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Research 241–270 of 1000+
- Trichotillomania Across Circuits: Neurobiology, Sensory Processing, and Genetic Insights
- Trichotillomania Across Circuits: Neurobiology, Sensory Processing, and Genetic Insights
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- IV Międzynarodowe Sympozjum Studenckich Kół Naukowych Środowisko – Roślina – Zwierzę – Produkt Streszczenia
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Alopecia Areata
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Ferreting out stem cells from their niches
- Pharmacologic interventions in aging hair
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Madarosis
- LSD1 is Required for Hair Cell Regeneration in Zebrafish
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Defective Expression of the Gap Junction Protein Pannexin-1 Channel Contributes to the Formation of PCOS-Realted Androgenetic Alopecia
- Follicular Neutrophilic Inflammation (Hidradenitis Suppurativa)
- Androgenetska alopecija u žena
- The pharmacology of methotrexate
- Endocrine Influences on Hair Growth
- Secondary cicatricial and other permanent alopecias
- Targeted Knockout of β-Catenin in Adult Melanocyte Stem Cells Using a Mouse Line, Dct::CreERT2, Results in Disrupted Stem Cell Renewal and Pigmentation Defects
- Inherited Disorders of the Hair
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Hair shaft disorders
- The role of vitamin D receptor signaling in hair follicle health and alopecia: Current understanding and therapeutic implications
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica