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Research 31–60 of 815
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Biotinidase deficiency characterized by skin and hair findings
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Dermal Microvascular Responses of Human Induced Pluripotent Stem Cell–Derived Skin Organoids to Inflammation and Injury
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Vestibular Hair Cell Regeneration and Restoration of Balance Function Induced by Math1 Gene Transfer
- Development of a Novel Mouse Model for Hair Regeneration Using Glue-like Adhesive Materials
- Human pluripotent stem cell-derived skin organoids enabled pathophysiological model of Mycobacterium tuberculosis infection
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Reporting on Adverse Clinical Events
- Contents
- Delayed Puberty
- Comment on Malloy (2008) “James Watson tells the inconvenient truth: Faces the consequences”
- Hair morphogenesis<i>in vitro</i>: formation of hair structures suitable for implantation
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Experiences of discrimination during pregnancy predict altered neonatal hair cortisol at birth
- Ocular manifestations in a case of Kallmann syndrome – An interesting case report on isolated gonadotropin-releasing hormone deficiency
- Visualising Androgen Receptor Activity in Male and Female Mice
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- A guide to diagnosis and management of hypertrichosis
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Reproduction of the human relevant potency threshold (HRPT) for estrogen receptor alpha agonism in an inference performance screen for ICCVAM’s regulatory scientific confidence framework
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Congenital Adrenal Hyperplasia
- Design of In Vitro Hair Follicles for Different Applications in the Treatment of Alopecia—A Review
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy