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Research 331–360 of 866
- Le gène<i>hairless</i>de la souris
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Learning from nudity: lessons from the nude phenotype
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Regulatory T Cells: the Many Faces of Foxp3
- Biology and Genetics of Hair
- How to diagnose a lipodystrophy syndrome
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- 5-Alpha reductase deficiency
- Morphological Approach to Hair Disorders
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Hairless is a nuclear receptor corepressor essential for skin function
- Diagnostic approach to low‐renin hypertension
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Dermatopathology and molecular genetics
- Inherited Disorders of the Hair
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- The Role of Histone Demethylases in Disease
- Adrenal causes of endocrine hypertension in childhood or adolescence
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Acne-Associated Syndromes
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Genetic Defects of Female Sexual Differentiation