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CDSN encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. Zusätzlich bieten wir Ihnen Corneodesmosin Kits (33) und Corneodesmosin Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 35 products:
Human Monoclonal Corneodesmosin Primary Antibody für ELISA, WB - ABIN560318
Fluhr, Lachmann, Baudouin, Msika, Darlenski, De Belilovsky, Bossert, Colomb, Burdin, Haftek: Development and organization of human stratum corneum after birth: electron microscopy isotropy score and immunocytochemical corneocyte labelling as epidermal maturation's markers in infancy. in The British journal of dermatology 2014
We found that a burden of low-frequency coding variants in N4BP2 (zeige N4BP2 Antikörper), CDSN, PRTG (zeige PRTG Antikörper), and AHRR (zeige CYP1A1 Antikörper) were associated with increased risk of Nonsyndromic cleft lip with or without cleft palate (NSCL (zeige NHLH1 Antikörper)/P) . Low-frequency variants in other genes were associated with decreased risk of NSCL (zeige NHLH1 Antikörper)/P. These results demonstrate that low-frequency variants contribute to the genetic etiology of NSCL (zeige NHLH1 Antikörper)/P
Investigated potential direct protein-protein interactions between six late cornified envelope (LCE (zeige ELOVL6 Antikörper)) proteins and two corneodesmosin sequence variants. Partial colocalization of LCE2 (zeige ELOVL6 Antikörper) and CDSN was observed in normal and psoriasis skin.
we report a patient with PSD (zeige PSD Antikörper) caused by a novel homozygous large deletion in the 6p21.3 region encompassing the CDSN gene, which abrogates CDSN expression
Case Report: homozygous deletion of CDSN was considered to be responsible for generalized peeling skin disease.
PSORS1C1 (zeige PSORS1C1 Antikörper)/CDSN gene may play a pathogenic role in ankylosing spondylitis
A nonsense mutation (C717G) in cDNA sequence of the CDSN gene was identified in all three patients of the family.
CDSN -619C/T polymorphism may not be associated with susceptibility to psoriasis.
CDSN plays a vital role in the structural and functional integrity of the epidermis and the hair follicle integrity by preventing the rupture of corneodesmosome.
identified mRNA transcripts from three genes CDSN, LOR (zeige LOR Antikörper) and KRT9 (zeige KRT9 Antikörper), showing strong over-expression in skin samples relative to samples from forensic body fluids, making them suitable markers for skin identification
Study of consangunity in a large family points to a homozygous nonesense mutation of the gene coding for corneodesmosin.
These results underscore the essential roles of CDSN in hair physiology and suggest functional relevance of CDSN gene polymorphisms to psoriasis susceptibility.
This gene encodes a protein found in corneodesmosomes, which localize to human epidermis and other cornified squamous epithelia. During maturation of the cornified layers, the protein undergoes a series of cleavages, which are thought to be required for desquamation. The gene is located in the major histocompatibility complex (MHC) class I region on chromosome 6.
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