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Research 541–570 of 1000+
- <i>Saccharomyces cerevisiae</i> BLYAS, a New Bioluminescent Bioreporter for Detection of Androgenic Compounds
- A preliminary study of finasteride in Tourette syndrome
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- 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
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- TMPRSS2: A Key Host Factor in SARS-CoV-2 Infection and Potential Therapeutic Target
- Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- LB943 Tofacitinib treatment of inflammatory skin conditions in patients with Down Syndrome
- Ectodermal Dysplasia: Variable Expressions
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Hair in the Wrong Place
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- Genetic prediction of male pattern baldness
- Wnt signaling in skin organogenesis
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- The PDGF/PDGFR pathway as a drug target
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Interferon in the treatment of cutaneous T-cell lymphoma
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Diagnosis and treatment of polonium poisoning
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Skin steroidogenesis in health and disease
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management