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1دورية أكاديمية
المؤلفون: John P Caspersen, Mark C Vanderwel, William G Cole, Drew W Purves
المصدر: PLoS ONE, Vol 6, Iss 12, p e28660 (2011)
وصف الملف: electronic resource
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المؤلفون: Ralph A Zirngibl, Wolfgang Vogel, Luisa Moreno, Tanya Zappitelli, William G. Cole, Janet Rossant, Lucy R. Osborne, Frieda Chen, Jane E. Aubin, Lee Adamson, Esther Rosenthal, Ruolin Guo, Marc D. Grynpas, Ann M. Flenniken, Shousaku Itoh
المصدر: Journal of Bone and Mineral Research. 29:1412-1423
مصطلحات موضوعية: musculoskeletal diseases, Bone mineral, Stromal cell, Chemistry, Endocrinology, Diabetes and Metabolism, Osteoblast, Anatomy, medicine.disease, Molecular biology, Resorption, medicine.anatomical_structure, Osteoclast, Osteogenesis imperfecta, medicine, Orthopedics and Sports Medicine, Bone marrow, Type I collagen
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المؤلفون: Minna Pekkinen, Outi Mäkitie, Terhi J. Heino, Lisette Nevarez, Cynthia J. Curry, Christine M. Laine, Heikki Kröger, Mira Aronen, Kyu Sang Joeng, Maija Wessman, Daniel H. Cohn, Brendan Lee, Deborah Krakow, Philippe M. Campeau, James T. Lu, William G. Cole, Richard A. Gibbs, Monica Grover, Riku Kiviranta, Tero Laine, Vappu Nieminen-Pihala, Kati Tarkkonen, Anna-Elina Lehesjoki
المصدر: New England Journal of Medicine. 368:1809-1816
مصطلحات موضوعية: Adult, Male, animal structures, Adolescent, Nonsense mutation, Genes, Recessive, Mice, Transgenic, 030209 endocrinology & metabolism, Wnt1 Protein, Biology, ta3111, Mice, Young Adult, 03 medical and health sciences, 0302 clinical medicine, PLS3, medicine, Animals, Humans, Missense mutation, Age of Onset, WNT1, Child, Gene, Aged, Genes, Dominant, 030304 developmental biology, Genetics, 0303 health sciences, ta1182, Wnt signaling pathway, General Medicine, Middle Aged, Osteogenesis Imperfecta, medicine.disease, ta3123, Pedigree, medicine.anatomical_structure, Osteogenesis imperfecta, Mutation, Osteoporosis, Female, Bone marrow
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المؤلفون: Marika Löija, Leena Ala-Kokko, Etienne Sochett, Minna Männikkö, Outi Mäkitie, Stefano Mora, William G. Cole, Dirk Schnabel, Johanna Korvala, Harald Jüppner
المصدر: European Journal of Medical Genetics. 55:515-519
مصطلحات موضوعية: Male, Heterozygote, medicine.medical_specialty, Candidate gene, Adolescent, Transcription, Genetic, Osteoporosis, CHO Cells, Biology, Cricetulus, Polymorphism (computer science), Cricetinae, Wnt3A Protein, Internal medicine, AXIN1, Genetics, medicine, Animals, Humans, Genetic Predisposition to Disease, Child, Wnt Signaling Pathway, Genetics (clinical), Polymorphism, Genetic, Case-control study, Heterozygote advantage, LRP5, General Medicine, medicine.disease, Endocrinology, DKK1, Genetic Loci, Case-Control Studies, Intercellular Signaling Peptides and Proteins, Female
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المؤلفون: Jonathan Akikusa, Salvatore Albani, Roger Allen, Khaled Alsaeid, Tadej Avčin, Paul S. Babyn, Arvind Bagga, Karyl S. Barron, Mara L. Becker, Susanne M. Benseler, Timothy Beukelman, Paul Brogan, Hermine I. Brunner, Rubèn Burgos-Vargas, Jill Buyon, David A. Cabral, Sharon Choo, Rolando Cimaz, Robert Allen Colbert, William G. Cole, Iris Davidson, Fabrizio De Benedetti, Andrea S. Doria, Frank Dressler, Ciarán M. Duffy, Despina Eleftheriou, Brian M. Feldman, Polly J. Ferguson, Robert Fuhlbrigge, Marco Gattorno, Alexei A. Grom, Philip J. Hashkes, Kristin Houghton, Hans-Iko Huppertz, Norman T. Ilowite, Edgar Jaeggi, Daniel L. Kastner, Adam Kirton, Marisa Klein-Gitelman, Gay Kuchta, Jerome Charles Lane, Ronald M. Laxer, Claire LeBlanc, Steven J. Leeder, G. Elizabeth Legger, Suzanne C. Li, Carol B. Lindsley, Dan Lovell, Outi Makitie, Alberto Martini, Frederick W. Miller, Kimberly Morishita, Peter A. Nigrovic, Kiem G. Oen, Kathleen M. O'Neil, Seza Ozen, Peri H. Pepmueller, Ross E. Petty, Elena Pope, Sampath Prahalad, Berent Prakken, Michael Rapoff, Lisa G. Rider, Carlos Daniel Rosé, James T. Rosenbaum, Alan M. Rosenberg, Johannes Roth, Ricardo Alberto Guillermo, Rayfel Schneider, Christiaan Scott, David D. Sherry, Earl Silverman, Mary Beth Son, Robert P. Sundel, Susan D. Thompson, Karin Tiedemann, Shirley M.L. Tse, Lori Tucker, Yosef Uziel, Joris van Montfrans, Janitzia Vazques-Mellado, Leanne Ward, Lucy R. Wedderburn, Carine Wouters, James Wright, Nico M. Wulffraat, Lawrence Zemel, Francesco Zulian
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2361a7d29be1e6ac2070f5681103d3ef
https://doi.org/10.1016/b978-0-323-24145-8.00060-0 -
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المؤلفون: William G. Cole, Outi Mäkitie
مصطلحات موضوعية: Pathology, medicine.medical_specialty, medicine.anatomical_structure, business.industry, medicine, Connective tissue, Primary disorders, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::da12d7665cb5bf67974bb1e074b27e6f
https://doi.org/10.1016/b978-0-323-24145-8.00054-5 -
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المؤلفون: Amanda M. Branam, Daniel S. Greenspan, Guorui Huang, Francisco Pelegri, William G. Cole, Richard M. Wenstrup, Guy G. Hoffman
المصدر: Matrix Biology. 29:261-275
مصطلحات موضوعية: Amino Acid Motifs, Protein domain, Article, Animals, Humans, Clade, Molecular Biology, Gene, Zebrafish, Synteny, Genetics, Base Sequence, biology, Alternative splicing, biology.organism_classification, Extracellular Matrix, Protein Structure, Tertiary, Alternative Splicing, Procollagen peptidase, Collagen Type III, Genes, Collagen, Collagen Type V, Procollagen, Function (biology)
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المؤلفون: Heikki Kröger, Outi Mäkitie, William G. Cole, Renata C. Pereira, Tero Laine, Serap Turan, Murat Bastepe, Harald Jüppner, Ilkka Kaitila
المصدر: Journal of Bone and Mineral Research
مصطلحات موضوعية: Fibroblast growth factor 23, Male, medicine.medical_specialty, DMP1, Endocrinology, Diabetes and Metabolism, 030209 endocrinology & metabolism, Genes, Recessive, osteomalacia, skeletal dysplasia, Bone remodeling, 03 medical and health sciences, 0302 clinical medicine, stomatognathic system, Internal medicine, rickets, Medicine, Humans, Orthopedics and Sports Medicine, Bone pain, 030304 developmental biology, Aged, hypophosphatemia, 0303 health sciences, Osteomalacia, FGF-23, Extracellular Matrix Proteins, business.industry, Genetic Carrier Screening, Heterozygote advantage, medicine.disease, Phosphoproteins, Pedigree, Hypophosphatemic Rickets, Fibroblast Growth Factor-23, Endocrinology, Phenotype, Mutation, Original Article, Female, medicine.symptom, business, Hypophosphatemia
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المؤلفون: Daniel D. Carson, Jacqueline T. Hecht, Dina Montufar-Solis, Mark B. Snuggs, Allison Scott, Tiffany Sanford, P. Jackie Duke, Deborah Hogue, William G. Cole, Mark A. Bernard, W. Barry Van Winkle
المصدر: Journal of Bone and Mineral Research. 15:442-450
مصطلحات موضوعية: Pathology, medicine.medical_specialty, Tumor suppressor gene, Macromolecular Substances, Endocrinology, Diabetes and Metabolism, Hereditary multiple exostoses, Blotting, Western, DNA Mutational Analysis, Biology, N-Acetylglucosaminyltransferases, medicine.disease_cause, Chondrocyte, Germline mutation, medicine, Humans, Protein Isoforms, Vimentin, Actinin, Orthopedics and Sports Medicine, Child, Exostoses, Cytoskeleton, Exostosis, Mutation, Microscopy, Confocal, Cartilage, Proteins, medicine.disease, Actins, Cell biology, medicine.anatomical_structure, Microscopy, Fluorescence, Exostoses, Multiple Hereditary
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المؤلفون: William G. Cole, Kong Wah Ng, Thomas Mascara, John F. Bateman, Paul R. Gummer, V. P. Michelangeli, T. John Martin
المصدر: Journal of Bone and Mineral Research. 3:53-61
مصطلحات موضوعية: musculoskeletal diseases, medicine.medical_specialty, Endocrinology, Diabetes and Metabolism, Retinoic acid, Tretinoin, Calvaria, Biology, Bone and Bones, Cell Line, chemistry.chemical_compound, Internal medicine, medicine, Animals, Doubling time, Orthopedics and Sports Medicine, Dactinomycin, Histocytochemistry, Mesenchymal stem cell, Alkaline Phosphatase, Molecular biology, In vitro, Clone Cells, Rats, Kinetics, medicine.anatomical_structure, Endocrinology, Animals, Newborn, Gene Expression Regulation, chemistry, Alkaline phosphatase, Fetal bovine serum, medicine.drug