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

Por Roderick, Thomas H., Hawes, Norman L.
Publicado em 1970

Nineteen Paracentric Chromosomal Inversions in Mice

Por Roderick, Thomas H., Hawes, Norman L.
Publicado em 1974

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

Por Kiernan, Amy E., Li, Renhua, Hawes, Norman L., Churchill, Gary A., Gridley, Thomas
Publicado em 2007

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

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

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation

Por Anderson, Michael G., Hawes, Norman L., Trantow, Colleen M., Chang, Bo, John, Simon W.M.
Publicado em 2007

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

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

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

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

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

Por 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
Publicado em 2001

Restoration of cone vision in a mouse model of achromatopsia

Por 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
Publicado em 2007

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

Por 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.
Publicado em 2002

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

Por 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
Publicado em 2001

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

Por 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.
Publicado em 2008

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

Por 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
Publicado em 2003

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

Por 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.
Publicado em 2000

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

Por 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 
Publicado em 2006

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

Por 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
Publicado em 2008

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

Por 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
Publicado em 2008