Authors:
Smith, RS
Hawes, NL
Chang, B
Roderick, TH
Akeson, EC
Heckenlively, JR
Gong, XH
Wang, X
Davisson, MT
Citation: Rs. Smith et al., Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract, GENOMICS, 63(3), 2000, pp. 314-320
Authors:
Hawes, NL
Chang, B
Hageman, GS
Nusinowitz, S
Nishina, PM
Schneider, BS
Smith, RS
Roderick, TH
Davisson, MT
Heckenlively, JR
Citation: Nl. Hawes et al., Retinal degeneration 6 (rd6): A new mouse model for human retinitis punctata albescens, INV OPHTH V, 41(10), 2000, pp. 3149-3157
Authors:
Akhmedov, NB
Piriev, NI
Chang, B
Rapoport, AL
Hawes, NL
Nishina, PM
Nusinowitz, S
Heckenlively, JR
Roderick, TH
Kozak, CA
Danciger, M
Davisson, MT
Farber, DB
Citation: Nb. Akhmedov et al., A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse, P NAS US, 97(10), 2000, pp. 5551-5556
Authors:
Klebanov, S
Flurkey, K
Roderick, TH
Archer, JR
Astle, MC
Chen, J
Harrison, DE
Citation: S. Klebanov et al., Heritability of life span in mice and its implication for direct and indirect selection for longevity, GENETICA, 110(3), 2000, pp. 209-218
Authors:
Chang, B
Hawes, NL
Roderick, TH
Smith, RS
Heckenlively, JR
Horwitz, J
Davisson, MT
Citation: B. Chang et al., Identification of a missense mutation in the alpha A-crystallin gene of the lop18 mouse, MOL VIS, 5(21), 1999, pp. NIL_1-NIL_5