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Research 751–780 of 1000+
- Histopathologic Criteria for Follicular Differentiation
- Aberrant Wnt signalling induces comedo-like changes in the upper hair follicle
- Preparation and Characterization of Soluble Wool Keratin for Human Hair Care
- Nevus comedonicus syndrome: a case associated with multiple basal cell carcinomas and a rudimentary toe
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Efficacy of two traditionally used potentized homeopathic medicines, Calcarea carbonica and Lycopodium clavatum, used for treating PCOS patients: I. Effects on certain important external guiding symptoms
- Absence of chemotherapy-induced alopecia with paclitaxel in a case of hypothyroidism: case report
- EFFECTS OF HUMAN HAIR KERATIN ALKYLATION ON GROWTH FACTOR DELIVERY AND CELLULAR RESPONSE: IMPLICATIONS IN BONE REGENERATION
- The Utility of De-epithelialization in Subcutaneous Skin Flap Transposition.
- Irregular Menstruation, Acne, Hirsutism, and the Possibility with PCOS
- P‐51 Drug‐induced erythema multiforme or drug‐induced pemphigus foliaceus: a case report
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- The TIP GROWTH DEFECTIVE1 <i>S</i>-Acyl Transferase Regulates Plant Cell Growth in <i>Arabidopsis</i>
- Human hair keratins
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Onycholemmal Carcinoma
- An unusual variant of granulomatous adnexotropic cutaneous T-cell lymphoma
- Relationship between Amino Acid Intake and Accretion in a Marsupial, <i>Macropus Eugenii</i>
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Polycystic Ovarian Syndrome: Is It Time to Rename PCOS to HA-PODS?
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Mechanisms of Submucosal Gland Morphogenesis in the Airway
- Diagnostic delay, comorbid hidradenitis suppurativa and the prognostic value of bacterial culture in folliculitis decalvans: A cohort study
- Birt–Hogg–Dubé syndrome
- Differential expression of mTOR signaling pathway proteins in lichen planopilaris and frontal fibrosing alopecia
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Polycystic Ovary Syndrome (PCOS): From Diagnosis to Treatment
- A Case of Steatocystoma Multiplex in a Psoriatic Patient during Treatment with Anti-IL-12/23