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

Autor Roderick, Thomas H., Hawes, Norman L.
Vydáno 1970

Nineteen Paracentric Chromosomal Inversions in Mice

Autor Roderick, Thomas H., Hawes, Norman L.
Vydáno 1974

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

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

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

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

Iris phenotypes and pigment dispersion caused by genes influencing pigmentation

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

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

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

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

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

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

Autor 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
Vydáno 2001

Restoration of cone vision in a mouse model of achromatopsia

Autor 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
Vydáno 2007

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

Autor 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.
Vydáno 2002

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

Autor 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
Vydáno 2001

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

Autor 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.
Vydáno 2008

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

Autor 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
Vydáno 2003

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

Autor 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.
Vydáno 2000

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

Autor 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 
Vydáno 2006

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

Autor 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
Vydáno 2008

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

Autor 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
Vydáno 2008