Witch Nails (Krt90whnl): A spontaneous mouse mutation affecting nail growth and development von Sundberg, John P, Galantino-Homer, Hannah, Fairfield, Heather, Ward-Bailey, Patricia F, Harris, Belinda S, Berry, Melissa, Pratt, C Herbert, Gott, Nicholas E, Bechtold, Lesley S, Kaplan, Pauline R, Durbin-Johnson, Blythe P, Rocke, David M, Rice, Robert H

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Ectopic Mineralization and Conductive Hearing Loss in Enpp1asj Mutant Mice, a New Model for Otitis Media and Tympanosclerosis von Tian, Cong, Harris, Belinda S, Johnson, Kenneth R

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Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP von Ackerman, Susan L, Zhao, Lihong, Longo-Guess, Chantal, Harris, Belinda S, Lee, Jeong-Woong

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A novel mouse Dscam mutation inhibits localization and shedding of DSCAM von Schramm, R Dee, Li, Shuai, Harris, Belinda S, Rounds, Ryan P, Burgess, Robert W, Ytreberg, F Marty, Fuerst, Peter G

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Purkinje Cell Degeneration (pcd) Phenotypes Caused by Mutations in the Axotomy-Induced Gene, Nna1 von Fernandez-Gonzalez, Angeles, La Spada, Albert R., Treadaway, Jason, Higdon, Jason C., Harris, Belinda S., Sidman, Richard L., Morgan, James I., Zuo, Jian

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Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass von Munroe, Robert J, Prabhu, Vinay, Acland, Greg M, Johnson, Kenneth R, Harris, Belinda S, O'Brien, Tim P, Welsh, Ian C, Noden, Drew M, Schimenti, John C

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RREB1 regulates neuronal proteostasis and the microtubule network von Griffin, Emily N, Jucius, Thomas, Sim, Su-Eon, Harris, Belinda S, Heinz, Sven, Ackerman, Susan L

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Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders von Fairfield, Heather, Srivastava, Anuj, Ananda, Guruprasad, Liu, Rangjiao, Kircher, Martin, Lakshminarayana, Anuradha, Harris, Belinda S, Karst, Son Yong, Dionne, Louise A, Kane, Coleen C, Curtain, Michelle, Berry, Melissa L, Ward-Bailey, Patricia F, Greenstein, Ian, Byers, Candice, Czechanski, Anne, Sharp, Jocelyn, Palmer, Kristina, Gudis, Polyxeni, Martin, Whitney, Tadenev, Abby, Bogdanik, Laurent, Pratt, C Herbert, Chang, Bo, Schroeder, David G, Cox, Gregory A, Cliften, Paul, Milbrandt, Jeffrey, Murray, Stephen, Burgess, Robert, Bergstrom, David E, Donahue, Leah Rae, Hamamy, Hanan, Masri, Amira, Santoni, Federico A, Makrythanasis, Periklis, Antonarakis, Stylianos E, Shendure, Jay, Reinholdt, Laura G

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A novel null allele of mouse DSCAM survives to adulthood on an inbred C3H background with reduced phenotypic variability von Fuerst, Peter G., Harris, Belinda S., Johnson, Kenneth R., Burgess, Robert W.

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Hearing Impairment in Hypothyroid Dwarf Mice Caused by Mutations of the Thyroid Peroxidase Gene von Johnson, Kenneth R., Gagnon, Leona H., Longo-Guess, Chantal M., Harris, Belinda S., Chang, Bo

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podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development von Mao, Mao, Thedens, Daniel R, Chang, Bo, Harris, Belinda S, Zheng, Qing Yin, Johnson, Kenneth R, Donahue, Leah Rae, Anderson, Michael G

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Dsprul: A spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome von Herbert Pratt, C., Potter, Christopher S., Fairfield, Heather, Reinholdt, Laura G., Bergstrom, David E., Harris, Belinda S., Greenstein, Ian, Dadras, Soheil S., Liang, Bruce T., Schofield, Paul N., Sundberg, John P.

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A novel null allele of mouse Dscam survives to adulthood on an inbred C3H background with reduced phenotypic variability von Fuerst, Peter G., Harris, Belinda S., Johnson, Kenneth R., Burgess, Robert W.

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Ectopic Mineralization and Conductive Hearing Loss in Enpp1.sup.asj Mutant Mice, a New Model for Otitis Media and Tympanosclerosis von Tian, Cong, Harris, Belinda S, Johnson, Kenneth R

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Witch Nails von Sundberg, John P, Galantino-Homer, Hannah, Fairfield, Heather, Ward-Bailey, Patricia F, Harris, Belinda S, Berry, Melissa, Pratt, C. Herbert, Gott, Nicholas E, Bechtold, Lesley S, Kaplan, Pauline R, Durbin-Johnson, Blythe P, Rocke, David M, Rice, Robert H

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Curly bare ( cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene ( mcub) on chromosome 5 von Johnson, Kenneth R, Lane, Priscilla W, Cook, Susan A, Harris, Belinda S, Ward-Bailey, Patricia F, Bronson, Roderick T, Lyons, Bonnie L, Shultz, Leonard D, Davisson, Muriel T

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Grey intense: a new mouse mutation affecting pigmentation von Davisson, M T, Johnson, K R, Bronson, R T, Ward-Bailey, P F, Cook, S A, Harris, B S, Donahue, L R

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Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17 von Smith, R S, Johnson, K R, Hawes, N L, Harris, B S, Sundberg, J P, Davisson, M T

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Dsp rul: a spontaneous mouse mutation in desmoplakin as a model of Carvajal-Huerta syndrome von Herbert Pratt, C, Potter, Christopher S, Fairfield, Heather, Reinholdt, Laura G, Bergstrom, David E, Harris, Belinda S, Greenstein, Ian, Dadras, Soheil S, Liang, Bruce T, Schofield, Paul N, Sundberg, John P

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Thrombocytopenia and Cardiomyopathy (trac): A New Single Gene Mutation Resulting in Severe Platelet and Heart Abnormalities in Mice von Shultz, Leonard D., Lyons, Bonnie L., Bronson, Roderick T., Donahue, Leah Rae, Burzenski, Lisa M., Gott, Bruce, Harris, Belinda S., Italiano, Joseph E., Johnson, Kenneth R.

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