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المؤلفون: Mohamed G. Hassan, Christopher Chen, Hanan A. Ismail, Abbas R. Zaher, Timothy C. Cox, Alice F. Goodwin, Andrew H. Jheon
المصدر: Am J Orthod Dentofacial Orthop
مصطلحات موضوعية: Male, Mice, Pregnancy, Dietary Supplements, Animals, Humans, Lactation, Calcium, Female, Phosphorus, Orthodontics, X-Ray Microtomography, Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e23b56773f589aad88d5c87e79131a3eTest
https://doi.org/10.1016/j.ajodo.2021.12.015Test -
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المؤلفون: Andrew H. Jheon, Kenneth M. Huttner, Maya Landan, Ophir D. Klein, Jacob Hogue, Alice F. Goodwin, Wenli Yu, Ramsey Johnson, Dong-Kha Tran, Mary Fete, Tarek Hussein, Miquella G. Chavez, Kyle B. Jones, Kerstin Seidel
المصدر: American journal of medical genetics. Part A, vol 161A, iss 7
مصطلحات موضوعية: Male, Pathology, Ectodermal dysplasia, terminal hair, Terminal hair, SWEAT, pilocarpine iontophoresis, Surveys and Questionnaires, Child, Genetics (clinical), ectodysplasin, Pediatric, Microscopy, Microscopy, Confocal, integumentary system, Pilocarpine, Anatomy, Ectodysplasins, Iontophoresis, Phenotype, medicine.anatomical_structure, Anhidrotic, Confocal, Ectodermal Dysplasia 1, medicine.drug, Adult, medicine.medical_specialty, Adolescent, Clinical Sciences, Dermatology, Biology, confocal imaging, sweat gland, Article, Young Adult, phototrichogram, Sweat gland, Genetics, medicine, X-linked hypohidrotic ectodermal dysplasia, Humans, Hypohidrotic ectodermal dysplasia, Ectodermal Dysplasia 1, Anhidrotic, Reproducibility of Results, hair, medicine.disease, Sweat Glands, Case-Control Studies, Congenital Structural Anomalies, Hair
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0969bba469146c916b9f8901945bbed8Test
https://doi.org/10.1002/ajmg.a.35959Test -
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المؤلفون: Lauren A. Weiss, Katherine A. Rauen, Erika Yeh, Gemma E. Rooney, Jeroen P. Roose, Ophir D. Klein, Erik M. Ullian, Claude M. Schofield, Philippe Depeille, Amnon Sharir, Alice F. Goodwin
المصدر: The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 36, iss 1
مصطلحات موضوعية: 0301 basic medicine, Male, Autism, Cellular differentiation, Regenerative Medicine, Medical and Health Sciences, Costello syndrome, Neural Stem Cells, Stem Cell Research - Nonembryonic - Human, 2.1 Biological and endogenous factors, Aetiology, Induced pluripotent stem cell, Child, Cells, Cultured, Pediatric, Cultured, Stem Cell Research - Induced Pluripotent Stem Cell - Human, General Neuroscience, Costello Syndrome, Cell Differentiation, Articles, Middle Aged, Neural stem cell, Up-Regulation, iPS cells, Mental Health, Child, Preschool, Neurological, Stem Cell Research - Nonembryonic - Non-Human, Female, Stem cell, Adult, Neurite, Adolescent, Cells, Intellectual and Developmental Disabilities (IDD), Induced Pluripotent Stem Cells, Biology, 03 medical and health sciences, Directed differentiation, stem cells, medicine, Humans, cortical development, Preschool, Neurology & Neurosurgery, Stem Cell Research - Induced Pluripotent Stem Cell, Psychology and Cognitive Sciences, Neurosciences, Infant, Stem Cell Research, medicine.disease, Brain Disorders, Developmental disorder, 030104 developmental biology, ras Proteins, Neuroscience, Ras
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c33826688773ee032bb9b125ac8a7e4Test
https://europepmc.org/articles/PMC4701956Test/ -
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المؤلفون: Cyril Charles, Ophir D. Klein, Maya Landan, Snehlata Oberoi, Katherine A. Rauen, Cecilia Fairley, Alice F. Goodwin, Jessica C. Massie
المصدر: American journal of medical genetics. Part A, vol 164A, iss 6
مصطلحات موضوعية: Male, Ectodermal dysplasia, Pathology, Craniofacial abnormality, gingival hyperplasia, Oral and gastrointestinal, Craniofacial Abnormalities, Congenital, Phosphatidylinositol 3-Kinases, Costello syndrome, Ectodermal Dysplasia, 2.1 Biological and endogenous factors, Aetiology, Child, Genetics (clinical), Heart Defects, Pediatric, Dental Enamel Hypoplasia, Costello Syndrome, enamel, Anatomy, craniofacial development, Female, medicine.symptom, Abnormalities, Mitogen-Activated Protein Kinases, CS, Multiple, signal transduction, Heart Defects, Congenital, Adult, medicine.medical_specialty, Pediatric Research Initiative, Adolescent, MAP Kinase Signaling System, Clinical Sciences, occlusion, Biology, RASopathy, Article, Proto-Oncogene Proteins p21(ras), Young Adult, Rare Diseases, stomatognathic system, medicine, Genetics, Humans, Abnormalities, Multiple, HRAS, Craniofacial, Dental/Oral and Craniofacial Disease, Tooth Abnormalities, Macrocephaly, Facies, tooth development, MAPK pathway, malocclusion, medicine.disease, Failure to Thrive, stomatognathic diseases, Gingival Hyperplasia, Mutation, receptor tyrosine kinase, Congenital Structural Anomalies, Tooth, Malocclusion, Ras
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fd303490107e32d7aa99c0270e9802Test
https://escholarship.org/uc/item/1qs5q956Test -
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المؤلفون: Ophir D. Klein, Cyril Charles, Katherine A. Rauen, Xu Zheng, Amnon Sharir, Andrew H. Jheon, William E. Tidyman, Thomas G.H. Diekwisch, Alice F. Goodwin, James A. Fagin, Martin McMahon, Bernhard Ganss
المصدر: Human molecular genetics, vol 23, iss 3
مصطلحات موضوعية: MAPK/ERK pathway, Male, Medical and Health Sciences, Cohort Studies, Mice, Phosphatidylinositol 3-Kinases, Anti-apoptotic Ras signalling cascade, Ameloblasts, 2.1 Biological and endogenous factors, Scanning, Aetiology, Enzyme Inhibitors, Child, Genetics (clinical), Phosphoinositide-3 Kinase Inhibitors, Pediatric, Genetics & Heredity, Microscopy, Costello Syndrome, Cell Polarity, General Medicine, Articles, Biological Sciences, Cell biology, Mutant Strains, Child, Preschool, Female, Ameloblast, Signal Transduction, Adult, Adolescent, 1.1 Normal biological development and functioning, MAP Kinase Kinase Kinase 1, Biology, Electron, Proto-Oncogene Proteins p21(ras), Young Adult, Rare Diseases, stomatognathic system, Underpinning research, Genetics, Animals, Humans, HRAS, Dental/Oral and Craniofacial Disease, Progenitor cell, Preschool, Dental Enamel, Molecular Biology, PI3K/AKT/mTOR pathway, Animal, Infant, Stem Cell Research, Mice, Mutant Strains, Disease Models, Animal, Ras Signaling Pathway, Case-Control Studies, Disease Models, Immunology, Microscopy, Electron, Scanning
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4270d19f5798493b2d515b8ec68baadTest
https://pubmed.ncbi.nlm.nih.gov/24057668Test