Search
for
Sort by
Research 931–960 of 1000+
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- The Role of Micronutrients in Young Men Presenting with Hair Loss
- The Role of Propioni Bacterium acnes in Acne Vulgaris
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- The Role of Nutrition on Thyroid Function
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Joint Public Review: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- The Role of Vitamins and Minerals in Hair Loss: A Review
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- eLife assessment: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Lichen Planopilaris
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- Biochemical Evidence That Small Proline-rich Proteins and Trichohyalin Function in Epithelia by Modulation of the Biomechanical Properties of Their Cornified Cell Envelopes
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- Elucidating the roles of three β-glucuronosyltransferases (GLCATs) acting on arabinogalactan-proteins using a CRISPR-Cas9 multiplexing approach in Arabidopsis
- Androgenetic alopecia: combing the hair follicle signaling pathways for new therapeutic targets and more effective treatment options
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Biotinidase deficiency characterized by skin and hair findings
- An overview of the genetic aspects of hair loss and its connection with nutrition
- Hormone und Haarwachstum
- Hair Changes due to Drugs
- What is the Rationale for Androgen Therapy for Women?
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Epimorphic regeneration in mice is p53-independent