MP:0000219 | increased neutrophil count | "greater than normal neutrophil numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002463 | abnormal neutrophil physiology | "abnormal function of these granular leukocytes, which stain with neutral dyes" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002941 | increased circulating alanine transaminase level | "increased concentration in the blood of this enzyme, which transfers amino groups from l-alanine to 2 ketoglutarate, or the reverse (from l-glutamate to pyruvate); serum concentration is increased in viral hepatitis and myocardial infarction" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002944 | increased lactate dehydrogenase level | "greater than the normal concentration of this enzyme, which catalyzes the interconversion of lactate and pyruvate" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:87714] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003628 | abnormal lymphocyte adhesion | "anomaly in the number of or process by which lymphocytes adhere to the luminal aspects of high endothelial venules prior to transmigration out of the vessel" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:95656] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003888 | liver hemorrhage | "bleeding within the liver" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0005565 | increased blood urea nitrogen level | "high circulating concentration of nitrogen, in the form of urea; commonly used to measure renal function" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0008735 | increased susceptibility to endotoxin shock | "more than the expected early reaction of the microcirculation to endotoxins such as LPS, characterized by movement of fluid and leukocytes from the blood into extravascular tissues and often resulting in death" [MGI:tmeehan "Terry Meehan, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0009788 | increased susceptibility to bacterial infection induced morbidity/mortality | "increased likelihood that an organism will display the expected moribund state caused by a bacterial invasion or from components of or toxins produced by bacteria" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0010080 | abnormal hepatocyte physiology | "any functional anomaly of the main structural specialized epithelial cells which normally organize into interconnected plates called lobules" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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MP:0012246 | abnormal hepatic cord morphology | "any structural anomaly of the three-dimensional arrangement formed by plates of hepatocytes, usually one cell thick, that radiates from the center of the liver lobule; hepatic laminae are highly branched, irregular structures bordered by endothelial lined vascular spaces called hepatic sinusoids" [MGI:anna] |
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Allelic Composition: Pknox1tm2.1Fbla/Pknox1tm2.1Fbla,Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd
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