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cgp 12177 and Dermatitis, Atopic

cgp 12177 has been researched along with Dermatitis, Atopic in 1 studies

CGP 12177 : A benzimidazole that is benzimidazol-2-one substituted at position 4 by a 3-(tert-butylamino)-2-hydroxypropoxy group.

Dermatitis, Atopic: A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.

Research Excerpts

ExcerptRelevanceReference
"DNA sequence analysis of nine atopic eczema patients confirmed a substitution in codon (1618) GCC (Ala(119)) to GAC (Asp(119))."1.34Structural and functional alterations in the beta2-adrenoceptor are caused by a point mutation in patients with atopic eczema. ( Gibbons, NC; Pittelkow, MR; Schallreuter, KU; Swanson, NN; Wei, Y; Wood, JM, 2007)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Schallreuter, KU1
Wei, Y1
Pittelkow, MR1
Swanson, NN1
Gibbons, NC1
Wood, JM1

Other Studies

1 other study available for cgp 12177 and Dermatitis, Atopic

ArticleYear
Structural and functional alterations in the beta2-adrenoceptor are caused by a point mutation in patients with atopic eczema.
    Experimental dermatology, 2007, Volume: 16, Issue:10

    Topics: Adolescent; Adrenergic beta-Antagonists; Adult; Amino Acid Sequence; Amino Acid Substitution; Base S

2007