Lysosomal Dysfunctions Associated with Mutations at Mouse Pigment Genes

Por Novak, Edward K., Swank, Richard T.
Publicado em 1979

Mutation of a transcriptional motif of a distant regulatory element reduces the expression of embryonic and fetal globin genes

Por Navas, Patrick A., Swank, Richard A., Yu, Man, Peterson, Kenneth R., Stamatoyannopoulos, George
Publicado em 2003

Murine Leukemia Virus Spreading in Mice Impaired in the Biogenesis of Secretory Lysosomes and Ca(2+)-Regulated Exocytosis

Por Chan, Wai-Tsing, Sherer, Nathan M., Uchil, Pradeep D., Novak, Edward K., Swank, Richard T., Mothes, Walther
Publicado em 2008

Defective Surfactant Secretion in a Mouse Model of Hermansky-Pudlak Syndrome

Por Guttentag, Susan H., Akhtar, Amana, Tao, Jian-Qin, Atochina, Elena, Rusiniak, Michael E., Swank, Richard T., Bates, Sandra R.
Publicado em 2005

A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11

Por Mohlke, Karen L., Nichols, William C., Westrick, Randal J., Novak, Edward K., Cooney, Kathleen A., Swank, Richard T., Ginsburg, David
Publicado em 1996

The gene for the muted (mu) mouse, a model for Hermansky–Pudlak syndrome, defines a novel protein which regulates vesicle trafficking

Por Zhang, Qing, Li, Wei, Novak, Edward K., Karim, Amna, Mishra, Vishnu S., Kingsmore, Stephen F., Roe, Bruce A., Suzuki, Tamio, Swank, Richard T.
Publicado em 2002

The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation

Por Suzuki, Tamio, Oiso, Naoki, Gautam, Rashi, Novak, Edward K., Panthier, Jean-Jacques, Suprabha, P. G., Vida, Thomas, Swank, Richard T., Spritz, Richard A.
Publicado em 2003

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice

Por Wilson, Scott M., Yip, Richard, Swing, Deborah A., O'Sullivan, T. Norene, Zhang, Yuke, Novak, Edward K., Swank, Richard T., Russell, Liane B., Copeland, Neal G., Jenkins, Nancy A.
Publicado em 2000

The Vps33a gene regulates behavior and cerebellar Purkinje cell number

Por Chintala, Sreenivasulu, Novak, Edward K., Spernyak, Joseph A., Mazurchuk, Richard, Torres, German, Patel, Suchith, Busch, Kristie, Meeder, Beth A., Horowitz, Judith M., Vaughan, Mary M., Swank, Richard T.
Publicado no Brain Res (2009)

The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules

Por Chintala, Sreenivasulu, Tan, Jian, Gautam, Rashi, Rusiniak, Michael E., Guo, Xiaoli, Li, Wei, Gahl, William A., Huizing, Marjan, Spritz, Richard A., Hutton, Saunie, Novak, Edward K., Swank, Richard T.
Publicado em 2007

Involvement of Vps33a in the Fusion of Uroplakin-Degrading Multivesicular Bodies with Lysosomes

Por Guo, Xuemei, Tu, Liyu, Gumper, Iwona, Plesken, Heide, Novak, Edward K., Chintala, Sreenivasulu, Swank, Richard T., Pastores, Gregory, Torres, Paola, Izumi, Tetsuro, Sun, Tung-Tien, Sabatini, David D., Kreibich, Gert
Publicado no Traffic (2009)

Rab geranylgeranyl transferase α mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis

Por Detter, John C., Zhang, Qing, Mules, Emilie H., Novak, Edward K., Mishra, Vishnu S., Li, Wei, McMurtrie, Elzbieta B., Tchernev, Velizar T., Wallace, Margaret R., Seabra, Miguel C., Swank, Richard T., Kingsmore, Stephen F.
Publicado em 2000

Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells

Por Chintala, Sreenivasulu, Li, Wei, Lamoreux, M. Lynn, Ito, Shosuke, Wakamatsu, Kazumasa, Sviderskaya, Elena V., Bennett, Dorothy C., Park, Young-Mee, Gahl, William A., Huizing, Marjan, Spritz, Richard A., Ben, Songtao, Novak, Edward K., Tan, Jian, Swank, Richard T.
Publicado em 2005

The mouse pale ear (ep) mutation is the homologue of human Hermansky–Pudlak syndrome

Por Gardner, John M., Wildenberg, Scott C., Keiper, Natalie M., Novak, Edward K., Rusiniak, Michael E., Swank, Richard T., Puri, Neelu, Finger, Joshua N., Hagiwara, Nobuko, Lehman, Anne L., Gales, Tracy L., Bayer, Manfred E., King, Richard A., Brilliant, Murray H.
Publicado em 1997

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

Por Li, Wei, Zhang, Qing, Oiso, Naoki, Novak, Edward K, Gautam, Rashi, O'Brien, Edward P, Tinsley, Caroline L, Blake, Derek J, Spritz, Richard A, Copeland, Neal G, Jenkins, Nancy A, Amato, Dominick, Roe, Bruce A, Starcevic, Marta, Dell'Angelica, Esteban C, Elliott, Rosemary W, Mishra, Vishnu, Kingsmore, Stephen F, Paylor, Richard E, Swank, Richard T
Publicado em 2003