Restoration of normal BMP signaling levels and osteogenic differentiation in FOP mesenchymal progenitor cells by mutant allele-specific targeting von Kaplan, J, Kaplan, F S, Shore, E M

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GNAS-associated disorders of cutaneous ossification: Two different clinical presentations von Schimmel, R.J, Pasmans, S.G.M.A, Xu, M, Stadhouders-Keet, S.A.E, Shore, E.M, Kaplan, F.S, Wulffraat, N.M

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Overexpression of an Osteogenic Morphogen in Fibrodysplasia Ossificans Progressiva von Shafritz, Adam B, Shore, Eileen M, Gannon, Francis H, Zasloff, Michael A, Taub, Rebecca, Muenke, Maximilian, Kaplan, Frederick S

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Biosynthesis of the cell adhesion molecule uvomorulin (E-cadherin) in Madin-Darby canine kidney epithelial cells von SHORE, E. M, NELSON, W. J

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Identification of a Membrane-Cytoskeletal Complex Containing the Cell Adhesion Molecule Uvomorulin (E-Cadherin), Ankyrin, and Fodrin in Madin-Darby Canine Kidney Epithelial Cells von Nelson, W. James, Shore, Eileen M., Wang, Allan Z., Hammerton, Rachel W.

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Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP) von Xu, M-Q, Feldman1, G, Le Merrer, M, Shugart, YY, Glaser, DL, Urtizberea, JA, Fardeau, M, Connor, JM, Triffitt, J, Smith, R, Shore, EM, Kaplan, FS

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Paternally Inherited Inactivating Mutations of the GNAS1 Gene in Progressive Osseous Heteroplasia von Shore, Eileen M, Ahn, Jaimo, de Beur, Suzanne Jan, Li, Ming, Xu, Meiqi, Gardner, R.J. McKinlay, Zasloff, Michael A, Whyte, Michael P, Levine, Michael A, Kaplan, Frederick S

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Progressive Osseous Heteroplasia von Kaplan, Frederick S., Shore, Eileen M.

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Encrypted morphogens of skeletogenesis: Biological errors and pharmacologic potentials von Kaplan, Frederick S., Shore, Eileen M.

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Deficiency of the α‐Subunit of the Stimulatory G Protein and Severe Extraskeletal Ossification von Eddy, Mark C., Jan de beur, Suzanne M., Yandow, Suzanne M., McAlister, William H., Shore, Eileen M., Kaplan, Frederick S., Whyte, Michael P., Levine, Michael A.

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Bone morphogenetic proteins and c-fos: Early signals in endochondral bone formation von Kaplan, F.S., Shore, E.M.

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Phenotypic and molecular heterogeneity in fibrodysplasia ossificans progressiva von Virdi, A S, Shore, E M, Oreffo, R O, Li, M, Connor, J M, Smith, R, Kaplan, F S, Triffitt, J T

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Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement von Mantovani, Giovanna, Bastepe, Murat, Monk, David, de Sanctis, Luisa, Thiele, Susanne, Usardi, Alessia, Ahmed, S. Faisal, Bufo, Roberto, Choplin, Timothée, De Filippo, Gianpaolo, Devernois, Guillemette, Eggermann, Thomas, Elli, Francesca M., Freson, Kathleen, García Ramirez, Aurora, Germain-Lee, Emily L., Groussin, Lionel, Hamdy, Neveen, Hanna, Patrick, Hiort, Olaf, Jüppner, Harald, Kamenický, Peter, Knight, Nina, Kottler, Marie-Laure, Le Norcy, Elvire, Lecumberri, Beatriz, Levine, Michael A., Mäkitie, Outi, Martin, Regina, Martos-Moreno, Gabriel Ángel, Minagawa, Masanori, Murray, Philip, Pereda, Arrate, Pignolo, Robert, Rejnmark, Lars, Rodado, Rebecca, Rothenbuhler, Anya, Saraff, Vrinda, Shoemaker, Ashley H., Shore, Eileen M., Silve, Caroline, Turan, Serap, Woods, Philip, Zillikens, M. Carola, Perez de Nanclares, Guiomar, Linglart, Agnès

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Heterozygous inactivation of Gnas in adipose‐derived mesenchymal progenitor cells enhances osteoblast differentiation and promotes heterotopic ossification von Pignolo, Robert J, Xu, Meiqi, Russell, Elizabeth, Richardson, Alec, Kaplan, Josef, Billings, Paul C, Kaplan, Frederick S, Shore, Eileen M

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Fibrodysplasia ossificans progressiva von MAHBOUBI, Soroosh, GLASER, David L, SHORE, Eileen M, KAPLAN, Frederick S

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GNAS1 Mutation and Cbfa1 Misexpression in a Child with Severe Congenital Platelike Osteoma Cutis von Yeh, George L., Mathur, Sameer, Wivel, Ashley, Li, Ming, Gannon, Francis H., Ulied, Angels, Audi, Laura, Olmsted, Elizabeth A., Kaplan, Frederick S., Shore, Eileen M.

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Osteoinductive signals and heterotopic ossification von Shore, Eileen M

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A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva von LeMerrer, Martine, Zasloff, Michael, Morhart, Rolf, Kaplan, Frederick S, Cho, Tae-Joon, Choi, In Ho, Glaser, David L, Connor, J Michael, Smith, Roger, Triffitt, James T, Shore, Eileen M, Urtizberea, J Andoni, Feldman, George J, Xu, Meiqi, Delai, Patricia, Rogers, John G, Fenstermacher, David A, Brown, Matthew A

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Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients von Mantovani, Giovanna, Bastepe, Murat, Monk, David, de Sanctis, Luisa, Thiele, Susanne, Ahmed, S. Faisal, Bufo, Roberto, Choplin, Timothée, De Filippo, Gianpaolo, Devernois, Guillemette, Eggermann, Thomas, Elli, Francesca M., Garcia Ramirez, Aurora, Germain-Lee, Emily L., Groussin, Lionel, Hamdy, Neveen A.T., Hanna, Patrick, Hiort, Olaf, Jüppner, Harald, Kamenický, Peter, Knight, Nina, Le Norcy, Elvire, Lecumberri, Beatriz, Levine, Michael A., Mäkitie, Outi, Martin, Regina, Martos-Moreno, Gabriel Ángel, Minagawa, Manasori, Murray, Philip, Pereda, Arrate, Pignolo, Robert, Rejnmark, Lars, Rodado, Rebeca, Rothenbuhler, Anya, Saraff, Vrinda, Shoemaker, Ashley H., Shore, Eileen M., Silve, Caroline, Turan, Serap, Woods, Philip, Zillikens, M. Carola, Perez de Nanclares, Guiomar, Linglart, Agnès

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Dysregulation of the BMP‐p38 MAPK Signaling Pathway in Cells From Patients With Fibrodysplasia Ossificans Progressiva (FOP) von Fiori, Jennifer L, Billings, Paul C, de la Peña, Lourdes Serrano, Kaplan, Frederick S, Shore, Eileen M

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