-
1دورية أكاديمية
المؤلفون: Yang, Shao H, Procaccia, Shiri, Jung, Hea-Jin, Nobumori, Chika, Tatar, Angelica, Tu, Yiping, Bayguinov, Yulia R, Hwang, Sung Jin, Tran, Deanna, Ward, Sean M, Fong, Loren G, Young, Stephen G
المصدر: Human molecular genetics. 24(10)
مصطلحات موضوعية: Neurons, Enteric Nervous System, Animals, Mice, Transgenic, Mice, Esophageal Achalasia, Lamin Type A, MicroRNAs, RNA Interference, Mutation, Female, Male, Protein Prenylation, Gene Knock-In Techniques, Genetics, Digestive Diseases, Neurosciences, Rare Diseases, Aetiology, 2.1 Biological and endogenous factors, Neurological, Biological Sciences, Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/0nw197mcTest
-
2
المؤلفون: Shao H. Yang, Douglas A. Andres, Yibin Wang, Stephen G. Young, Loren G. Fong, H. Peter Spielmann, Shuxun Ren, Sandy Y. Chang
المصدر: Human Molecular Genetics. 20:436-444
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Protein Prenylation, Biology, Mice, Progeria, Prenylation, Gene knockin, Genetics, medicine, Animals, Farnesyltranstransferase, Gene Knock-In Techniques, Enzyme Inhibitors, Protein Precursors, Allele, Nuclear protein, Molecular Biology, Genetics (clinical), integumentary system, Farnesyltransferase inhibitor, Imidazoles, Nuclear Proteins, Articles, General Medicine, Lamin Type A, Progerin, medicine.disease, Molecular biology, Phenotype, Amino Acid Substitution, Mutation, Cancer research, Protein prenylation, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::884fedf31d7f8a145a658c5b17c90dc4Test
https://doi.org/10.1093/hmg/ddq490Test -
3
المؤلفون: Yulia Bayguinov, Sean M. Ward, Angelica Tatar, Yiping Tu, Sung Jin Hwang, Chika Nobumori, Shiri Procaccia, Hea-Jin Jung, Loren G. Fong, Shao H. Yang, Deanna Tran, Stephen G. Young
المصدر: Human molecular genetics, vol 24, iss 10
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Transgene, Protein Prenylation, Mice, Transgenic, Neuropathology, Biology, Medical and Health Sciences, Transgenic, Enteric Nervous System, LMNA, Mice, Rare Diseases, medicine, Genetics, 2.1 Biological and endogenous factors, Animals, Gene Knock-In Techniques, Aetiology, Molecular Biology, Genetics (clinical), Genetics & Heredity, Neurons, Progeria, integumentary system, Neurosciences, nutritional and metabolic diseases, General Medicine, Articles, Biological Sciences, medicine.disease, Progerin, Lamin Type A, Cell biology, Esophageal Achalasia, MicroRNAs, Neurological, Mutation, Protein prenylation, Enteric nervous system, Female, RNA Interference, Digestive Diseases, Lamin
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d7fe50e2e8d35751d29838fbc78b33Test
https://pubmed.ncbi.nlm.nih.gov/25652409Test -
4
المؤلفون: Kollu N. Rao, Hemant Khanna, Manisha Anand, Wei Zhang, Linjing Li
المصدر: Human Molecular Genetics. :ddw281
مصطلحات موضوعية: Male, 0301 basic medicine, Protein Prenylation, Biology, Ciliopathies, Retina, Joubert syndrome, Cell Line, Mice, 03 medical and health sciences, 0302 clinical medicine, Bardet–Biedl syndrome, Cerebellum, INPP5E, Genetics, medicine, Animals, Humans, Abnormalities, Multiple, Protein Interaction Domains and Motifs, Cilia, Eye Abnormalities, Eye Proteins, Molecular Biology, Genetics (clinical), Cyclic Nucleotide Phosphodiesterases, Type 6, Cilium, Articles, General Medicine, Retinitis pigmentosa GTPase regulator, Kidney Diseases, Cystic, medicine.disease, Phosphoric Monoester Hydrolases, eye diseases, Cell biology, Protein Transport, Ciliopathy, 030104 developmental biology, 030221 ophthalmology & optometry, Protein prenylation, Carrier Proteins, Retinitis Pigmentosa
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e26a9dd864eb624d64d45ee37fa3ee2Test
https://doi.org/10.1093/hmg/ddw281Test -
5
المؤلفون: Richard H. Barnes, Stephen G. Young, Jan Lammerding, Yibin Wang, H. Peter Spielmann, Shuxun Ren, Loren G. Fong, Douglas A. Andres, Yiping Tu, Brandon S.J. Davies
المصدر: Human molecular genetics. 19(13)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Protein Prenylation, Mice, Inbred Strains, Biology, LMNA, Mice, Progeria, Genetics, medicine, Animals, Gene Knock-In Techniques, Nuclear protein, Protein Precursors, Molecular Biology, Genetics (clinical), chemistry.chemical_classification, Nucleoplasm, integumentary system, nutritional and metabolic diseases, Nuclear Proteins, General Medicine, Articles, Fibroblasts, medicine.disease, Lamin Type A, Amino acid, Cell biology, chemistry, Biochemistry, Models, Animal, Protein prenylation, Restrictive dermopathy, Cardiomyopathies, Lamin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09b11df9278330e56109b024a9535f4Test
https://pubmed.ncbi.nlm.nih.gov/20421363Test -
6
المؤلفون: Brandon S.J. Davies, William E. Lowry, Yiping Tu, Andrew C. White, Hung Trinh, Sandy Y. Chang, Martin O. Bergo, Roger Lee, Loren G. Fong, Stephen G. Young
المصدر: Human molecular genetics. 19(8)
مصطلحات موضوعية: Keratinocytes, Male, Farnesyltransferase, Transgene, Protein Prenylation, Biology, 03 medical and health sciences, Mice, 0302 clinical medicine, Keratin, Conditional gene knockout, Genetics, medicine, Animals, Farnesyltranstransferase, Molecular Biology, Genetics (clinical), Cells, Cultured, 030304 developmental biology, Skin, chemistry.chemical_classification, Mice, Knockout, 0303 health sciences, Alkyl and Aryl Transferases, integumentary system, General Medicine, Articles, Molecular biology, 3. Good health, medicine.anatomical_structure, chemistry, Knockout mouse, biology.protein, Protein geranylgeranyltransferase type I, Protein prenylation, Female, Keratinocyte, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c4e3fa8387aee37f0e4f554f268e5cTest
https://pubmed.ncbi.nlm.nih.gov/20106865Test