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Research 451–480 of 1000+
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Premature aging syndromes: From patients to mechanism
- 14-3-3σ Is Required for Club Hair Retention
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- An unusual presentation of X-linked adrenoleukodystrophy
- FOXN1 deficient nude severe combined immunodeficiency
- Establishment of Tsc2-deficient rat embryonic stem cells
- Converging physiological roles of the anthrax toxin receptors
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- White piedra and pediculosis capitis in the same patient
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- The parathyroid hormone-related protein as a regulator of normal tissue functions
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- New clinico‐genetic classification of trichothiodystrophy
- A review of genotrichoses and hair pathology associated with inherited skin diseases