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Encyclopedia results for ABCC2

ABCC2





Encyclopedia results for ABCC2

  1. Multidrug resistance-associated protein 2

    9284939 pmc doi 10.1159 000134599 ref ref name entrez cite web title Entrez Gene ABCC2 ATP binding ... N, Lindenmaier H, Haefeli WE title Inhibition of MRP1 ABCC1, MRP2 ABCC2, and MRP3 ABCC3 by nucleoside ... informahealthcare.com doi abs 10.1080 00498250500354493 20 issn refend External links MeshName ABCC2 ... inspection no update protein box yes update summary yes update citations no DEFAULTSORT Abcc2 Category ...   more details



  1. Transmembrane domain of ABC transporters

    ABCC13 ABCC2 ABCC3 ABCC4 ABCC5 ABCC6 ABCC8 ABCC9 Cystic fibrosis transmembrane conductance regulator ...   more details



  1. ATP-binding domain of ABC transporters

    ABCB7 ABCB8 ABCB9 ABCC1 ABCC10 ABCC11 ABCC12 ABCC2 ABCC3 ABCC4 ABCC5 ABCC6 ABCC8 ABCC9 ABCD1 ABCD2 ...   more details



  1. Organic anion transporter 1

    OAT1, SLC22A8 OAT3 , OATP4C1 , MDR1 , ABCC2 MRP2 , MRP4 and URAT1 are expressed in the Proximal ...   more details



  1. NFE2L2

    month March pmid 17259171 doi 10.1074 jbc.M610790200 url issn ref ABCC2 Multidrug resistance associated ...   more details



  1. Berberine

    1014 ref When applied in vitro and in combination with methoxyhydnocarpin, an inhibitor of ABCC2 multidrug ...   more details



  1. List of OMIM disorder codes

    context date January 2011 Below is a list of OMIM disorder codes 17,20 lyase deficiency, isolated OMIM2 202110 CYP17A1 17 alpha hydroxylase 17,20 lyase deficiency OMIM2 202110 CYP17A1 17 beta hydroxysteroid dehydrogenase X deficiency OMIM2 300438 HSD17B10 2 methylbutyrylglycinuria OMIM2 610006 ACADSB 3 hydroxyacyl CoA dehydrogenase deficiency OMIM2 231530 HADHSC 3 hydroxyisobutryl CoA hydrolase deficiency OMIM2 250620 HIBCH 3 M syndrome OMIM2 273750 CUL7 3 Methylcrotonyl CoA carboxylase 1 deficiency OMIM2 210200 MCCC1 3 Methylcrotonyl CoA carboxylase 2 deficiency OMIM2 210210 MCCC2 3 methylglutaconic aciduria, type I OMIM2 250950 AUH gene AUH 3 methylglutaconic aciduria, type III OMIM2 258501 OPA3 3 methylglutaconic aciduria, type V OMIM2 610198 DNAJC19 46XX true true hermaphroditism OMIM2 400045 SRY 46XY complete gonadal dysgenesis OMIM2 233420 DHH hedgehog DHH 46XY complete gonadal dysgenesis OMIM2 400044 SRY 46XY gonadal dysgenesis, complete or partial, with or without adrenal failure OMIM2 612965 NR5A1 46XY gonadal dysgenesis, complete, CBS2 related OMIM2 613080 CBX2 46XY partial gonadal dysgenesis, with minifascicular neuropathy OMIM2 607080 DHH hedgehog DHH 5 fluorouracil toxicity OMIM2 274270 DPYD 6 mercaptopurine sensitivity OMIM2 610460 TPMT Aarskog Scott syndrome OMIM2 305400 FGD1 ABCD syndrome OMIM2 600501 EDNRB Abetalipoproteinemia OMIM2 200100 MTP gene MTP ACAD9 deficiency OMIM2 611126 ACAD9 Acampomelic campomelic dysplasia OMIM2 114290 SOX9 Achalasia Addisonianism Alacrimia syndrome OMIM2 231550 AAAS gene AAAS Acheiropody OMIM2 200500 LMBR1 Achondrogenesis Ib OMIM2 600972 SLC26A2 Achondrogenesis type 1A OMIM2 200600 TRIP11 Achondrogenesis hypochondrogenesis type 2 OMIM2 200610 COL2A1 Achondroplasia OMIM2 100800 FGFR3 Achromatopsia 2 OMIM2 216900 CNGA3 Achromatopsia 3 OMIM2 262300 CNGB3 Acrocallosal syndrome OMIM2 200990 GLI3 Acrocapitofemoral dysplasia OMIM2 607778 IHH Acrodermatitis enteropathica OMIM2 201100 SLC39A4 Acrokeratosis verruciformis OMIM2 ...   more details




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