Cockayne syndrome (CS), also called Neill-Dingwall syndrome, is a rare and fatal autosomal recessive neurodegenerative disorder characterized by growth...

Examples of PS include Werner syndrome (WS), Bloom syndrome (BS), Rothmund–Thomson syndrome (RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP)...

of syndromes; XP, trichothiodystrophy (TTD), or a combination of XP and Cockayne syndrome (XPCS). Both trichothiodystrophy and Cockayne syndrome display...

position 11.23. Having 1 or more copies of a mutated ERCC6 causes Cockayne syndrome, type II. DNA can be damaged by ultraviolet radiation, toxins, radioactive...

exhibit signs similar to Usher syndrome, including Alport syndrome, Alström syndrome, Bardet–Biedl syndrome, Cockayne syndrome, spondyloepiphyseal dysplasia...

cells. Unlike other "accelerated aging diseases" (such as Werner syndrome, Cockayne syndrome or xeroderma pigmentosum), progeria may not be directly caused...

Solid 2: Sons of Liberty. Accelerated aging disease Biogerontology Cockayne syndrome DNA repair Degenerative disease Genetic disorder Life extension Progeria...

Localized epidermolysis bullosa simplex Also known as "Weber–Cockayne syndrome": 460  and "Weber–Cockayne variant of generalized epidermolysis bullosa simplex"...

isolated syndrome CLOVES syndrome COACH syndrome Cobb syndrome Cockayne syndrome Coffin–Lowry syndrome Coffin–Siris syndrome Cogan syndrome Cohen syndrome Compartment...

хeroderma pigmentosum and CSA and CSB represent proteins linked to Cockayne syndrome. Additionally, the proteins ERCC1, RPA, RAD23A, RAD23B, and others...