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Research 121–150 of 1000+
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Disruption of microtubules with low intensity ultrasound rescues hair follicle damage by paclitaxel in mouse models
- Fibroblast bioelectric signaling drives hair growth
- Diseases of Hair
- Hair & Cutaneous Development
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Inherited Disorders of the Hair
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Thyroid hormones and androgens differentially regulate gene expression in testes and ovaries of sexually mature Silurana tropicalis
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- WNT10B (wingless-type MMTV integration site family)
- Menopause - Andropause - Anti-Aging 2008, 11.-13. Dezember 2008, Wien - Abstracts
- Congenital Adrenal Hyperplasia
- Trichoscopy in Hair Shaft Disorders
- Artificial skin for wound healing
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Adrenal causes of endocrine hypertension in childhood or adolescence
- <i>Hoxc13</i> mutant mice lack external hair