Mutations of the GNAS1 Gene, Stromal Cell Dysfunction, and Osteomalacic Changes in Non–McCune–Albright Fibrous Dysplasia of Bone
Bianco, P., Riminucci, M., Majolagbe, A., Kuznetsov, S. A., Collins, M. T., Mankani, M. H., Corsi, A., Bone, H. G., Wientroub, S., Spiegel, A. M., Fisher, L. W., Gehron ROBEY, P.
Published in Journal of bone and mineral research (01.01.2000)
Published in Journal of bone and mineral research (01.01.2000)
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Fibrous dysplasia of bone in the McCune-Albright syndrome: abnormalities in bone formation
Riminucci, M, Fisher, LW, Shenker, A, Spiegel, AM, Bianco, P, Gehron Robey, P
Published in The American journal of pathology (01.12.1997)
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Published in The American journal of pathology (01.12.1997)
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Stable overexpression of MEN1 suppresses tumorigenicity of RAS
KIM, Y. S, BURNS, A. L, GOLDSMITH, P. K, HEPPNER, C, PARK, S. Y, CHANDRASEKHARAPPA, S. C, COLLINS, F. S, SPIEGEL, A. M, MARX, S. J
Published in Oncogene (21.10.1999)
Published in Oncogene (21.10.1999)
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Multiple endocrine neoplasia type 1: clinical and genetic topics
Marx, S, Spiegel, A M, Skarulis, M C, Doppman, J L, Collins, F S, Liotta, L A
Published in Annals of internal medicine (15.09.1998)
Published in Annals of internal medicine (15.09.1998)
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The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gsα gene: site-specific patterns and recurrent histological hallmarks
Riminucci, Mara, Liu, Bin, Corsi, Alessandro, Shenker, Andrew, Spiegel, Allen M., Robey, Pamela Gehron, Bianco, Paolo
Published in The Journal of pathology (01.01.1999)
Published in The Journal of pathology (01.01.1999)
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Menin molecular interactions: insights into normal functions and tumorigenesis
Agarwal, S K, Kennedy, P A, Scacheri, P C, Novotny, E A, Hickman, A B, Cerrato, A, Rice, T S, Moore, J B, Rao, S, Ji, Y, Mateo, C, Libutti, S K, Oliver, B, Chandrasekharappa, S C, Burns, A L, Collins, F S, Spiegel, A M, Marx, S J
Published in Hormone and metabolic research (01.06.2005)
Published in Hormone and metabolic research (01.06.2005)
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The G protein coupled to the thromboxane A2 receptor in human platelets is a member of the novel Gq family
SHENKER, A, GOLDSMITH, P, UNSON, C. G, SPIEGEL, A. M
Published in The Journal of biological chemistry (15.05.1991)
Published in The Journal of biological chemistry (15.05.1991)
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Mutations of the Gsα-Subunit Gene in Albright Hereditary Osteodystrophy Detected by Denaturing Gradient Gel Electrophoresis
Weinstein, Lee S., Gejman, Pablo V., Friedman, Eitan, Kadowaki, Takashi, Collins, Regina M., Gershon, Elliot S., Spiegel, Allen M.
Published in Proceedings of the National Academy of Sciences - PNAS (01.11.1990)
Published in Proceedings of the National Academy of Sciences - PNAS (01.11.1990)
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MEN1 gene analysis in sporadic adrenocortical neoplasms
HEPPNER, C, REINCKE, M, AGARWAL, S. K, MORA, P, ALLOLIO, B, BURNS, A. L, SPIEGEL, A. M, MARX, S. J
Published in The journal of clinical endocrinology and metabolism (1999)
Published in The journal of clinical endocrinology and metabolism (1999)
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Inborn errors of signal transduction: Mutations in G proteins and G protein‐coupled receptors as a cause of disease
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