Two Radiation-Induced Chromosomal Inversions in Mice (Mus musculus)

per Roderick, Thomas H., Hawes, Norman L.
Publicat 1970

Nineteen Paracentric Chromosomal Inversions in Mice

per Roderick, Thomas H., Hawes, Norman L.
Publicat 1974

Genetic Background Modifies Inner Ear and Eye Phenotypes of Jag1 Heterozygous Mice

per Kiernan, Amy E., Li, Renhua, Hawes, Norman L., Churchill, Gary A., Gridley, Thomas
Publicat 2007

The Bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization

per Smith, Richard S., John, Simon W. M., Zabeleta, Adriana, Davisson, Muriel T., Hawes, Norman L., Chang, Bo
Publicat 2000

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation

per Anderson, Michael G., Hawes, Norman L., Trantow, Colleen M., Chang, Bo, John, Simon W.M.
Publicat 2007

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene

per Johnson, Kenneth R., Gagnon, Leona H., Webb, Lisa S., Peters, Luanne L., Hawes, Norman L., Chang, Bo, Zheng, Qing Yin
Publicat 2003

Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice

per Talamas, Elijah, Jackson, Lavinia, Koeberl, Matthew, Jackson, Todd, McElwee, John L., Hawes, Norman L., Chang, Bo, Jablonski, Monica M., Sidjanin, D.J.
Publicat 2006

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

per Anderson, Michael G, Smith, Richard S, Savinova, Olga V, Hawes, Norman L, Chang, Bo, Zabaleta, Adriana, Wilpan, Robert, Heckenlively, John R, Davisson, Muriel, John, Simon WM
Publicat 2001

Restoration of cone vision in a mouse model of achromatopsia

per Alexander, John J, Umino, Yumiko, Everhart, Drew, Chang, Bo, Min, Seok H, Li, Qiuhong, Timmers, Adrian M, Hawes, Norman L, Pang, Ji-jing, Barlow, Robert B, Hauswirth, William W
Publicat 2007

Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent

per Young, Kelly A., Berry, Melissa L., Mahaffey, Connie L., Saionz, Jennifer R., Hawes, Norman L., Chang, Bo, Zheng, Qing Yin, Smith, Richard S., Bronson, Roderick T., Nelson, Randy J., Simpson, Elizabeth M.
Publicat 2002

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure

per Chang, Bo, Smith, Richard S, Peters, Maureen, Savinova, Olga V, Hawes, Norman L, Zabaleta, Adriana, Nusinowitz, Steven, Martin, Janice E, Davisson, Muriel L, Cepko, Constance L, Hogan, Brigid LM, John, Simon WM
Publicat 2001

AAV-Mediated Gene Therapy for Retinal Degeneration in the rd10 Mouse Containing a Recessive PDEβ Mutation

per Pang, Ji-jing, Boye, Sanford L., Kumar, Ashok, Dinculescu, Astra, Deng, Wentao, Li, Jie, Li, Qiuhong, Rani, Asha, Foster, Thomas C., Chang, Bo, Hawes, Norman L., Boatright, Jeffrey H., Hauswirth, William W.
Publicat 2008

A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

per DONAHUE, LEAH RAE, CHANG, BO, MOHAN, SUBBURAMAN, MIYAKOSHI, NAO, WERGEDAL, JON E, BAYLINK, DAVID J, HAWES, NORMAN L, ROSEN, CLIFFORD J, WARD-BAILEY, PATRICIA, ZHENG, QING Y, BRONSON, RODERICK T, JOHNSON, KENNETH R, DAVISSON, MURIEL T
Publicat 2003

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

per Akhmedov, Novrouz B., Piriev, Natik I., Chang, Bo, Rapoport, Ana Lia, Hawes, Norman L., Nishina, Patsy M., Nusinowitz, Steven, Heckenlively, John R., Roderick, Thomas H., Kozak, Christine A., Danciger, Michael, Davisson, Muriel T., Farber, Debora B.
Publicat 2000

Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration

per Friedman, James S. , Chang, Bo , Kannabiran, Chitra , Chakarova, Christina , Singh, Hardeep P. , Jalali, Subhadra , Hawes, Norman L. , Branham, Kari , Othman, Mohammad , Filippova, Elena , Thompson, Debra A. , Webster, Andrew R. , Andréasson, Sten , Jacobson, Samuel G. , Bhattacharya, Shomi S. , Heckenlively, John R. , Swaroop, Anand 
Publicat 2006

Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene

per Chang, Bo, Mandal, Md Nawajes A., Chavali, Venkata R.M., Hawes, Norman L., Khan, Naheed W., Hurd, Ronald E., Smith, Richard S., Davisson, Muriel L., Kopplin, Laura, Klein, Barbara E.K., Klein, Ronald, Iyengar, Sudha K., Heckenlively, John R., Ayyagari, Radha
Publicat 2008

Allelic variance between GRM6 mutants, Grm6(nob3) and Grm6(nob4) results in differences in retinal ganglion cell visual responses

per Maddox, Dennis M, Vessey, Kirstan A, Yarbrough, Gary L, Invergo, Brandon M, Cantrell, Donald R, Inayat, Samsoon, Balannik, Victoria, Hicks, Wanda L, Hawes, Norman L, Byers, Shannon, Smith, Richard S, Hurd, Ron, Howell, Douglas, Gregg, Ronald G., Chang, Bo, Naggert, Jürgen K, Troy, John B, Pinto, Lawrence H, Nishina, Patsy M, McCall, Maureen A
Publicat 2008