AAAAAA

   
Results: 1-8 |
Results: 8
MISSENSE MUTATIONS IN KERATIN-17 CAUSE EITHER PACHYONYCHIA-CONGENITA TYPE-2 OR A PHENOTYPE RESEMBLING STEATOCYSTOMA MULTIPLEX
Authors: 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
Citation: Fjd. Smith et al., MISSENSE MUTATIONS IN KERATIN-17 CAUSE EITHER PACHYONYCHIA-CONGENITA TYPE-2 OR A PHENOTYPE RESEMBLING STEATOCYSTOMA MULTIPLEX, Journal of investigative dermatology, 108(2), 1997, pp. 220-223
THE EFFECT OF A MUTATION IN K16 ON KERATIN FILAMENT DYNAMICS IN-VITRO
Authors: RUGG EL MCLEAN WHI PRESCOTT AR RATNAVEL R LEIGH IM MUNRO CS LANE EB
Citation: El. Rugg et al., THE EFFECT OF A MUTATION IN K16 ON KERATIN FILAMENT DYNAMICS IN-VITRO, Journal of investigative dermatology, 106(4), 1996, pp. 46-46
GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA- EVIDENCE FOR HETEROGENEITY
Authors: KELSELL DP STEVENS HP RATNAVEL R BRYANT SP BISHOP DT LEIGH IM SPURR NK
Citation: Dp. Kelsell et al., GENETIC-LINKAGE STUDIES IN NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA- EVIDENCE FOR HETEROGENEITY, Human molecular genetics, 4(6), 1995, pp. 1021-1025
PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATIN-16 AND KERATIN-17
Authors: MCLEAN WHI SMITH FJD CORDEN L RUGG EL LUNNY DP MORLEY SM SWENSSON O DOPPINGHEPENSTAL PJC GRIFFITHS WAD EADY RAJ RATNAVEL R HIGGINS C NAVSARIA H LEIGH IM MOSS C MCKENNA KE BINGHAM EA KUNKELER L MUNRO CS LANE EB
Citation: Whi. Mclean et al., PACHYONYCHIA-CONGENITA IS CAUSED BY MUTATIONS IN KERATIN-16 AND KERATIN-17, Journal of investigative dermatology, 105(3), 1995, pp. 454-454
BOWEL EVANS-SYNDROME IS LIKED TO 17Q24 BUT AN IDENTICAL CUTANEOUS PHENOTYPE CAN RESULT FROM K16 MUTATIONS
Authors: STEVENS HP KELSELL DP SHAMSHER M RATNAVEL R NAVSARIA HA SPURR N BISHOP DT BRYANT SP MARGER D MARGER FS GRIFFITHS WAD LEIGH IM
Citation: Hp. Stevens et al., BOWEL EVANS-SYNDROME IS LIKED TO 17Q24 BUT AN IDENTICAL CUTANEOUS PHENOTYPE CAN RESULT FROM K16 MUTATIONS, Journal of investigative dermatology, 105(3), 1995, pp. 456-456
IDENTIFICATION OF NOVEL MUTATIONS IN KERATIN-16 GENE IN 2-FAMILIES WITH FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK)
Authors: LEIGH M SHAMSHER M STEVENS HP RATNAVEL R PURKIS PE GRIFFITHS WAD MCLEAN WHI
Citation: M. Leigh et al., IDENTIFICATION OF NOVEL MUTATIONS IN KERATIN-16 GENE IN 2-FAMILIES WITH FOCAL NON-EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (NEPPK), Journal of investigative dermatology, 104(4), 1995, pp. 582-582
MUTATION OF KERATIN-9 GENE IN EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (EPPK)
Authors: SHAMSHER M NAVSARIA HA RATNAVEL R MCLEAN I LANE EB GRIFFITHS WAD LEIGH IM
Citation: M. Shamsher et al., MUTATION OF KERATIN-9 GENE IN EPIDERMOLYTIC PALMOPLANTAR KERATODERMA (EPPK), Journal of investigative dermatology, 103(3), 1994, pp. 427-427
RHEUMATOID-ARTHRITIS IN A PATIENT WITH PRIMARY HYPOGAMMAGLOBULINEMIA
Authors: HERMASZEWSKI R RATNAVEL R WEBSTER ADB DENMAN AM
Citation: R. Hermaszewski et al., RHEUMATOID-ARTHRITIS IN A PATIENT WITH PRIMARY HYPOGAMMAGLOBULINEMIA, British journal of rheumatology, 32(7), 1993, pp. 636-639
Risultati: 1-8 |