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Research 31–60 of 1000+
- Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Towards a molecular understanding of hair loss and its treatment
- A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation
- Acne
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- FEATURES OF DIAGNOSIS OF POSTCOVID ALOPECIA
- Androgenic alopecia. The main treatment options
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- An Update of Congenital Adrenal Hyperplasia
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Nonclassic 21-hydroxylase deficiency
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- 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.
- Congenital hair loss disorders: Rare, but not too rare
- Understanding Pattern Hair Loss—Hair Biology Impacted by Genes, Androgens, Prostaglandins and Epigenetic Factors
- Co‐regulatory mechanisms and potential markers of oxidative stress‐related genes in vitiligo and alopecia areata
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Gene expression profiling of human keratinocytes exposed to the hair-dying agent, m-aminophenol
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Female Androgenetic (?) Alopecia
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- In silico analysis of gene expression data from bald frontal and haired occipital scalp to identify candidate genes in male androgenetic alopecia