Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4 von Newton, J.M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.

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Posterior staphyloma in oculocutaneous albinism: another possible cause of reduced visual acuity von Lee, Susan, BSN, Schimmenti, Lisa A., MD, King, Richard A., MD, PhD, Brilliant, Murray, PhD, Anderson, Jennifer L., BS, Schoonveld, Cheri, MS, CGC, Summers, C. Gail, MD

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Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype von KING, Richard A, PIETSCH, Jacy, FRYER, James P, SAVAGE, Sarah, BROTT, Marcia J, RUSSELL-EGGITT, Isabelle, SUMMERS, C. Gail, OETTING, William S

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Genomewide Screen and Identification of Gene-Gene Interactions for Asthma-Susceptibility Loci in Three U.S. Populations: Collaborative Study on the Genetics of Asthma von Xu, Jianfeng, Meyers, Deborah A., Ober, Carole, Blumenthal, Malcolm N., Mellen, Beverly, Barnes, Kathleen C., King, Richard A., Lester, Lucille A., Howard, Timothy D., Solway, Julian, Langefeld, Carl D., Beaty, Terri H., Rich, Stephen S., Bleecker, Eugene R., Cox, Nancy J.

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ER-to-Golgi transport and SEC23-dependent COPII vesicles regulate T cell alloimmunity von Kim, Stephanie, Khoriaty, Rami, Li, Lu, McClune, Madison, Kalfa, Theodosia A., Wu, Julia, Peltier, Daniel, Fujiwara, Hideaki, Sun, Yaping, Oravecz-Wilson, Katherine, King, Richard A., Ginsburg, David, Reddy, Pavan

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MC1R Mutations Modify the Classic Phenotype of Oculocutaneous Albinism Type 2 (OCA2) von King, Richard A., Willaert, Rebecca K., Schmidt, Ramona M., Pietsch, Jacy, Savage, Sarah, Brott, Marcia J., Fryer, James P., Summers, C. Gail, Oetting, William S.

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Pedagogical Content Knowing: An Integrative Model for Teacher Preparation von Cochran, Kathryn F., DeRuiter, James A., King, Richard A.

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Gene Expression Profiling in Murine Obliterative Airway Disease von Lande, Jeffrey D., Dalheimer, Stacy L., Mueller, Daniel L., Hertz, Marshall I., King, Richard A.

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Molecular basis of albinism: Mutations and polymorphisms of pigmentation genes associated with albinism von Oetting, William S., King, Richard A.

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Genetic Analysis of Mammographic Breast Density in Adult Women: Evidence of a Gene Effect von Pankow, James S., Vachon, Celine M., Kuni, Christopher C., King, Richard A., Arnett, Donna K., Grabrick, Dawn M., Rich, Stephen S., Anderson, V. Elving, Sellers, Thomas A.

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New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17 von Paluru, Prasuna, Ronan, Shawn M, Heon, Elise, Devoto, Marcella, Wildenberg, Scott C, Scavello, Genaro, Holleschau, Ann, Makitie, Outi, Cole, William G, King, Richard A, Young, Terri L

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Designing Finance Structures to Satisfy Equity and Adequacy Goals von King, Richard A., Swanson, Austin D., Sweetland, Scott R.

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P gene mutations associated with oculocutaneous albinism type II (OCA2) von Oetting, William S., Garrett, Sarah Savage, Brott, Marcia, King, Richard A.

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Bronchoalveolar Lavage Cell Gene Expression in Acute Lung Rejection : Development of a Diagnostic Classifier von PATIL, Jagadish, LANDE, Jeffrey D, NA LI, BERRYMAN, Todd R, KING, Richard A, HERTZ, Marshall

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Visualizing Human Leukocyte Antigen Class II Risk Haplotypes in Human Systemic Lupus Erythematosus von Graham, Robert R., Ortmann, Ward A., Langefeld, Carl D., Jawaheer, Damini, Selby, Scott A., Rodine, Peter R., Baechler, Emily C., Rohlf, Kristine E., Shark, Katherine B., Espe, Karl J., Green, Linda E., Nair, Rajan P., Stuart, Philip E., Elder, James T., King, Richard A., Moser, Kathy L., Gaffney, Patrick M., Bugawan, Teodorica L., Erlich, Henry A., Rich, Stephen S., Gregersen, Peter K., Behrens, Timothy W.

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Variation in the Interleukin 4–Receptor α Gene Confers Susceptibility to Asthma and Atopy in Ethnically Diverse Populations von Ober, Carole, Leavitt, Stephanie A., Tsalenko, Anya, Howard, Timothy D., Hoki, Danessa M., Daniel, Rajeev, Newman, Dina L., Wu, Xiaodong, Parry, Rodney, Lester, Lucille A., Solway, Julian, Blumenthal, Malcolm, King, Richard A., Xu, Jianfeng, Meyers, Deborah A., Bleecker, Eugene R., Cox, Nancy J.

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Spectrum of Foveal Development in Albinism Detected with Optical Coherence Tomography von Harvey, Patti S., King, Richard A., Summers, C. Gail

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A Genome-Wide Search for Susceptibility Genes in Human Systemic Lupus Erythematosus Sib-Pair Families von Gaffney, Patrick M., Kearns, Grainne M., Shark, Katherine B., Ortmann, Ward A., Selby, Scott A., Malmgren, Michelle L., Rohlf, Kristine E., Ockenden, Theresa C., Messner, Ronald P., King, Richard A., Rich, Stephen S., Behrens, Timothy W.

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The R402Q tyrosinase variant does not cause autosomal recessive ocular albinism von Oetting, William S., Pietsch, Jacy, Brott, Marcia J., Savage, Sarah, Fryer, James P., Summers, C. Gail, King, Richard A.

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Gene Expression Profiling of Bronchoalveolar Lavage Cells in Acute Lung Rejection von Gimino, Vincent J, Lande, Jeffrey D, Berryman, Todd R, King, Richard A, Hertz, Marshall I

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