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Journal of Neurobiology
|
January 20, 2000
Partial rescue of the ocular retardation phenotype by genetic modifiers
C Bone-Larson, S Basu, J D Radel, et al.
Artificial Life
|
May 12, 2001
Open problems in artificial life
M A Bedau, J S McCaskill, N H Packard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss
P A Sieving, M L Fowler, R A Bush, et al.
Genomics
|
September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus
S A Keller, J M Jones, A Boyle, et al.
Molecular Genetics and Metabolism
|
March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants
D A Pillers, R G Weleber, D G Green, et al.
Page
of 9
Search research articles
Search
Showing results (81-90 of 85) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 85 results.
Journal of Neurobiology
|
January 20, 2000
Partial rescue of the ocular retardation phenotype by genetic modifiers
C Bone-Larson, S Basu, J D Radel, et al.
Artificial Life
|
May 12, 2001
Open problems in artificial life
M A Bedau, J S McCaskill, N H Packard, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 24, 2001
Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss
P A Sieving, M L Fowler, R A Bush, et al.
Genomics
|
September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus
S A Keller, J M Jones, A Boyle, et al.
Molecular Genetics and Metabolism
|
March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants
D A Pillers, R G Weleber, D G Green, et al.
Page
of 9