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Research 271–300 of 1000+
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Pili Annulati
- A phase 2a study investigating the effects of ritlecitinib on brainstem auditory evoked potentials and intraepidermal nerve fiber histology in adults with alopecia areata
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- The emerging roles of N6-methyladenosine (m6A) deregulation in polycystic ovary syndrome
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- Zebrafish Model of Hereditary Pigmentary Disorders
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- A different approach to PCOS: evaluation of spermiogram results in male patients with a family history of PCOS
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- A missense mutation in Lama3 causes androgen alopecia
- Role of the SOX family in cancer immune evasion: Emerging player and promising therapeutic opportunities
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Ichthyosis
- Hormonal Effects on Hair Follicles
- Androgen Action in the Ovary
- Hair follicle stem cell replication stress drives IFI16/STING-dependent inflammation in hidradenitis suppurativa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- The significance of the apelinergic system in doxorubicin-induced cardiotoxicity
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome