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1,696 Possible Causes for Hemochromatosis, mouse, protein

Did you mean: Hemochromatosis, morus, proteus

  • Neuroferritinopathy

    In order to analyze the impact of the mutation in vivo, we generated mouse models for the some pathogenic human FTL gene in FVB and C57BL/6J strains.[ncbi.nlm.nih.gov] HEMOCHROMATOSIS I.[faculty.washington.edu] Abstract Ferritin is the main intracellular protein of iron storage with a central role in the regulation of iron metabolism and detoxification.[ncbi.nlm.nih.gov]

  • Echovirus Infection

    Abstract Mouse cells are not susceptible to infection with echovirus 1 (EV-1) because they lack the viral receptor, human VLA-2.[ncbi.nlm.nih.gov] Abnormal Bile Acid Metabolism and Neonatal Hemochromatosis: A Subset with Poor Prognosis. J Pediatr Gastroenterol Nutr. 1997;25(3):321-6.[ama.ba] Polarized sorting of GPI-linked proteins in epithelia and membrane microdomains. Cell Biology International Reports 15, 1023 -1049.[jgv.microbiologyresearch.org]

  • Aplastic Anemia

    […] investigate the effects of DGBX on the regulation of the balance between proliferation and apoptosis of hematopoietic stem cells (HSCs) due to the aberrant immune response in a mouse[ncbi.nlm.nih.gov] Although hemochromatosis is a comparatively rare condition, its association with aplastic anemia is frequent enough to suggest that the combination of the two diseases is[jamanetwork.com] […] of the transcription factor C/EBP homologous protein.[ncbi.nlm.nih.gov]

  • Exchange Transfusion

    The performance of HbVs as a substitute for RBC transfusions was examined in a mouse model of pneumonectomy following acute 40% exchange-transfusion with HbVs.[ncbi.nlm.nih.gov] Here we describe two siblings affected by neonatal hemochromatosis.[ncbi.nlm.nih.gov] Protein electrophoresis and immunofixation of the infant girl's serum and urine samples showed the presence of a paraprotein electrophoretically identical to that found in[ncbi.nlm.nih.gov]

  • Diamond-Blackfan Anemia

    Conversely, Rps7 mouse mutants show no anemia or hyperpigmentation, phenotypes associated with mutation of human RPS7 and other murine RPs, respectively.[ncbi.nlm.nih.gov] PATIENT AND METHODS: A case is presented of a 5-year-old girl who had transfusion-dependent Diamond-Blackfan anemia and hemochromatosis and who developed an osteogenic sarcoma[ncbi.nlm.nih.gov] , along with rarer abnormalities of additional ribosomal proteins.[ncbi.nlm.nih.gov]

  • Fissured Tongue

    Species Human, Mouse Applications WB, ICC/IF, IHC H00002316-M01 Mouse Monoclonal Species Human Applications WB, ELISA, IHC-P Alternate Names Fissured Tongue is also known[novusbio.com] Interactions unavailable Genome Viewer unavailable Damaging Variants unavailble for Mouse Damaging Variants unavailable Protein-Protein Interactions Genome Viewer Damaging[rgd.mcw.edu] No differences between the groups existed in the amounts of salivary potassium, calcium, inorganic phosphate, amylase and total protein.[ncbi.nlm.nih.gov]

  • Valacyclovir

    Here, we developed and validated a simple, sensitive and robust LC-MS/MS method for measuring the prodrug valacyclovir (VACV) and its metabolite acyclovir (ACV) in mouse and[ncbi.nlm.nih.gov] Trending Stories Scientists discover new blood vessels in bone Unplanned C-sections put new mothers at greater risk of developing postnatal depression Study shows hereditary hemochromatosis[news-medical.net] Abstract Homocysteinylation of lysine residues by homocysteine thiolactone (HCTL), a reactive homocysteine metabolite, results in protein aggregation and malfunction, and[ncbi.nlm.nih.gov]

  • Vibrio Cholerae

    In this study, we have generated biofilm-altered Tn5 mutants of V. cholerae O139 and evaluated their in vivo colonization ability on mouse model.[ncbi.nlm.nih.gov] Abstract We report a case of bacteremia associated with hemorrhagic bullous skin lesions on the leg caused by non-01, non-0139 Vibrio cholerae in a 66-year-old man with hemochromatosis[ncbi.nlm.nih.gov] Also, SlmA is a member of the TetR family of proteins, which are generally transcriptional repressors.[ncbi.nlm.nih.gov]

  • Erythrocytosis

    Studies employing genetically modified mice point to Hif-2α, one of two main Hif-α isoforms, as being the critical regulator of Epo in the adult mouse.[ncbi.nlm.nih.gov] SS disease, SS trait (no sickle cells on smear) hemolytic anemia unbalanced synthesis of alpha and beta chains of hemoglobin - clinical problem: iron overload (secondary hemochromatosis[quizlet.com] proteins.[ncbi.nlm.nih.gov]

  • Phenobarbital

    The CYP2B6-humanized mouse will be valuable for studies on in vivo roles of hepatic CYP2B6 in xenobiotic metabolism and toxicity.[ncbi.nlm.nih.gov] Further investigation revealed that she had hereditary hemochromatosis due to homozygosity for H63D HFE gene.[bloodjournal.org] Of these two therapies, hemoperfusion is generally considered to be more effective because phenobarbital shows significant protein binding.[ncbi.nlm.nih.gov]

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