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Research 301–330 of 1000+
- Estrogens and the skin
- Follicular Transplantation
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Medical dermatologic conditions in transgender women
- The E6/E7 oncogenes of human papilloma virus and estradiol regulate hedgehog signaling activity in a murine model of cervical cancer
- CONTRACEPTION AND THE SKIN
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Managing patterned hair loss – a hair raising task!
- Topikal Retinoidler
- Scalp Dermatology for the Hair Restoration Surgeon: Scalp Lesions
- The Efficacy and Safety of Dr. SKS Hair Booster Serum (a Cocktail of Micronutrients and Multivitamins) in Adult Males and Females With Androgenetic Alopecia: An Open-Label, Non-randomized, Prospective Study
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Molecular Genetics of Alopecias
- Trichoscopy in genetic hair shaft abnormalities
- Functional ectodermal organ regeneration as the next generation of organ replacement therapy
- Biotin
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Canine alopecia X
- Molecular Genetics of Human Hair Diseases
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy