23 results on '"Hohl D"'
Search Results
2. Eccrine naevus: Case report with dermoscopic findings
3. Pitiriasis rubra pilaris
4. 483 PTCH1 inactivation is sufficient to cause basaloid follicular hamartoma in pediatric Nevoid basal cell carcinoma syndrome
5. Ther-PO-18 - Exacerbation of mycosis fungoides masquerading as psoriasis under cytokine-pathway blockers
6. 7-3 - Physiopathologie de la kératinisation
7. 7-4 - Ichtyoses
8. 168 ARP-T1-associated Bazex-Dupré-Christol Syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies
9. 1329 CENPV is a novel CYLD-interacting molecule regulating ciliary acetylated tubulin
10. 205 ARP-T1 is a protein associated with a novel ciliopathy in inherited basal cell cancer of Bazex-Dupré-Christol Syndrome
11. 485 Mutations in ACTRT1 and its transcribed non-coding elements lead to aberrant activation of the Hedgehog signaling pathway in inherited and sporadic basal cell carcinomas
12. Identification de la première mutation non-sens de la cornéodesmosine avec expression d’une protéine tronquée et causant un peeling skin syndrome, type B
13. Syndrome de Birt-Hogg-Dubé et sclérose tubéreuse de Bourneville : un défi histopathologique
14. Hidradénite eccrine à Pseudomonas de l’enfant révélatrice d’une leucémie aiguë lymphoblastique
15. Ichthyosiform dermatosis with superficial blister formation and peeling: Evidence for a desmosomal anomaly and altered epidermal vitamin A metabolism
16. Quantum effects in solid hydrogen at ultra-high pressure
17. First principles MD simulation of liquid and amorphous selenium
18. The structure of selenium clusters — Se 3 TO Se 8
19. The human loricrin gene.
20. Characterization of human loricrin. Structure and function of a new class of epidermal cell envelope proteins.
21. Identification of mutational hot spots in the suprabasal keratin genes from patients with epidermolytic hyperkeratosis
22. Repetin: A novel repetitive protein with putative EF-hands localised to the epidermal differentiation complex on 1q21
23. 102 Cornified cell envelope (CE) formation in Vohwinkel's syndrome (VS) is abnormal
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