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Research 901–930 of 1000+
- Vitiligo – Study In view of familial occurence
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
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- Exploiting molecular genetic diagnoses of polycystic ovary syndrome to achieve better patient outcome
- Inherited Disorders of the Hair
- Research on Keratins Reveals Unexpected Link Between Hair Disorders and Dental Decay
- Modulation of Androgen Receptor Transcriptional Activity
- Molecular genetics of androgen insensitivity
- Discussion: Themes in the Molecular Structure of Hair
- Molecular Genetics of Inherited Disorders of Epidermal Keratins
- To be hairless or wise?
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia
- Multiple facial atrophic scars in childhood
- Influence of NUDT15 Genotyping on Dose Intensity of Thiopurine Administration and Long-Term Clinical Outcomes (Hospitalization and Surgery)
- 738 Cryo-EM and molecular dynamics of TRPV3 channel in activated state reveal structural features implicated in severe itch and hyperkeratosis
- Management of a Refractory EIF3E-RSPO2 Fusion Positive Pilomatrical Cancer Patient with Encyclopedic Tumor Analysis Guided Treatment
- Two females with hair loss
- Letter from Brisbane [Letters to editor]
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- The character “hairless” in the mouse
- Hair for brain trade-off, a metabolic bypass for encephalization
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- QuantAnts machines discover biomarkers for RAS signaling activation and design sgRNAs for CRISPR to target complex CD9, CD34, and CD74.
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- Types I and II Keratin Intermediate Filaments
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.