Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' Corden, LD' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 13 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Corden, LD; McLean, WHI
      Keratins and keratin disorders

      CELL ADHESION AND MIGRATION IN SKIN DISEASE
    2. Porter, RM; Corden, LD; Lunny, DP; Smith, FJD; Lane, EB; McLean, WHI
      Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans

      BRITISH JOURNAL OF DERMATOLOGY
    3. Corden, LD; Swensson, O; Swensson, B; Smith, FJD; Rochels, R; Uitto, J; McLean, WHI
      Molecular genetics of Meesmann's corneal dystrophy: Ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene

      EXPERIMENTAL EYE RESEARCH
    4. Corden, LD; Swensson, O; Swensson, B; Rochels, R; Wannke, B; Thiel, HJ; McLean, WHI
      A novel keratin 12 mutation in a German kindred wi th Meesmann's corneal dystrophy

      BRITISH JOURNAL OF OPHTHALMOLOGY
    5. Sybert, VP; Francis, JS; Corden, LD; Smith, LT; Weaver, M; Stephens, K; McLean, WHI
      Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferredby mutations in the 2B domain of keratin K1

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. CORDEN LD; MELLERIO JE; GRATIAN MJ; EADY RAJ; HARPER JI; LACOUR M; MAGEE G; LANE EB; MCGRATH JA; MCLEAN WHI
      HOMOZYGOUS NONSENSE MUTATION IN HELIX-2 OF K14 CAUSES SEVERE RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX

      Human mutation
    7. IRVINE AD; CORDEN LD; SWENSSON O; SWENSSON B; MOORE JE; FRAZER DG; SMITH FJD; KNOWLTON RG; CHRISTOPHERS E; ROCHELS R; UITTO J; MCLEAN WHI
      MUTATIONS IN CORNEA-SPECIFIC KERATIN K3 OR K12 GENES CAUSE MEESMANNS CORNEAL-DYSTROPHY

      Nature genetics
    8. CORDEN LD; MELLERIO JE; GRATIAN MJ; EADY RAJ; HARPER JI; LACOUR M; MAGEE G; LANE EB; MCLEAN WHI; MCGRATH JA
      HOMOZYGOUS NONSENSE MUTATION IN THE HELIX-2 DOMAIN OF K14 CAUSES RECESSIVE EBS

      Journal of investigative dermatology
    9. SMITH FJD; CORDEN LD; RUGG EL; RATNAVEL R; LEIGH IM; MOSS C; TIDMAN MJ; HOHL D; HUBER M; KUNKELER L; MUNRO CS; LANE EB; MCLEAN WHI
      MISSENSE MUTATIONS IN KERATIN-17 CAUSE EITHER PACHYONYCHIA-CONGENITA TYPE-2 OR A PHENOTYPE RESEMBLING STEATOCYSTOMA MULTIPLEX

      Journal of investigative dermatology
    10. MCLEAN WHI; CORDEN LD; IRVINE AD; MOORE JE; FRAZER DG; SWENSSON O; SWENSSON B; SMITH FJD; KNOWLTON RG; CHRISTOPHERS E; ROCHELS R; UITTO J
      MEESMANNS-CORNEAL-DYSTROPHY IS CAUSED BY MUTATIONS IN CORNEA-SPECIFICKERATINS

      American journal of human genetics
    11. MCLEAN WHI; RUGG EL; SMITH FJD; MORLEY SM; SHEMANKO CC; CORDEN LD; MUNRO CS; LEIGH IM; EADY RAJ; LANE EB
      EB SIMPLEX AND THE GROWING FAMILY OF KERATIN DISEASES

      Journal of investigative dermatology
    12. JONKMAN MF; HEERES K; PAS HH; VANLUYN MJ; ELEMA JD; CORDEN LD; SMITH FJD; MCLEAN WHI; RAMAEKERS FCS; BURTON M; SCHEFFER H
      EFFECTS OF KERATIN-14 ABLATION ON THE CLINICAL AND CELLULAR PHENOTYPEIN A KINDRED WITH RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX

      Journal of investigative dermatology
    13. SMITH FJD; CORDEN LD; RUGG EL; MORLEY SM; LANE EB; HUBER M; HOHL D; MUNRO CS; MCLEAN WHI
      MUTATIONS IN KERATIN-17 CAUSE STEATOCYSTOMA MULTIPLEX

      Journal of investigative dermatology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/01/21 alle ore 13:18:50