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Find link is a tool written by Edward Betts.Longer titles found: Factor VIII (medication) (view)
searching for Factor VIII 72 found (234 total)
alternate case: factor VIII
LMAN1
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identified as the disease gene leading to combined deficiency of factor V-factor VIII, a rare, autosomal recessive disorder in which both coagulation factorsMCFD2 (670 words) [view diff] exact match in snippet view article find links to article
gene. Mutations in MCFD2 cause the combined deficiency of factor V and factor VIII (F5F8D), a recessive bleeding disorder. MCFD2 and ERGIC-53 (or LMAN1)Proteins produced and secreted by the liver (485 words) [view diff] exact match in snippet view article find links to article
coagulation cascade. While the endothelium does produce some factor VIII, the majority of factor VIII is produced in the liver. Inhibitors of coagulation: InactivateFrances Rotblat (557 words) [view diff] exact match in snippet view article find links to article
Rodriguez; D. P. O'Brien; Frances Rotblat; et al. (1984). "Structure of human factor VIII". Nature. 312 (5992): 337–342. Bibcode:1984Natur.312..337V. doi:10.1038/312337a0Biotechnology in pharmaceutical manufacturing (1,528 words) [view diff] exact match in snippet view article find links to article
that 60 to 80 percent of patients with hemophilia who were exposed to factor VIII concentrates between 1979 and 1984 are seropositive for HIV by [the]Factor XII deficiency (713 words) [view diff] exact match in snippet view article find links to article
disorders, specifically the hemophilias: hemophilia A with a deficiency in factor VIII or antihemophilic globulin, hemophilia B with a deficiency in factorBleeding diathesis (809 words) [view diff] exact match in snippet view article find links to article
inhibitors of coagulation. The main inhibitor is directed against clotting factor VIII. Another example is antiphospholipid syndrome, an autoimmune, hypercoagulableTRA (gene) (993 words) [view diff] exact match in snippet view article
"Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene". Hum. Mol. Genet. 1 (3): 179–86. doi:10.1093/hmg/1.3.179. PMID 1303175Thrombodynamics test (663 words) [view diff] exact match in snippet view article find links to article
Ovanesov M.V.; Lopatina E.G.; Saenko E.L.; et al. (2003). "Effect of factor VIII on tissue factor-initiated spatial clot growth". Thromb Haemost. 89 (2):Armour and Company (1,657 words) [view diff] exact match in snippet view article find links to article
assets of Armour Pharmaceuticals are now part of CSL Behring. Armour's Factor VIII product "Factorate" was widely reported as infecting thousands of hemophiliacsDextran (1,402 words) [view diff] exact match in snippet view article find links to article
erythrocyte aggregation and platelet adhesiveness. Dextrans also reduce factor VIII-Ag Von Willebrand factor, thereby decreasing platelet function. ClotsWeibel–Palade body (1,558 words) [view diff] exact match in snippet view article find links to article
important in secondary hemostasis, acting as a chaperone for coagulation factor VIII (FVIII). Endothelial activation Standring, S (2016). Gray's anatomy :List of histologic stains that aid in diagnosis of cutaneous conditions (254 words) [view diff] exact match in snippet view article find links to article
adnexal carcinoma Sebaceous carcinoma Renal cell carcinoma Schwannoma Factor VIII Dabska-type hemangioendothelioma Angiosarcoma Factor XIII Cutaneous focalBispecific monoclonal antibody (3,551 words) [view diff] exact match in snippet view article find links to article
(October 2012). "A bispecific antibody to factors IXa and X restores factor VIII hemostatic activity in a hemophilia A model". Nature Medicine. 18 (10):Gliosarcoma (1,592 words) [view diff] exact match in snippet view article find links to article
Jones TR, Pizzo SV, Bigner DD (1982) Immunohistochemical detection of factor VIII/von Willebrand factor in hyperplastic endothelial cells in glioblastomaJuvenile dermatomyositis (1,139 words) [view diff] exact match in snippet view article find links to article
include myositis-specific or -related antibodies, nailfold capillaroscopy, factor VIII-related antigen, muscle ultrasound, calcinosis and neopterin. Once aDominique Meyer (biologist) (999 words) [view diff] exact match in snippet view article
(1976) 262, 141–142 Zimmerman T.S., Abildgaard C.F., Meyer D. The factor VIII abnormality in severe von Willebrand's disease. N. Engl. J. Med. (1979)Arthur Bloom (physician) (938 words) [view diff] exact match in snippet view article
that Bloom had knowingly downplayed the risks of contracting HIV from Factor VIII blood products. In the following year the allegation was repeated inHelge Stormorken (2,076 words) [view diff] exact match in snippet view article find links to article
females with concomitant von Willebrand's disease and carriership for factor VIII". Thrombosis Research. 28 (1): 133–6. doi:10.1016/0049-3848(82)90041-XFitusiran (714 words) [view diff] exact match in snippet view article find links to article
of age and older with hemophilia A or hemophilia B, with or without factor VIII or IX inhibitors (neutralizing antibodies). The US Food and Drug AdministrationBRCC3 (968 words) [view diff] exact match in snippet view article find links to article
"Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene". Human Molecular Genetics. 1 (3): 179–86. doi:10.1093/hmg/1.3.179Lower gastrointestinal bleeding (2,048 words) [view diff] exact match in snippet view article find links to article
VII has been approved for use in patients with hemophilia A and B with factor VIII and IX inhibitors. Evidence of possible benefit in patients with cirrhosisVasopressin receptor (974 words) [view diff] exact match in snippet view article find links to article
cell insertion of AQP-2 water channels into apical membrane, induction of AQP-2 synthesis, releases von Willebrand factor and factor VIII, vasodilationStructural variation (3,555 words) [view diff] exact match in snippet view article find links to article
related to human disease. For instance, recurrent 400kb inversion in factor VIII gene is a common cause of haemophilia A, and smaller inversions affectingFresh frozen plasma (1,792 words) [view diff] exact match in snippet view article find links to article
when fibrinogen is needed. For treatment of hemophilia A, recombinant factor VIII concentrates are available. For treatment of severe hemophilia B, recombinantGenetics Institute (434 words) [view diff] exact match in snippet view article find links to article
morphogenetic protein 2,recombinant human Factor IX, and recombinant human Factor VIII (Recombinate); as well as tissue plasminogen activator and erythropoetinList of diseases (F) (925 words) [view diff] exact match in snippet view article
deficiency Factor V deficiency Factor V Leiden mutation Factor VII deficiency Factor VIII deficiency Factor X deficiency, congenital Factor X deficiency FactorX chromosome (3,997 words) [view diff] exact match in snippet view article find links to article
assembly checkpoint helicase FAAH2: Fatty acid amide hydrolase 2 F8A1: Factor VIII intron 22 protein FAM104B: encoding protein Family with sequence similaritySwedish Orphan Biovitrum (814 words) [view diff] exact match in snippet view article find links to article
following year to also include the development of a long-lasting recombinant factor VIII Fc fusion protein candidate, rFVIIIFc, for the treatment of hemophiliaList of diseases (A) (1,972 words) [view diff] exact match in snippet view article
insufficiency, familial Anterograde amnesia Anthrax Anti amnestic syndrome Anti-factor VIII autoimmunization Antigen-peptide-transporter 2 deficiency Anti-HLA hyperimmunizationMads Melbye (2,230 words) [view diff] exact match in snippet view article find links to article
same year that HIV infection was caused by commercially manufactured factor VIII based on blood from American donors. The paper was accompanied by anLentiviral vector in gene therapy (3,420 words) [view diff] exact match in snippet view article find links to article
targets the haematopoietic cells in order to increase the amount of factor VIII, which is affected in haemophilia A. But this continues to be a subjectHLF (gene) (927 words) [view diff] exact match in snippet view article
heterodimers represents one mechanism of PAR protein transactivation of the factor VIII and factor IX genes". DNA and Cell Biology. 18 (2): 165–73. doi:10.1089/104454999315556Affibody molecule (2,405 words) [view diff] exact match in snippet view article find links to article
M; Kelley, B; Ljungqvist, C; Nygren, P-A (2001). "Recombinant human factor VIII-specific affinity ligands selected from phage-displayed combinatorialNeurodegenerative disease (6,966 words) [view diff] exact match in snippet view article find links to article
Evaluation and (12 April 2019). "Variant Creutzfeldt-Jakob Disease (vCJD) and Factor VIII (pdFVIII) Questions and Answers". FDA. Retrieved 31 March 2022. Lin MTOPN1LW (2,416 words) [view diff] exact match in snippet view article find links to article
the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region". Genomics. 4 (4): 460–71. doi:10DBP (gene) (1,353 words) [view diff] exact match in snippet view article
heterodimers represents one mechanism of PAR protein transactivation of the factor VIII and factor IX genes". DNA and Cell Biology. 18 (2): 165–173. doi:10ADAMDEC1 (415 words) [view diff] exact match in snippet view article find links to article
Schambeck, C. M. (2008). "Association of ADAMDEC1 haplotype with high factor VIII levels in venous thromboembolism". Thrombosis and Haemostasis. 99 (5):H2AFB1 (500 words) [view diff] exact match in snippet view article find links to article
PMID 15257289. Naylor JA, Buck D, Green P, et al. (1995). "Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions"PEGylation (3,006 words) [view diff] exact match in snippet view article find links to article
the FDA for the US in May 2018. Adynovate – PEGylated Antihemophilic Factor VIII for the treatment of patients with hemophilia A. (Baxalta, 2015) IrinotecanH2AFB2 (385 words) [view diff] exact match in snippet view article find links to article
PMID 15257289. Naylor JA, Buck D, Green P, et al. (1995). "Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions"National Institute for Health and Care Research (4,437 words) [view diff] exact match in snippet view article find links to article
Pierce, Glenn F.; Wong, Wing Y.; Pasi, K. John (28 December 2017). "AAV5–Factor VIII Gene Transfer in Severe Hemophilia A". New England Journal of MedicineFibronectin (3,397 words) [view diff] no match in snippet view article find links to article
1111/1523-1747.ep12525694. PMID 7240787. Bruhn HD, Heimburger N (1976). "Factor-VIII-related antigen and cold-insoluble globulin in leukemias and carcinomas"Charles Rizza (315 words) [view diff] exact match in snippet view article find links to article
his thesis Conditions affecting the level of antihaemophilic globulin (factor VIII) in the blood. Between 1958 and 1961, Rizza held the post of MedicalJay A. Levy (950 words) [view diff] exact match in snippet view article find links to article
wet and dry heat procedures of AIDS-associated retrovirus (ARV) during factor VIII purification from plasma". The Lancet. 325 (8443): 1456–1457. doi:10VLDL receptor (4,736 words) [view diff] exact match in snippet view article find links to article
low-density lipoprotein receptor-related protein are shared within coagulation factor VIII". Blood Coagul. Fibrinolysis. 19 (2): 166–77. doi:10.1097/MBC.0b013e3282f5457bMFGE8 (1,285 words) [view diff] exact match in snippet view article find links to article
globule protein that is highly expressed in human breast tumors contains factor VIII-like domains". Cancer Res. 51 (18): 4994–8. PMID 1909932. Maruyama KFranz König (surgeon) (447 words) [view diff] exact match in snippet view article
3316236. PMID 3316236. Archived from the original (PDF) on 2009-03-18. Factor VIII - von Willebrand Factor, Volume 1 by M. J. Seghatchian, G. F. SavidgeMPP1 (800 words) [view diff] exact match in snippet view article find links to article
erythrocyte membrane protein, p55, originates at the CpG island 3' to the factor VIII gene". Hum. Mol. Genet. 1 (2): 97–101. doi:10.1093/hmg/1.2.97. PMID 1301163Bio Products Laboratory (1,251 words) [view diff] exact match in snippet view article find links to article
established. During the 1970s and early 1980s it became apparent that Factor VIII products produced at the BPL site (and other products from other companies)MTCP1 (1,126 words) [view diff] exact match in snippet view article find links to article
"Isolation and sequence of two genes associated with a CpG island 5' of the factor VIII gene". Hum. Mol. Genet. 1 (3): 179–86. doi:10.1093/hmg/1.3.179. PMID 1303175Grand Duchess Tatiana Nikolaevna of Russia (8,051 words) [view diff] exact match in snippet view article find links to article
Imperial Family. The Glorification of the Royal Family Hemophilia A (Factor VIII Deficiency) Coble, Michael D.; Loreille, Odile M.; et al. (11 March 2009)H2AFB3 (580 words) [view diff] exact match in snippet view article find links to article
Williamson H, Bentley D, Giannelli F (July 1995). "Investigation of the factor VIII intron 22 repeated region (int22h) and the associated inversion junctions"List of diseases (M) (2,470 words) [view diff] exact match in snippet view article
pterygium syndrome Multiple s – Multiple v Multiple sclerosis ichthyosis factor VIII deficiency Multiple sclerosis Multiple subcutaneous angiolipomas MultipleGrand Duchess Olga Nikolaevna of Russia (9,246 words) [view diff] exact match in snippet view article find links to article
alexanderpalace.org FrozenTears.org A media library of the last Imperial Family. Hemophilia A (Factor VIII Deficiency) The Glorification of the Royal FamilyMisconceptions about HIV/AIDS (7,533 words) [view diff] exact match in snippet view article find links to article
Study investigators found that neither the purity nor the amount of factor VIII therapy had a deleterious effect on CD4+ T-cell counts. Similarly, theChristopher Statton (1,046 words) [view diff] exact match in snippet view article find links to article
eighties by the pharmaceutical companies that were producing concentrate factor VIII, namely the Bayer Corporation. Living with these diseases for all orBob Massie (activist) (2,434 words) [view diff] exact match in snippet view article
Gorbachev. Massie was born with severe classical hemophilia, also known as "Factor VIII hemophilia", a genetic disease that prevents the blood from clottingHaig Kazazian (2,370 words) [view diff] exact match in snippet view article find links to article
J.D.; Kazazian, H.H. (May 1995). "Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A". Nature Genetics. 10 (1): 119–121Henri Termeer (3,843 words) [view diff] exact match in snippet view article find links to article
Therapeutics division of Baxter Travenol in Glendale, California. Hyland sold Factor VIII, Factor IX, immunoglobulins, and albumin. The plasma was collected throughSex differences in human physiology (12,597 words) [view diff] exact match in snippet view article find links to article
recessive disorders include: Red-green colour blindness Haemophilia A (factor VIII) Haemophilia B (factor IX) Duchenne Muscular Dystrophy X-linked agammaglobulinaemiaCaerphilly Heart Disease Study (3,775 words) [view diff] exact match in snippet view article find links to article
Rumley A, Lowe GD, Sweetnam PM, Yarnell JW, Ford RP (April 1999). "Factor VIII, von Willebrand factor and the risk of major ischaemic heart diseaseFereydoun Ala (1,825 words) [view diff] exact match in snippet view article find links to article
time, was frozen fresh plasma and the newly discovered cryoprecipitated Factor VIII concentrate (Judith Pool in 1967), as industrial concentrates were notRegulatory macrophages (1,836 words) [view diff] exact match in snippet view article find links to article
Henry KL, Dumont J, Peters RT, et al. (November 2018). "Recombinant factor VIII Fc fusion protein drives regulatory macrophage polarization". Blood AdvancesANNOVAR (3,454 words) [view diff] exact match in snippet view article find links to article
Stylianos E.; Gitschier, Jane (November 1993). "Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A". Nature Genetics. 5No-SCAR genome editing (5,654 words) [view diff] exact match in snippet view article find links to article
Dong-Wook; Kim, Jin-Soo (2015-08-06). "Functional Correction of Large Factor VIII Gene Chromosomal Inversions in Hemophilia A Patient-Derived iPSCs UsingAdvisory Committee on the Virological Safety of Blood (2,323 words) [view diff] exact match in snippet view article find links to article
for 72 hours reduced but did not always eliminate detectable B19 from factor VIII concentrates, consistent with recent observations that current methodsEllinor Peerschke (1,953 words) [view diff] exact match in snippet view article find links to article
Ledford-Kraemer M, Van Cott EM, Meijer P (April 2009). "Laboratory assessment of factor VIII inhibitor titer: the North American Specialized Coagulation LaboratoryHIV Haemophilia Litigation (4,248 words) [view diff] exact match in snippet view article find links to article
National Health Service Act of 1977 and in negligence over HIV-contaminated factor VIII concentrate imported into the UK from the USA. "HIV Haemophiliac LitigationStructural variation in the human genome (3,756 words) [view diff] exact match in snippet view article find links to article
Antonarakis, S.E.; Gitschier, J. (1993). "Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A". Nat. Genet. 5 (3):Fariba Naderi (1,666 words) [view diff] exact match in snippet view article find links to article
role 2009 Non-Confidential Masoud Rasam IRIB TV5 TV series; main role Factor VIII Mina Iranmanesh Reza Karimi IRIB TV1 TV series; supporting role 2010List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article
301500; GLA Fabry disease, cardiac variant; 301500; GLA Factor V and factor VIII, combined deficiency of; 227300; MCFD2 Factor V deficiency; 227400; F5