Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M T Davisson"'
Publikováno v:
Human Reproduction. 22:468-476
Background Chromosomal abnormalities frequently are associated with impairment or arrest of spermatogenesis in mammals but are compatible with fertility in female carriers of the same anomaly. In the case of trisomy, mice have extra genomic DNA as we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad63e172696c1e7f35b6db7ee9d7cee1
https://doi.org/10.1093/humrep/del397
https://doi.org/10.1093/humrep/del397
Autor:
M T Davisson, K R Johnson
Publikováno v:
Mammalian Genome. 4:S253-S260
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51530a7d682380d1494472bee2adc684
https://doi.org/10.1007/bf00360844
https://doi.org/10.1007/bf00360844
Publikováno v:
Neural networks : the official journal of the International Neural Network Society. 11(4)
This paper provides the results of our study on automatic classification of mouse chromosomes. A radial basis function neural network was compared with a multi-layer perceptron and a probabilistic neural network. The networks were trained and tested
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b06b19878dc0f3b38b5d3b913c6d8e
https://pubmed.ncbi.nlm.nih.gov/12662815
https://pubmed.ncbi.nlm.nih.gov/12662815
Publikováno v:
ICNN
This paper presents the results of our experiments for classification of mouse chromosomes using a radial basis function (RBF) and a probabilistic neural network (PNN). The fast orthogonal search (FOS) was utilized for training of the RBF network. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86468810ffdcfecc127b557f33e20176
https://doi.org/10.1109/icnn.1996.549008
https://doi.org/10.1109/icnn.1996.549008
Publikováno v:
Physiologybehavior. 73(5)
Genetically engineered strains of mice, modified by transgenesis or gene targeting ("knockouts") are being generated at an impressive rate and used, among other areas, as premiere research tools in deciphering the genetic basis of behavior. As behavi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60da0a6085e7467efda668ae181b90c5
https://pubmed.ncbi.nlm.nih.gov/11566202
https://pubmed.ncbi.nlm.nih.gov/11566202
Publikováno v:
Lab animal. 29(3)
The Mouse Genome Database supports the use of mice in genome research, offering researchers information on gene characterization, genetic maps, comparative genomic data, and phenotypes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd66e70a290aca8091932bda90d96acc
https://pubmed.ncbi.nlm.nih.gov/11375645
https://pubmed.ncbi.nlm.nih.gov/11375645
Autor:
N L, Hawes, B, Chang, G S, Hageman, S, Nusinowitz, P M, Nishina, B S, Schneider, R S, Smith, T H, Roderick, M T, Davisson, J R, Heckenlively
Publikováno v:
Investigative ophthalmologyvisual science. 41(10)
To characterize the genetics and phenotype of a new mouse mutant with retinal degeneration, rd6, that is associated with extensive, scattered, small white retinal dots seen ophthalmoscopically.The phenotype was characterized using ophthalmoscopy, fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::471698085d4b73d0ba8dd84d8f0e4055
https://pubmed.ncbi.nlm.nih.gov/10967077
https://pubmed.ncbi.nlm.nih.gov/10967077
Publikováno v:
Nucleic acids research. 28(1)
The Mouse Genome Database (MGD) is a comprehensive public database of mouse genomic, genetic and phenotypic information (http://www.informatics.jax.org ). This community database provides information about genes, serves as a mapping resource of the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::38000029f6cfd478cac5f0492afa6012
https://pubmed.ncbi.nlm.nih.gov/10592195
https://pubmed.ncbi.nlm.nih.gov/10592195
Autor:
B, Chang, N L, Hawes, T H, Roderick, R S, Smith, J R, Heckenlively, J, Horwitz, M T, Davisson
Publikováno v:
Molecular vision. 5
The mouse lop18 (lens opacity 18) mutation causes a white cataract obvious at weaning age. It soon progresses to a large white nuclear cataract with mild cortical changes. The mutation maps to mouse Chromosome 17 in close linkage to the alphaA-crysta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9acfef6e4dc5100fd6e114073367156
https://pubmed.ncbi.nlm.nih.gov/10493778
https://pubmed.ncbi.nlm.nih.gov/10493778
Publikováno v:
The Journal of heredity. 89(6)
A new allelic series at the underwhite gene is described. Three of the alleles in the series--uw, uwd, and Uwdbr--arose as spontaneous mutations on different genetic backgrounds at The Jackson Laboratory. We report here the visible phenotypes and dom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::189b0c086e64a8a2f804634f8d92b1df
https://pubmed.ncbi.nlm.nih.gov/9864865
https://pubmed.ncbi.nlm.nih.gov/9864865