Хайлтын үр дүнгүүд - Marcy C. Speer
- 19-н 1 - 19 үр дүнгүүдийг харуулж байна
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Candidate gene analysis in human neural tube defects -н Abee L. Boyles, Preston Hammock, Marcy C. Speer
Хэвлэсэн 2005Revisão -
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Human neural crest cells display molecular and phenotypic hallmarks of stem cells -н Sophie Thomas, Marie Thomas, Patrick Wincker, Candice Babarit, Pu‐Ting Xu, Marcy C. Speer, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Heather Etchevers
Хэвлэсэн 2008Artigo -
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Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations -н Christina A. Markunas, R. Shane Tubbs, Roham Moftakhar, Allison E. Ashley‐Koch, Simon G. Gregory, W. Jerry Oakes, Marcy C. Speer, Bermans J. Iskandar
Хэвлэсэн 2012Artigo -
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Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics -н 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
Хэвлэсэн 2003Artigo -
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Linkage Disequilibrium Inflates Type I Error Rates in Multipoint Linkage Analysis when Parental Genotypes Are Missing -н 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
Хэвлэсэн 2005Artigo -
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Gene Expression Profiling of Familial and Sporadic Interstitial Pneumonia -н 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
Хэвлэсэн 2006Artigo -
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Allelic and locus heterogeneity in inherited venous malformations -н 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
Хэвлэсэн 1999Artigo -
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Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions -н 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
Хэвлэсэн 2006Artigo -
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Clinical and Pathologic Features of Familial Interstitial Pneumonia -н 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
Хэвлэсэн 2005Artigo -
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Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy -н 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
Хэвлэсэн 2013Artigo -
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Myotilin is mutated in limb girdle muscular dystrophy 1A -н 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
Хэвлэсэн 2000Artigo -
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A Common<i>MUC5B</i>Promoter Polymorphism and Pulmonary Fibrosis -н 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
Хэвлэсэн 2011Artigo -
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Addendum: Standardizing global gene expression analysis between laboratories and across platforms -н 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
Хэвлэсэн 2005Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Medicine
Genotype
Internal medicine
Allele
Embryo
Pathology
Population
Anatomy
Chiari malformation
Endocrinology
Locus (genetics)
Lung
Magnetic resonance imaging
Missense mutation
Muscular dystrophy
Myopathy
Neural tube
Phenotype
Radiology
Single-nucleotide polymorphism
Syringomyelia
Anencephaly
Candidate gene
Cell biology
Chiari I malformation
Computational biology
Demography