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corneal opacity/phosphatase
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Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l) gene.
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BACKGROUND
Waved with open eyelids 2 (woe2) is a novel autosomal recessive mouse mutation that arose spontaneously in our animal facility. Upon initial evaluation, mutant mice exhibited eyelids open at birth (EOB) and wavy fur phenotypes. The goals of this study were to phenotypically characterize
Molecular prevalence and haemato-biochemical profile of canine monocytic ehrlichiosis in dogs in and around Hisar, Haryana, India.
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The present study was planned to investigate the molecular prevalence of canine monocytic ehrlichiosis (CME) in dogs in and around Hisar and to evaluate the haemato-biochemical profile for its better management. A total of 60 dogs presented to Medicine Section, TVCC, LUVAS, Hisar with the history of
Hypophosphatasia: Novel Mutation Associated With An Atypical Newborn Presentation
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<p>Hypophosphatasia, a rare genetic disease affecting bone metabolism, is characterized by decreased activity of tissue nonspecificalkaline phosphatase (TNAP). The gene encoding TNSP (ALPL) has considerable allelic heterogeneity, which couldexplain different degrees of enzyme activity
Characterization of serum lysosomal enzymatic activities. II. Effect of lumpy skin disease in Egyptian cows.
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Clinical findings and lysosomal enzymes (LYE) in eight lumpy skin diseases (LSD) cows and same number of healthy ones were reported in Tal-El Baker village and Tal Alkabir centre, Ismailia province, Egypt. LSD began with fever, anorexia, skin lesions in form of nodules all over the body, which
Spontaneous hypoparathyroidism: clinical, biochemical and radiological features.
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The clinical, biochemical and radiological features of spontaneously occurring hypoparathyroidism in 13 patients (mean age 9 years, range 4 months to 20 years) are highlighted. Nine patients presented with a history of generalised seizures and 2 were in acute hypocalcemic crisis at the time of
LCAT protects against Lipoprotein-X formation in a murine model of drug-induced intrahepatic cholestasis.
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Familial lecithin:cholesterol acyltransferase (LCAT) deficiency (FLD) is a rare genetic disease characterized by low HDL-C levels, low plasma cholesterol esterification, and the formation of Lipoprotein-X (Lp-X), an abnormal cholesterol-rich lipoprotein particle. LCAT deficiency causes corneal
The mucosal toxicity of different benzalkonium chloride analogues evaluated with an alternative test using slugs.
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OBJECTIVE
The objective of this study was to evaluate the mucosal toxicity of different benzalkonium chloride (BAC) analogues using slugs as the alternative test organism.
METHODS
The effect of different BAC analogues on the mucosal tissue of slugs was determined from the protein, lactate
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