervous System Diseases, Ataxia, Mitochondrial Diseases, Disease Models, Animal, Phosphate Transport Proteins, Genetic Vectors, Female, Male, Genetic Therapy, Neurosciences, Rare Diseases, Gene Therapy, Genetics, Neurodegenerative, Biotechnology, Development of treatments and therapeutic interventions, 5.2 Cellular and gene therapies, Neurological, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/52m9n38hTest
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2دورية أكاديمية
المؤلفون: Li, Zhuo, Peng, Yanyan, Hufnagel, Robert B, Hu, Yueh-Chiang, Zhao, Chuntao, Queme, Luis F, Khuchua, Zaza, Driver, Ashley M, Dong, Fei, Lu, Q Richard, Lindquist, Diana M, Jankowski, Michael P, Stottmann, Rolf W, Kao, Winston WY, Huang, Taosheng
المصدر: Human molecular genetics. 26(19)
مصطلحات موضوعية: Retinal Ganglion Cells, Mitochondria, Animals, Mice, Knockout, Humans, Mice, Ataxia, Phosphate Transport Proteins, Mitochondrial Proteins, Mutation, Female, Male, Mitochondrial Dynamics, Neurodegenerative, Pain Research, Eye Disease and Disorders of Vision, Chronic Pain, Neurosciences, Peripheral Neuropathy, Rare Diseases, 2.1 Biological and endogenous factors, Aetiology, Neurological, Eye, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/1d29m7v9Test
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3
المؤلفون: Yanyan Peng, Michael P. Jankowski, Q. Richard Lu, Ashley M. Driver, Winston W.-Y. Kao, Chuntao Zhao, Zaza Khuchua, Zhuo Li, Fei Dong, Luis F. Queme, Taosheng Huang, Diana M. Lindquist, Robert B. Hufnagel, Rolf W. Stottmann, Yueh-Chiang Hu
المصدر: Human Molecular Genetics. 26:3776-3791
مصطلحات موضوعية: Male, Retinal Ganglion Cells, 0301 basic medicine, Cerebellum, Ataxia, Biology, Mitochondrion, Mitochondrial Dynamics, Retinal ganglion, Mitochondrial Proteins, Mice, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Animals, Humans, Phosphate Transport Proteins, Axon, Molecular Biology, Genetics (clinical), Mice, Knockout, Neurodegeneration, Articles, General Medicine, Anatomy, medicine.disease, Mitochondria, Cell biology, Tissue Degeneration, 030104 developmental biology, medicine.anatomical_structure, Mutation, Female, Mitochondrial fission, medicine.symptom, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0990cd47957707760a3ac5489fb8cfTest
https://doi.org/10.1093/hmg/ddx262Test -
4
المؤلفون: Yulia Vistoropsky, Ida Malkin, Gregory Livshits, Svetlana Trofimov, Michal Keter, Eugene Kobyliansky
المصدر: Human Molecular Genetics. 16:1233-1240
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Osteocalcin, Parathyroid hormone, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Russia, Bone remodeling, Cohort Studies, Mice, Internal medicine, Ethnicity, Genetics, medicine, Animals, Homeostasis, Humans, Phosphate Transport Proteins, SNP, Molecular Biology, Genetics (clinical), Calcium metabolism, Haplotype, General Medicine, Middle Aged, Endocrinology, Parathyroid Hormone, Calcium ion homeostasis, biology.protein, Calcium, Female, Bone Remodeling
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf35eab72374931d341ba5059649424bTest
https://doi.org/10.1093/hmg/ddm071Test -
5
المؤلفون: Xi Jiang, Hector L. Aguila, Liping Wang, Ernst J Reichenberger, I-Ping Chen
المصدر: Human molecular genetics. 20(5)
مصطلحات موضوعية: Male, medicine.medical_specialty, Hyperostosis, Facial Paralysis, Osteoclasts, Biology, Pyrophosphate, Exon, chemistry.chemical_compound, Mice, Calcification, Physiologic, Craniomandibular Disorders, Osteogenesis, Internal medicine, Genetics, medicine, Extracellular, Animals, Humans, Phosphate Transport Proteins, Molecular Biology, Genetics (clinical), Cells, Cultured, Sequence Deletion, Bone Diseases, Developmental, Osteoblasts, PHEX, Skull, Gene Expression Regulation, Developmental, Membrane Proteins, Osteoblast, Cell Differentiation, General Medicine, Exons, Articles, medicine.disease, Phenotype, Mice, Inbred C57BL, Disease Models, Animal, Fibroblast Growth Factor-23, medicine.anatomical_structure, Endocrinology, chemistry, Case-Control Studies, Mutation, Osteoporosis, Female, Homeostasis
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ec69d77931d7aebb98f951c45cdcc2fTest
https://pubmed.ncbi.nlm.nih.gov/21149338Test