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

بواسطة Roderick, Thomas H., Hawes, Norman L.
منشور في 1970

Nineteen Paracentric Chromosomal Inversions in Mice

بواسطة Roderick, Thomas H., Hawes, Norman L.
منشور في 1974

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

بواسطة Kiernan, Amy E., Li, Renhua, Hawes, Norman L., Churchill, Gary A., Gridley, Thomas
منشور في 2007

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

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

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation

بواسطة Anderson, Michael G., Hawes, Norman L., Trantow, Colleen M., Chang, Bo, John, Simon W.M.
منشور في 2007

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

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

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

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

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

بواسطة 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
منشور في 2001

Restoration of cone vision in a mouse model of achromatopsia

بواسطة 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
منشور في 2007

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

بواسطة 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.
منشور في 2002

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

بواسطة 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
منشور في 2001

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

بواسطة 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.
منشور في 2008

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

بواسطة 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
منشور في 2003

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

بواسطة 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.
منشور في 2000

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

بواسطة 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 
منشور في 2006

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

بواسطة 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
منشور في 2008

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

بواسطة 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
منشور في 2008