Search Results - Marcy C. Speer

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  1. 1
    Candidate gene analysis in human neural tube defects

    Candidate gene analysis in human neural tube defects by Abee L. Boyles, Preston Hammock, Marcy C. Speer

    Published 2005
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  2. 2
    Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

    Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. by Michael J. Econs, Paul T. McEnery, Felicia Lennon, Marcy C. Speer

    Published 1997
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  3. 3
    Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

    Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23 by D. Messina, Marcy C. Speer, Margaret A. Pericak‐Vance, Elizabeth M. McNally

    Published 1997
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  4. 4
    Human neural tube defects: Developmental biology, epidemiology, and genetics

    Human neural tube defects: Developmental biology, epidemiology, and genetics by Eric Detrait, Timothy M. George, Heather Etchevers, John R. Gilbert, Michel Vekemans, Marcy C. Speer

    Published 2005
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  5. 5
    A genetic hypothesis for Chiari I malformation with or without syringomyelia

    A genetic hypothesis for Chiari I malformation with or without syringomyelia by Marcy C. Speer, Timothy M. George, David S. Enterline, Amy Franklin, Chantelle M. Wolpert, Thomas H. Milhorat

    Published 2000
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  6. 6
    Further evidence for a maternal genetic effect and a sex‐influenced effect contributing to risk for human neural tube defects

    Further evidence for a maternal genetic effect and a sex‐influenced effect contributing to risk for human neural tube defects by Kristen Deak, Deborah G. Siegel, Timothy M. George, Simon G. Gregory, Allison E. Ashley‐Koch, Marcy C. Speer

    Published 2008
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  7. 7
    Human neural crest cells display molecular and phenotypic hallmarks of stem cells

    Human neural crest cells display molecular and phenotypic hallmarks of stem cells by Sophie Thomas, Marie Thomas, Patrick Wincker, Candice Babarit, Pu‐Ting Xu, Marcy C. Speer, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Heather Etchevers

    Published 2008
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  8. 8
    Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations

    Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations by Christina A. Markunas, R. Shane Tubbs, Roham Moftakhar, Allison E. Ashley‐Koch, Simon G. Gregory, W. Jerry Oakes, Marcy C. Speer, Bermans J. Iskandar

    Published 2012
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  9. 9
    Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics

    Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics by Marcy C. Speer, David S. Enterline, Lorraine Mehltretter, Preston Hammock, Judith Joseph, Margaret Dickerson, Richard G. Ellenbogen, Thomas H. Milhorat, Michael A. Hauser, Timothy M. George

    Published 2003
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  10. 10
    myotilin Mutation Found in Second Pedigree with LGMD1A

    myotilin Mutation Found in Second Pedigree with LGMD1A by Michael A. Hauser, Cecı́lia Conde, Valeria Kowaljow, Guillermo Zeppa, Ana Lía Taratuto, Udana Torian, Jeffery M. Vance, Margaret A. Pericak‐Vance, Marcy C. Speer, Alberto L. Rosa

    Published 2002
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  11. 11
    Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing

    Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing by Abee L. Boyles, William K. Scott, Eden R. Martin, Silke Schmidt, Yi‐Ju Li, Allison E. Ashley‐Koch, Meredyth P. Bass, Michael A. Schmidt, Margaret A. Pericak‐Vance, Marcy C. Speer, Elizabeth R. Hauser

    Published 2005
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  12. 12
    Gene Expression Profiling of Familial and Sporadic Interstitial Pneumonia

    Gene Expression Profiling of Familial and Sporadic Interstitial Pneumonia by Ivana V. Yang, Lauranell H. Burch, Mark P. Steele, Jordan D. Savov, John W. Hollingsworth, Erin McElvania, Katherine Berman, Marcy C. Speer, Thomas A. Sporn, Kevin K. Brown, Marvin I. Schwarz, David A. Schwartz

    Published 2006
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  13. 13
    Allelic and locus heterogeneity in inherited venous malformations

    Allelic and locus heterogeneity in inherited venous malformations by Jennifer T. Calvert, Travis J. Riney, Christopher D. Kontos, H. Eugene, Víctor G. Prieto, Christopher R. Shea, Jonathan Berg, N. C. Nevin, Sheila A. Simpson, Krystyna A. Pasyk, Marcy C. Speer, Kevin G. Peters, Douglas A. Marchuk

    Published 1999
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  14. 14
    Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions

    Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions by Abee L. Boyles, Ashley V. Billups, Kristen Deak, Deborah G. Siegel, Lorraine Mehltretter, Susan H. Slifer, Alexander G. Bassuk, John A. Kessler, Michael C. Reed, H. Frederik Nijhout, Timothy M. George, David S. Enterline, John R. Gilbert, Marcy C. Speer

    Published 2006
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  15. 15
    Clinical and Pathologic Features of Familial Interstitial Pneumonia

    Clinical and Pathologic Features of Familial Interstitial Pneumonia by Mark P. Steele, Marcy C. Speer, James E. Loyd, Kevin M. Brown, Aretha Herron, Susan H. Slifer, Lauranell H. Burch, Momen M. Wahidi, John A. Phillips, Thomas A. Sporn, H. Page McAdams, Marvin I. Schwarz, David A. Schwartz

    Published 2005
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  16. 16
    Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy

    Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy by Eric J. Horstick, Jeremy W. Linsley, James J. Dowling, Michael A. Hauser, Kristin McDonald Gibson, Allison E. Ashley‐Koch, Louis Saint‐Amant, Akhila Satish, Wilson W. Cui, Weibin Zhou, Shawn M. Sprague, Demetra S. Stamm, Cynthia M. Powell, Marcy C. Speer, Clara Franzini‐Armstrong, Hiromi Hirata, John Y. Kuwada

    Published 2013
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  17. 17
    Myotilin is mutated in limb girdle muscular dystrophy 1A

    Myotilin is mutated in limb girdle muscular dystrophy 1A by Michael A. Hauser, Stephen Horrigan, Paula Salmikangas, Udana Torian, Kristi D. Viles, Ria Dancel, Richard W. Tim, Anu Taivainen, Luria Bartoloni, James M. Gilchrist, Jeffrey M. Stajich, P. C. Gaskell, John R. Gilbert, Jeffery M. Vance, Margaret A. Pericak-Vance, Olli Carpén, Carol A. Westbrook, Marcy C. Speer

    Published 2000
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  18. 18
    A Common<i>MUC5B</i>Promoter Polymorphism and Pulmonary Fibrosis

    A Common<i>MUC5B</i>Promoter Polymorphism and Pulmonary Fibrosis by Max A. Seibold, Anastasia L. Wise, Marcy C. Speer, Mark P. Steele, Kevin M. Brown, James E. Loyd, Tasha E. Fingerlin, Weiming Zhang, Gunnar Guðmundsson, Steve D. Groshong, Christopher M. Evans, Stavros Garantziotis, Kenneth B. Adler, Burton F. Dickey, Roland M. du Bois, Ivana V. Yang, Aretha Herron, Dolly Kervitsky, Janet Talbert, Cheryl Markin, Joungjoa Park, Anne L. Crews, Susan H. Slifer, Scott S. Auerbach, Michelle G. Roy, Jia Lin, Corinne E. Hennessy, Marvin I. Schwarz, David A. Schwartz

    Published 2011
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  19. 19
    Addendum: Standardizing global gene expression analysis between laboratories and across platforms

    Addendum: Standardizing global gene expression analysis between laboratories and across platforms by T K Bammler, Richard P. Beyer, Sanchita Bhattacharya, Gary A. Boorman, Abee L. Boyles, Blair U. Bradford, Roger E. Bumgarner, Pierre R. Bushel, Kabir Chaturvedi, Dongseok Choi, Michael L. Cunningham, Shibing Deng, Holly K. Dressman, Rickie D. Fannin, F M Farin, Jonathan H. Freedman, Rebecca C. Fry, Angel Harper, Michael C. Humble, Patrick Hurban, Terrance J. Kavanagh, William K. Kaufmann, Kathleen F. Kerr, Li Jing, Jodi Lapidus, Michael Lasarev, Jianying Li, Yi‐Ju Li, Edward K. Lobenhofer, Xinfang Lu, Renae L. Malek, Sean Milton, Srinivasa R. Nagalla, Jean O’Malley, Valerie S. Palmer, Patrick Pattee, Richard S. Paules, Charles M. Perou, K L Phillips, Li‐Xuan Qin, Yang Qiu, Sean Quigley, Matthew Rodland, Ivan Rusyn, Leona D. Samson, David A. Schwartz, Yan Shi, Jung-Lim Shin, Stella O. Sieber, Susan Slifer, Marcy C. Speer, Peter S. Spencer, Dean I. Sproles, James A. Swenberg, William A. Suk, Robert Sullivan, Ru Tian, Raymond W. Tennant, Signe A. Todd, Charles J. Tucker, Bennett Van Houten, Brenda K. Weis, Shirley Xuan, Helmut Zarbl

    Published 2005
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