UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
B B B0 B1 B4 B7 B8 BA BB BC BD BE BF BG BH BI BK BL BM BN BO BP BR BS BT BU BV BW BX BY BZ
BE BE+ BEA BEB BEC BED BEE BEF BEG BEH BEI BEK BEL BEM BEN BEP BER BES BET BEU BEV BEX
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1. Becaplermin
[Expressed as 2 alternative isoforms in platelets by human PDGFB Gene (PDGF/VEGF Family), 241-aa 27-kDa (precursor) Platelet-Derived Growth Factor-Beta Chain is a potent mitogenic factor for mesenchymal cells characterized by a motif of eight cysteines and released by platelets upon wounding to stimulate adjacent cell growth. PDGFB can exist as either antiparallel disulfide-linked homodimers or heterodimers with Platelet-Derived Growth Factor Alpha. A-A, B-B, and A-B, dimers can bind to PDGF receptor and elicit a variety of cellular responses. A and B homodimers are implicated in transformation processes. PDGFB mutations are associated with meningioma. Reciprocal t(17;22)(q22;q13) translocations with COL1A1 result in unregulated growth factor expression and are associated with DFSP. (NCI) ( NCI )] (UMLS (NCI) C0072480) =Amino Acid, Peptide, or Protein; Biologically Active Substance ;
8. Beclomethasone Dipropionate Monohydrate
(UMLS (NCI) C0795584) =Steroid; Pharmacologic Substance ;
2. Beck Depression Inventory
[A twenty-one question survey completed by a patient, with each answer scored on a scale of 0 to 3, designed to measure presence of depression. ( NCI )] (UMLS (NCI) C0451022) =Diagnostic Procedure
9. Beclomethasone/Methylprednisolone
(UMLS (NCI) C1327890) =Therapeutic or Preventive Procedure ;
3. Becker's muscular dystrophy
[ ] (UMLS (CSP) C0917713) =Disease or Syndrome
10. Beclomethasone/Prednisone
(UMLS (NCI) C1327889) =Therapeutic or Preventive Procedure ;
4. Becker's Nevus
(UMLS (NCI) C0263579) =Neoplastic Process
11. Beclovent
(UMLS (NCI) C0699071) =Steroid; Pharmacologic Substance
5. Beckwith-Wiedemann Syndrome
[A syndrome of multiple defects characterized primarily by umbilical hernia (HERNIA, UMBILICAL); MACROGLOSSIA; and GIGANTISM; and secondarily by visceromegaly; HYPOGLYCEMIA; and ear abnormalities. ( MSH )] (UMLS (NCI) C0004903) =Congenital Abnormality; Disease or Syndrome ;
12. Beconase
(UMLS (NCI) C0591154) =Steroid; Pharmacologic Substance
6. Beckwith-Wiedemann Syndrome Chromosome Region 1, Candidate A
[Expressed predominantly in fetal and adult liver and kidney by human SLC22A1L Gene (Polyspecific Transporter/MDR Family), 424-aa Tumor Suppressing Subtransferable Candidate 5 Protein (Organic Cation Transporter-Like 2 Protein) is a polyspecific organic-cation transporter, containing 10 transmembrane segments, involved in excretion of endogenous and exogenous compounds. SLC22A1L translation may begin at the second methionine, which would result in a 408-amino acid protein. (NCI) ( NCI )] (UMLS (NCI) C0673602) =Amino Acid, Peptide, or Protein; Biologically Active Substance
13. Becquerel
[A SI derived unit of activity of a radionuclide, equal to one nuclear disintegration or other nuclear transition from a particular energy state occurring in an amount of a radionuclide during one second-long time interval. ( NCI )] (UMLS (NCI) C0560038) =Quantitative Concept =UnitOfMeasureAtomInsens;
UnitOfMeasureAtomSens
7. Beckwith-Wiedemann Syndrome Protein
[A negative regulator of cell proliferation, KIP2 is a tight-binding inhibitor of the G1 Cyclin E-CDK2, Cyclin D2-CDK4, and Cyclin A-CDK2 complexes, and also inhibits mitotic Cyclin B-CDC2. The N-terminal CDK inhibitory domain is similar to p21(CIP1). (from SWISS-PROT P49918, OMIM 600856, and NCI) ( NCI )] (UMLS (NCI) C0906558) CDKN1C;
CDKN1C Protein;
Cyclin-Dependent Kinase Inhibitor 1C;
Cyclin-Dependent Kinase Inhibitor p57;
KIP2 Protein;
p57-KIP2 Protein =Amino Acid, Peptide, or Protein; Biologically Active Substance ;

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