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BioGlobe

www.pharmacologicum-hamburg.de/

BioGlobe, Molecular Genetic Laboratory, leader in the field of molecular diagnostics

Pharmacologicum-hamburg.de

Pharmacologicum-hamburg.de is hosted in Germany . Pharmacologicum-hamburg.de doesn't use HTTPS protocol. Number of used technologies: 2. First technologies: CSS, Html, Number of used javascripts: 0. Number of used analytics tools: 0. Its server type is: Apache.

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Name: Keywords
Content: 11-beta-Cortisol-Ketoreduktase-Defizienz, 11-b-Hydroxysteroid-Dehydrogenase, 25-Hydroxy-Vitamin-D-alpha-Hydroxylase-Defizienz, Artheriosklerose, Arzneimittelintoleranz, Automated High-Throughput Sequence Analysis, Auftragssequenzierungen, Ateriosclerosis, Arzneimittel und Genetik, APC-Resistenz, Antithrombin III Mangel, Antithrombin-Gen, Aromatase-Mangel, Aarskog Syndrom, Albright-Syndrom, Angiotensin konvertierendes Enzym, ACE, Apolipoporotein AI/CIII, Apolipoprotein-Cluster Chrosom 11, ApoA1/CIII, Apolipoprotein AIV, ApoA4, Apolipoprotein AV, ApoA5, Apolipoprotein B, ApoB 100, Apolipoprotein E, ApoE, ATP-Binding Cassette Transporter A 1, ABCA1-Gen, Arginin Vasopressin-Gen, Alkalische Phosphatase Leber/Niere/Knochen, ALPL, Autoimmunregulator-Gen, AIRE, Androgen-Resistenz, Androgen Rezeptor Gen, AR, Azoospermiefaktor Yq11, AZF, Aryl Hydrocarbon Hydroxylase, Aromatic compound inducible, Arylamine N-Acetyl transferase Type 2, Androgenrezeptor-Gen, CAG-Repeat, SMA, Bioglobe, Biotechnologie, Biotechnology, beta-ThalassÃ¤mie, cDNA, Cancer, chronic diseases, Carnitin Defizienz, Catechol-O-Methyltransferase, Catechol- und Ã–strogenkatabolismus, Cholesterolester Transferprotein, Collagen-1A1-Gen, Calcium-Sensing- Rezeptor-Gen, Collagen-1A1-Gen, COL1A1, CYP27B1, Cystische Fibrose, Zystische Fibrose, CBAVD, CFTR1, Cytochrom P450 1A1, Cyp1A1, Cytochrom P450 1A2, Cytochrom P450 1B1 , Cyp1B1, Cytochrom P450 2A6, Coumarin 7-Hydroxylase, Cyp2A6, Cytochrom P450 2C9, Cyp2C9, Cytochrom P450 2C19, Cyp2C19, Cytochrom P450 2D6, Cyp2D6, Cytochrom P450 2E1, Cyp2E1, Cytochrom P450 3A4, CC Chemokine Receptor, CCR5, Cytokine Synthesis Inhibitory Factor, Chronisch progressive externe Ophtalmoplegie, CPEO, Deutschland, DNA, Diagnostics, Diagnose, Diagnostik, Detoxification, Diabetes, DNA Sequencing, Discovery Disease Risks, Diabetes insipidus, NeurohypophysÃ¤rer Typ, Deafness and Goiter, Debrisoquine 4-Hydroxylase, Dihydropyrimidin Dehydrogenase, DPD, Dystrophin-Gen, Expression, Expressionsanalyse, Endokrinologie, Endocrinology, Effective Prevention, Ehlers-Danlos-Syndrom Typ VIIa, Exostosin 1, Exostosin 2, EXT2, endothelial, eNOS, Estrogen Receptor beta-Gen, ESRB, Ethanol inducible P450, Epoxide Hydroxylase, Faktor V-Leiden, Faktor V-Gen, Faktor 2-Gen, Faciogenitale Dysplasie 1, FamiliÃ¤rer Hyperaldosteronismus, FamiliÃ¤re HypercholesterinÃ¤mie, FamiliÃ¤re hypocalciurische Hyper- und HypocalcÃ¤mie, FamiliÃ¤res Mittelmeerfieber, FamiliÃ¤re SchilddrÃ¼senhormonresistenz, Fluoruracil-ToxizitÃ¤t, Fatty acid ethyl ester synthase III, Germany, Genom, Genotypisierungen, Genomanalyse, Genomics, Gene Mapping, Gendefekte, Genetisches Risikoprofil, Genomic Services, Gene, Genomic Profiles, Genetics, Genetic Risks, Guanin-Nucleotid-Bindungsprotein, Glucocorticoid supprimierbar, Guanin-Nucleotid-Bindungsprotein, GNAS, Glucocorticoid inducible P450, Glutathion-S-Transferase M1, GSTM1, Glutathion-S-Transferase T1, GSTT1, Glutathion-S-Transferase P1, GSTP1, Glucokinase, GCK, Hamburg, HÃ¶ppner, Hoeppner, High-Performance Services, HyperandrogenÃ¤mie, Hyperandrogenemy, Heart Attack, Herzanfall, Herzinfarkt, Healthcare, HÃ¤mochromatose, HFE-Gen, High Density Bone Mass, HBM, HPT-Jaw Tumor Syndrome, HRTP2, HyperlipoproteinÃ¤mie Typ 1, HypophosphatÃ¤mie, HereditÃ¤r, Typ 1 und 2, Hyp1 und Hyp2, Hypophosphatasie, Human Fibroblast Stromelysin, HÃ¤moglobin-ÃŸ-Locus, HPT-Jaw Tumor Syndrome, HRTP2, HereditÃ¤re non-polypÃ¶se Colon-Karzinome, HNPCC, Hamatomas intestinal polyposis, Hydroxylamin, HIV-SuszeptibilitÃ¤t, Hepatic Nuclear Factor 1alpha, HNF1alpha/TCF1, Immunologie, Immunology, Intolerance of Medication, I/D-Polymorphismus, Interleukin 1a, IL1a-Gen, Interleukin 1b, IL1b-Gen, Interleukin 6, Interferon-beta-2-Gen, IL6, Interleukin 10, IL10-Gen, Krankheitsrisiken, Krebs, KLOTHO, Kearns-Sayre-Syndrom, KSS, Kennedy's Disease, Lebenswissenschaften, Life Sciences, Life Science Technologies, Life Science Technology Services for Research and Development, Lipid-Transfer-Protein, LDL-Rezeptor-Gen, Lipoproteinlipase-Gen, Longevity, Li Fraumeni-Syndrom, Leber- und Fibroblasten-spezifisch, Leber- und Erythrozyten-spezifisch, Leber'sche hereditÃ¤re Opticus Neuropathie, LHON, Leigh-Syndrome, Lactat acidosis, Medical Genetics, Medizinische Genetik, Molekulare Diagnostik, Molecular Diagnostics, molekular, molecular, mRNA, MALDI-TOF Mass Spectrometry, Microarray Analyser, Molekularbiologie, Medical Biotechnology, Methylation Pattern Analysis, Multiple Pathogen Typing, Methylentetrahydrofolat-Reduktase, MTHFR-Gen, Matrix Metalloproteinase 3, McCune-Albright Syndrome, Multiple Exostosis Type 1, Multiple Osteochondromatose Typ 1, Multiple Exostosis Type 2, MÃ¤nnlicher Pseudohermaphroditismus, Multiple endokrine Neoplasie Typ 1, MEN 1-Gen, Multiple endokrine Neoplasie Typ 2, Multiples PhÃ¤ochromocytom, Mikrosatelliten-InstabilitÃ¤t, Microsomal Monooxidase, Mephenytoin 4-Hydroxylase, Microsomal, EPHX, Mercaptopurin-ToxizitÃ¤t, MODY Typ 2, MODY Typ 3, Mitochondrial induzierter Diabetes, mt-tRNA Leu(UUR), mt-tRNA-Leu(UUR), Muskeldystrophie Duchenne/Becker, Myoclonic Epilepsy, MELAS, MERRF, Marrow-Pancreas Syndrome, Neurology, Neurologie, Nitroxid Syntase Typ 3, Neurofibromatose Typ, Neurofibromin-Gen, NF1, Nifedipin Hydroxylase, N-Acetyl-Transferase Typ2, NAT2, Necrotizing encephalopathy, Neuropathie, Ataxie und Retinitis Pigmentosa, NARP, Oncology, Onkologie, Osteoporosis, Osteoporose, Ã–strogen-ÃŸ-Rezeptor, Osteogenesis Imperfecta Typ I und Typ III , Osteoporosis Pseudoglioma Syndrom, OPP, Osteochondrodysplasie, Prof. Dr. Wolfgang HÃ¶ppner, Pharmakogenetik, Pharmaceutical Biotechnology, Pharmacogenetics, Pregnancy Risks, Predictive Genomic Profiles, Personalized Healthcare, Preventive Biomedicine, Proteomics, Prothrombin, Protein C-Mangel, Protein C-Gen, Protein S-Mangel, Protein S-alpha-Gen, Plasminogenaktivator Inhibitor 1, Parafibromin-Gen, Paraoxonase, PON1, Pendred-Syndrome, Peroxisome Proliferator activated Receptor alpha, PPARA, Peroxisome Proliferator activated Receptor, PPARG, PolyglandulÃ¤re endokrine Insuffizienz Typ I, Pseudo-Vitamin-D-resistente Rachitis, Paragangliom, Parafibromin-Gen, Peutz-Jeghers Syndrom, Polymerase-Gamma, POLG1, Pearson Syndrome, real time PCR, RT-PCR, RNA, Recurrent Polyserositis, Rezeptor fÃ¼r thyreotropes Hormon, RET-Protoonkogen, Ribonuclease L, RNAsel, red ragged fibers, SNP, SNP-Genotyping, SNP-Frequency Analysis, SNP-Discovery, Sequence analysis, sequencing, sequencing service, Sequenzierung, Services for Industry and Universities, Services for Medical Doctors, Services for Academic Research Institutes, Services for Pharmaceutical Industry, Services for Biotechnology Companies, Screening, Sciance, Sciance Guards, Stroke, Schlaganfallrisiko, Schlaganfall, Schwangerschaftsrisiken, Serinproteinase-Inhibitor 1, Steroid-21-Hydroxylase-Mangel, Steroid-11-beta-Hydroxylase-Mangel, Steroid-17-alpha-Hydroxylase, Steroid-3-beta-Dehydrogenase-Mangel, Solute Carrier Family 22 member 5, SchilddrÃ¼senhormon-beta-Rezeptor, SuszeptibilitÃ¤t fÃ¼r KHK, Solute carrier Family 26 Member 4, SLC26A4, SpondyloepiphysÃ¤re Dysplasie tarda, SEDL, Steroid-5a-Reduktase2, SRDA2, Succinat Dehydrogenase Subunit D, SDHD-Gen, Dehydrogenase Subunit B, SDHB-Gen, Serin/Threonin Proteinkinase 11-Gen, Sulfotransferase 1A1, SULT1A1, Sulfotransferase 1C1, SULT1C1, Superoxid Dismutase Typ 2, SOD2, Superoxid Dismutase Typ 3, SOD3, Stroke like episodes, Sideroblastic anemia, Spinale und bulbÃ¤re Muskelatrophie SMAX1, Thrombosis, Thrombose, Technical Support, Thrombophilia, Thrombophilie, TestikulÃ¤re Feminisierung, TSH-Resistenz, TSHR, Tumorsuppressor-Gen p53, TP53, Thiopurine-S-Methyltransferase, TPMT, Transforming Growth Factor beta , TGFB1-Gen, Transforming Growth Factor beta Receptor, TGFBR1-Gen, Tumor-Necrosis-Factor-alpha, TNFalpha-Gen, Vitamin-D-resistente Rachitis, Vitamin-D-Resistenz, Vitamin-D-Rezeptor-Gen, VDR, Von Hippel-Lindau-Syndrom,, VHL-Gen, Wolfram-Syndrom, Wolframin-Gen, Warfarin/Tolbutamid-Hydroxylierung, X-chromosomal
Name: Description
Content: BioGlobe, Molecular Genetic Laboratory, leader in the field of molecular diagnostics

Server / Hosting

IP: 217.160.231.194
Latitude: 51.30
Longitude: 9.49
Country: Germany

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