نتائج البحث - Michael Pope

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  1. 1
    Connective Tissue Disease: Molecular Pathology of the Extracellular Matrix

    Connective Tissue Disease: Molecular Pathology of the Extracellular Matrix حسب F. Michael Pope

    منشور في 1987
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  2. 2
    Autosomal Dominant Cutis Laxa with Severe Lung Disease: Synthesis and Matrix Deposition of Mutant Tropoelastin

    Autosomal Dominant Cutis Laxa with Severe Lung Disease: Synthesis and Matrix Deposition of Mutant Tropoelastin حسب Zsolt Urbán, Jimin Gao, F. Michael Pope, Elaine C. Davis

    منشور في 2005
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  3. 3
    Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndrome.

    Abnormalities of the lungs and thoracic cage in the Ehlers-Danlos syndrome. حسب Jon G. Ayres, F. Michael Pope, John Reidy, T. J. Clark

    منشور في 1985
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  4. 4
    The gene responsible for Werner syndrome may be a cell division "counting" gene.

    The gene responsible for Werner syndrome may be a cell division "counting" gene. حسب Richard Faragher, Ian R. Kill, J A Hunter, F. Michael Pope, Charles Tannock, Sydney Shall

    منشور في 1993
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  5. 5
    Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity

    Stickler syndrome: further mutations in COL11A1 and evidence for additional locus heterogeneity حسب Sam Martin, Allan J. Richards, John R.W. Yates, John D. Scott, Michael Pope, Martin P. Snead

    منشور في 1999
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  6. 6
    The Ehlers–Danlos syndromes, rare types

    The Ehlers–Danlos syndromes, rare types حسب Angela F. Brady, Serwet Demirdas, Sylvie Fournel‐Gigleux, Neeti Ghali, Cecilia Giunta, Ines Kapferer‐Seebacher, Tomoki Kosho, Roberto Mendoza‐Londono, Michael Pope, Marianne Rohrbach, Tim Van Damme, Anthony Vandersteen, Caroline van Mourik, Nicol C. Voermans, Johannes Zschocke, Fransiska Malfait

    منشور في 2017
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    Revisão
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  7. 7
    The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21

    The Gene for Juvenile Hyaline Fibromatosis Maps to Chromosome 4q21 حسب Nazneen Rahman, Melanie Dunstan, M. Dawn Teare, Sandra Hanks, Sarah Edkins, Jaime Hughes, Graham R. Bignell, Grazia M.S. Mancini, Wim J. Kleijer, Mary Ellen Campbell, Gökhan Keser, Carol M. Black, Nigel Williams, Laura Arbour, Matthew L. Warman, Andrea Superti‐Furga, P. Andrew Futreal, F. Michael Pope

    منشور في 2002
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  8. 8
    Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature

    Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature حسب Bert Callewaert, Bart Loeys, Anna Ficcadenti, Sascha Vermeer, Magnus Landgren, Hester Y. Kroes, Yuval Yaron, Michael Pope, Nicola Foulds, Odile Boute, Francisco Galán, Helen Kingston, Nathalie Van der Aa, Iratxe Salcedo, Mariëlle E.M. Swinkels, Carina Wallgren‐Pettersson, Orazio Gabrielli, Julie De Backer, Paul Coucke, Anne M. De Paepe

    منشور في 2008
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  9. 9
    Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis

    Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis حسب Sandra Hanks, Sarah Adams, Jenny Douglas, Laura Arbour, David J. Atherton, Sevim Balcı, Harald Bode, Mary Ellen Campbell, Murray Feingold, Gökhan Keser, Wim J. Kleijer, Grazia M.S. Mancini, John A. McGrath, Francesco Muntoni, Arti Nanda, M. Dawn Teare, Matthew L. Warman, F. Michael Pope, Andrea Superti‐Furga, P. Andrew Futreal, Nazneen Rahman

    منشور في 2003
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  10. 10
    Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A

    Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A حسب Eyal Reinstein, Sophia Frentz, Tim Morgan, Sixto García‐Miñaúr, Richard J. Leventer, George McGillivray, Mitchel Pariani, Anthony van der Steen, Michael Pope, Muriel Holder‐Espinasse, Richard H. Scott, Elizabeth M. Thompson, Terry Robertson, Brian Coppin, Robert J. Siegel, Montserrat Bret Zurita, José Ignacio Rodrı́guez, Carmen del Rocío Monedero Morales, Yuri Blanc Rodrigues, Joaquín Arcas, Anand Saggar, Margaret A. Horton, Elaine H. Zackai, John M. Graham, David L. Rimoin, Stephen P. Robertson

    منشور في 2012
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  11. 11
    The 2017 international classification of the Ehlers–Danlos syndromes

    The 2017 international classification of the Ehlers–Danlos syndromes حسب Fransiska Malfait, Clair A. Francomano, Peter H. Byers, John W. Belmont, Britta Berglund, James H. Black, Lara Bloom, Jessica Bowen, Angela F. Brady, Nigel Burrows, Marco Castori, Helen Cohen, Marina Colombi, Serwet Demirdas, Julie De Backer, Anne De Paepe, Sylvie Fournel‐Gigleux, Michael Frank, Neeti Ghali, Cecilia Giunta, Rodney Grahame, Alan J. Hakim, Xavier Jeunemaı̂tre, Diana Johnson, Birgit Juul‐Kristensen, Ines Kapferer‐Seebacher, Hanadi Kazkaz, Tomoki Kosho, Mark E. Lavallee, Howard P. Levy, Roberto Mendoza‐Londono, Melanie Pepin, F. Michael Pope, Eyal Reinstein, Leema Robert, Marianne Rohrbach, Lynn Sanders, Glenda Sobey, Tim Van Damme, Anthony Vandersteen, Caroline van Mourik, Nicol Voermans, Nigel Wheeldon, Johannes Zschocke, Brad T. Tinkle

    منشور في 2017
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