International Mammalian Genome Society

F. Gene Discovery

Presentations

1. Mutation of the Na-K-Cl Cotransporter Gene Slc12a2 in Shaker-with-Syndactylism Mutants
   Karen P. Steel, James Gazzard, Shazia Chaudhry, Natalie Sampson, Bradley A. Schulte, and Michael J Dixon
2. Positional Cloning of the Gunmetal Mouse Mutation
   John C. Detter, Stephen Kingsmore
3. Positional Cloning of the Pallid Gene Reveals a Novel, Syntaxin 13-Interacting Protein Involved in Platelet Storage Pool Deficiency
   Liping Huang, Yien-Ming Kuo, and Jane Gitschier,
4. Mutation by Generation of a Novel Hybrid Gene in the Neurological Mutant flailer
   Julie M. Jones, Jian-Dong Huang, Valerie Mermall, Bruce Hamilton, Mark S. Mooseker, Andrew Escayg, Neal G. Copeland, Nancy A. Jenkins and Miriam H. Meisler
5. A. New Resources for Mouse Biology and Genetics
   James F. Battey, Jr., Director, NIDOCD, NIH Co-Chair, Trans-NIH Mouse Genomics and Genetics Resources Coordinating Group
   no abstract available
   B. All Sperm are Created Equal, But Smoks Make Them Behave Different
   Bernhard Herrmann, Department of Developmental Biology, Max-Planck Institue of Immunology, Freiburg, Germany
   no abstract available
6. Modeling Cancer in the Mouse: Rapid Proviral Tagging of Novel Proto-Oncogenes Responsible for the Development of B-Cell Leukemia
   Monica J. Justice, Gwenn M. Hansen, Darlene Skapura, and Alex George
7. Genetic and Biochemical Studies of the Mahogany Gene
   Gunn, T.M., He, L., Duke-Cohan, J., and Barsh, G
8. The LOBO Gene Generates Extraordinary Long Bones in Transgenic Mice and is a Candidate Gene for Albright Hereditary Osteodystrophy
   Andreas Rump, Jochen Hess, Thomas Aigner, Thomas Liehr, Andre Rosenthal, Thomas Wirth

Posters

9. Gene Discovery: Novel Mouse and Human ß-Defensins
   David Adler, James Holloway, Scott Presnell, Paul Sheppard, Nand Banduir, Mark Rixon, Zeren Gao, Betty Haldeman, Dao Mai, Kathleen M. Walker and Stephanie Beigel
10. Ts65Dn - A Mouse Model for Down Syndrome
    Muriel T. Davisson, Lawrence J. Bechtel, Cecilia Schmidt, Roderick T. Bronson, and Alberto C. S. Costa
11. Progress Towards the High Resolution Mapping of nackt: A Novel Mouse Mutation Affecting Hair Growth and CD4⁺ T Cells Development
    Fernando Benavides, Natalia Martin Palenzuela, Jean Jaubert, Jean-Louis Guénet, Claudio J. Conti
12. Genetic and Physical Mapping of the Mouse Myelencephalic Blebs and Blebbed Mutations
    Liz Bentley and Susan M. Darling
13. Evaluation of New Candidate Genes Isolated by Positional Cloning Strategies for the Plasmacytoma Susceptibility/Resistance Gene, Pctr2
    Valery Bliskovsky, Edward S. Ramsay, Shuling Zhang, Rebecca Liddell & Beverly A. Mock
14. crsp - A New Mouse Trasgene Insertional Mutation Causing Cryptorchidism
    C. E. Bishop, P. A. Overbeek, J. B. Houston, R. Sutherland, H. L. Boettger-Tong, A. I. Agulnik
15. withdrawn
16. Functional, structural and genetic analyses of waltzer (v) and mdfw
    Elizabeth Bryda, Konrad Noben-Trauth, Hung J. Kim, Ralph H. Holme and Karen P. Steel
17. Humanizing the Mouse a-synuclein Locus - Development of Mouse Models for Parkinson's Disease
    Cabin, D., S. Gispert, B. Orrison, A. Chen, L. Garrett and R. Nussbaum.
18. Genetic Mapping of the Bent Tail Mutation and the Identification of a Small X Chromosomal Deletion Associated with the Mutation
    Carrel, T. L., Wilbur Harrison and Frederick Elder, and Herman, G. E
19. Fine Mapping of the Osteopetrotic Grey-Lethal Locus on Mouse Chromosome 10
    Nader Chalhoub, Hugues Bernard and Jean Vacher
20. Progress in Characterization of a Recessive Lethal Mutant Near the D17Aus9 Locus
    Hanna Chao, Sarah Mentzer, Rebecca Bergstrom, John Schimenti, and Yun You
21. Genomic Characterization and Targeted Mutagenesis of Lysophosphatidic Acid Receptor Genes (lp_A1/lp_A2/lp_A3)
    James J. A. Contos and Jerold Chun
22. Genetic Analysis of the Regulatory System Controlling the Induction of Brown Adipocytes in White Fat Tissues
    Ann Allen Coulter, Robert A. Koza, Wolfgang Hofmann and Leslie P. Kozak
23. Cloning and Characterization of Glas-1, A Novel Gene Associated with Mouse Osteopetrosis
    Mathieu Ferron, Hugues Bernard and Jean Vacher
24. Fine Mapping and FISH Analysis of a Mouse T(2;13) Translocation Causing Neurological, Coat Color and Developmental Abnormalities
    Mary Guarnieri, Nestor Cacheiro and Lorraine Flaherty
25. An Integrated Genetic and Physical Map Around the Doublefoot Locus on Mouse Chromosome 1
    Christopher Hayes, Mark Harrison, Gillian Morriss-Kay, Mary Lyon, Steve DM Brown
26. Altered Expression of Pten is an Essential Event in Mouse Thymic Lymphomagenesis
    Michel Herranz, Javier Santos, Mónica Fernández, Janet Reyes, Concepción Vaquero, and José Fernández-Piqueras.
27. Characterization of a Phenocopy of Waved Mice
    Bruce Herron, Lisa Pacella, Dorothee Foernzler, Cherie VanDoren, and David Beier
28. Isolation and Evaluation of Candidate Genes for the High Growth (hg) Mutation in Mice
    Simon Horvat, Jim McWhir, Brad A. Freking, Juan F. Medrano
29. Mutation in the cbA3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse
    J. Graw, J. Löster, A. Reis, E. Wolf, R. Balling, M. Hrabé de Angelis
30. Functional and Genetic Analyses of the Jerker (je) Mouse Mutant
    Torrance K. Jackson and Konrad Noben-Trauth
31. Three New Allelic Mouse Mutations that Cause Skeletal Overgrowth Involve the Natriuretic Peptide Receptor C Gene (Npr3)
    Jean Jaubert, Francis Jaubert, Natalia Martin, Linda L. Washburn, Barbara K. Lee, Eva M. Eicher, and Jean-Louis Guenet
32. Mapping and Manipulation of the Murine Ryanodine Receptor Locus (Ryr1)
    P. Kathirvel, E. Hitchin, R. Ansell, J. McWhir, J. D. Ansell and A. L. Archibald
33. Alymphoplasia is Caused by a Point Mutation in NF-Kappa B Inducing Kinase (NIK) Gene
    Kazuhiro Kitada, Reiko Shinkura, Fumihiko Matsuda, Kei Tashiro, Kouichi Ikita, Katsumi Kogishi, Misao Suzuki, Sigeki Miyawaki, Tasuku Hpnjo, Tadao Serikawa
34. Progress in Genetic and Functional Characterization of Two Mouse Deafness Mutants, pirouette and spinner
    David C. Kohrman, Hana Odeh , Kristina Hunker, Ellen Hibbard, Lisa Beyer, Gary Dootz, Nobuko Hagiwara, Murray H. Brilliant, David F. Dolan, and Yehoash Raphael;
35. Positional Cloning of Two Tumor Suppressor Genes Involved in Gamma-Ray Induced Mouse Thymic Lymphomas
    Kominami R., Okano H., Matsuki A., Wakabayashi Y., Shinbo T., Kosugi S., Takahashi Y., and Niwa O
36. p53 modifiers near the D16Mit181 locus on chromosome 16 and in the vicinity of D19Mit123 on chromosome 19
    Saito Y., Matsuki A., Wakabayashi Y., Kosugi S., Takahashi Y., and Niwa O, and Kominami R
37. Localization of a Breakpoint of Chromosomal Inversion Responsible for the Hairy Ears (Eh) Mutation
    Tetsuo Kunieda, Izumi Ojika, Miyuki Nakamura
38. Positional Cloning of the Flexed-Tail Locus
    Laurie E. Lenox and Robert F. Paulson
39. The stargazer Gene Product is One Member of a Family of Gamma Subunits of Voltage Dependent Calcium Channels
    Verity A. Letts, Connie L. Mahaffey and Wayne N. Frankel
40. High-Resolution Mapping and Transcript Identification at the sdy Locus on Mouse Chromosome 13
    Wei Li, Vishnu S. Mishra, Yuke Zhang, Qing Zhang, Edward K. Novak, Nancy A. Jenkins, Neal G. Copeland, Stephen F. Kingsmore, Richard T. Swank
41. Characterization of the Deaf Mouse Mutant, jackson circler (jc)
    Michelle L. Mack and Konrad Noben-Trauth
42. A Deletion Found in the Copper-Transporting P-type ATPase Gene in the Pewter Mutation
    Jingfang Niu, Frank A. Verley, Susan L. Dagenais and Thomas W.Glover
43. Characterisation of a Mouse Model of Neuromuscular Disease Generated by Transgenic Insertional Mutagenesis
    Derek Paisley and Andrew Ward
44. Towards the Positional Cloning of the Mouse Deafness Mutant Quivering
    N. J. Parkinson, J. McKee-Johnson, V. A. Street, C. Olsen, B. L. Tempel
45. Characterization of the Friend Virus Susceptibility Gene 2 (Fv2) Locus on Mouse Chromosome 9
    Pam Correll, Ed Melkin, Paul Ney and Robert Paulson
46. Isolation and Characterization of a Candidate for the Mouse Hybrid Sterilitiy 6 Gene
    Steve Pilder, John Fossella, Sadhana Samant, Lee Silver
47. Genetic and Physical Mapping of Hague (Hag), A Mouse Hair Mutation with Unusual Transmission
    Christophe Poirier, Atsushi Yoshiki, and Moriaki Kusakabe
48. Molecular Genetic Analysis of a Transgene-Induced Allele of Oligosyndactylism
    Dimitrina D. Pravtcheva and Thomas L. Wise
49. Molecular Cloning and Sequencing of the HRC Gene from Mouse Heart Reveals a Highly Unstable GAG Repeat
    Shundi Shi, Steven R. Brunnert
50. Bradyarrhythmias and Congestive Heart Failure in the Mice Defective in the M1 Muscarinic Receptor/PLC-1 Signaling
    Woo, S-H., Hwang, J-Y., Kim, S-S., Lee, B-H., Namkung, Y., Lee, C-O., Kim, D., and Shin, H-S.
51. Mapping of the SCNM1 Modifier Locus Responsible for Dystonia in Sodium Channel Deficient Mice and Development of SCN8A Congenic Strains
    Leslie K. Sprunger and Miriam H. Meisler
52. Identifying Interacting Partners to the Mouse Myosin VIIA Protein Involved in Genetic Deafness
    Penio Todorov, Rachel E. Hardisty, Karen P. Steel and Steve D.M. Brown
53. Isolation of a Novel Cochlear Transcript from the wi Region of Mouse Chromosome 4
    H. T. Tsai, P. Mburu, R. E. Hardisty, A. Varela, A. J. W. Paige, B. W. Kiernan, J. Fleming, M. Rogers, K. P. Steel and S. D. M. Brown
54. A Lupus Susceptibility Locus Present in C57BL/10, But Not C57BL/6, Mice
    Rebecca Tucker, Stephen Rozzo, Brian Kotzin
55. The Identification of a Candidate Gene for the wi Deafness Mutant
    A. Varela, P. Mburu, R. E. Hardisty, H. T. Tsai, A. J. W. Paige, B. W. Kiernan, R. H. Holme, J. Fleming, M. J. C. Rogers, K. P. Steel and S. D. M. Brown
56. A Deletion Found in the Copper-Transporting P-Type ATPase Gene in the Pewter Mutation
    Jingfang Niu, Frank A. Verley, Susan Dagenais, and Tom Glover
57. Physical Mapping in the psr Region of Mouse Chromosome 7
    Lisa S. Webb, Madhu S. Dhar, and Dabney K. Johnson
58. Mapping of Loa, A Mouse Motor Deficit Mutation, to Distal Chromosome 12
    Witherden, A. S., Nicholson, S. J., Hafezparast, M., Bermingham, N. A., Peters, J., Ball, S. T., Rogers, D. C., Martin, J. E. and Fisher, E. M. C
59. Development of a Mouse Model for Hereditary Hemorrhagic Telangiectasia Type II
    Jing Yu, Roger McLendon, En Li, Paul Oh, Travis J., Riney, Rosemary Akhurst, Robert J. Lechleider, Austin Diamond, Helen Arthur, Raju Kucherlapati, Winfried Edelmann, Marie Lia, Doug Marchuk