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Phenotypes developed in secretin receptor-null mice indicated a role for secretin in regulating renal water reabsorptionAn allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.Automated video analysis system reveals distinct diurnal behaviors in C57BL/6 and C3H/HeN mice.Congenic mice confirm that collagen X is required for proper hematopoietic development.The Interaction of Genetic Background and Mutational Effects in Regulation of Mouse Craniofacial Shape.Allelic Variation in the Toll-Like Receptor Adaptor Protein Ticam2 Contributes to SARS-Coronavirus Pathogenesis in Mice.Mouse genetic background influences the dental phenotype.Parallel universes of Black Six biology.Progressive renal papillary calcification and ureteral stone formation in mice deficient for Tamm-Horsfall proteinRNAi phenotypes are influenced by the genetic background of the injected strain.The relevance of individual genetic background and its role in animal models of epilepsyHigh-Speed Mouse Backcrossing Through the Female Germ Line.miRNA-mediated risk for schizophrenia in 22q11.2 deletion syndrome.Ethanol drinking in rodents: is free-choice drinking related to the reinforcing effects of ethanol?Strain-specific spontaneous and NNK-mediated tumorigenesis in Pten+/- miceAntioxidant role of glutathione S-transferases: 4-Hydroxynonenal, a key molecule in stress-mediated signalingThe many faces of nitric oxide: cytotoxic, cytoprotective or both.The role of caveolin-1 in pulmonary matrix remodeling and mechanical properties.Meprin A metalloproteases enhance renal damage and bladder inflammation after LPS challenge.Airway and lung pathology due to mucosal surface dehydration in {beta}-epithelial Na+ channel-overexpressing mice: role of TNF-{alpha} and IL-4R{alpha} signaling, influence of neonatal development, and limited efficacy of glucocorticoid treatmentPlacental insufficiency associated with loss of Cited1 causes renal medullary dysplasiaSpontaneous vulvar papillomas in a colony of mice used for pancreatic cancer research.Generation of a C57BL/6 MYC-Driven Mouse Model and Cell Line of Prostate Cancer.Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line.A major QTL on mouse chromosome 17 resulting in lifespan variability in SOD1-G93A transgenic mouse models of amyotrophic lateral sclerosis.Depletion of annexin A5, annexin A6, and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 response.Embryonic lethality and defective male germ cell development in mice lacking UTF1.Relaxin-3 null mutation mice display a circadian hypoactivity phenotype.Mouse strain determines the outcome of wound healing after myocardial infarction.General strategy to analyse coat colour phenotypes in mice.The impact of genetic background and Bid on the phenotype of Bcl-2-deficiency in mice.Insights into the pathogenesis of herpes simplex encephalitis from mouse models
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Genetic variables that influence phenotype.
@ast
Genetic variables that influence phenotype.
@en
type
label
Genetic variables that influence phenotype.
@ast
Genetic variables that influence phenotype.
@en
prefLabel
Genetic variables that influence phenotype.
@ast
Genetic variables that influence phenotype.
@en
P2860
P356
P1433
P1476
Genetic variables that influence phenotype.
@en
P2093
Carol Cutler Linder
P2860
P304
P356
10.1093/ILAR.47.2.132
P577
2006-01-01T00:00:00Z