Search
for
Sort by
Research 511–540 of 1000+
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Dermatoses of pregnancy
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Is polycystic ovary syndrome a sexual conflict? A review
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- NUDT15 polymorphism explains serious toxicity to azathioprine in Indian patients with chronic immune thrombocytopenia and autoimmune hemolytic anemia: a case series
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Androgen excess: a hallmark of polycystic ovary syndrome
- British Society for Dermatopathology
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- Alopecia Areata: Current Review
- 1338 Dermal Wnt/β-catenin activation tunably controls hair follicle initiation
- 1336 The de novo DNA methyltransferase DNMT3A is required for epidermal homeostasis
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Hairline Lowering
- Inherited Epidermolysis Bullosa: A Clinical Case
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- <i>Hoxc13</i> mutant mice lack external hair
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Drug-Induced Skin, Nail and Hair Disorders
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase