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Research 511–540 of 1000+
- Das weiße Hautfettgewebe initiiert die IL-33-abhängige Expression von Interleukin 4/13 in myeloischen Zellen während einer Entzündung
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Integrating herbal components into pharmaceutical formulations for hair woes
- Cosmetic Considerations in Dark-Skinned Patients
- Androgen excess: a hallmark of polycystic ovary syndrome
- Case report: Systemic granulomatous disease with vasculitis in a bull due to hairy vetch (Vicia villosa) toxicosis
- Signaling pathways in hair aging
- Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome
- FRI220 Primary Bilateral Macronodular Adrenal Hyperplasia: A Rare Cause Of Cushing Syndrome
- Inhibitory Effects of Pueraria mirifica Aqueous Extracts on 5α-reductase and Prostate Histomorphometry in Testosterone-induced Benign Prostatic Hyperplasia Sprague Dawley Rats
- En Coup de Sabre in a Pediatric Patient Treated With Calcipotriene
- Potential Pharmacological Activities of Pumpkin Seeds as a Functional Food: A Comprehensive Review
- Novel type 1 5a-reductase Inhibitors with Antiproliferative Potential on LNCaP cells
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- Hair loss after covid 19 - case series
- Evaluation of the palatal wound healing effect of wound dressing carrying GSK-3 antagonist tideglusib on rats
- 5 Alpha - Reductase and Metabolic Syndrome in PCOS Patients
- Dermal EZH2 simultaneously orchestrates dermal differentiation and epidermal proliferation during murine skin development
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Cicatricial Alopecia with Particular Trichoscopic and Histopathological Features
- WNT10B (wingless-type MMTV integration site family)
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Scalp Psoriasis
- Psychodermatology U.K.
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Benign Cutaneous Eruptions After Transplantation
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue