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Research 751–780 of 799
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Deciphering the microbiology of hidradenitis suppurativa: a step forward towards understanding an enigmatic inflammatory skin disease
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Ontogeny of Skin Stem Cells and Molecular Underpinnings
- An overview of current strategies and future prospects in drug repurposing in tuberculosis
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Testicular Steroidogenesis
- Expression and localization of Artemis serine 516 phosphorylation in human scalp skin
- Marie-unna hereditary hypotrichosis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Desmogleins: Hair perspective
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Central centrifugal cicatricial alopecia in Black men: A case series highlighting key clinical features in this cohort
- Frontal fibrosing alopecia: A review of disease pathogenesis
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
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- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Comparative immunohistochemical analysis suggests a conserved role of EPS8L1 in epidermal and hair follicle barriers of mammals
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome