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Research 931–960 of 1000+
- Molecular studies of Hutchinson-Gilford progeria syndrome
- Central Precocious Puberty and Sjogren-Larsson Syndrome in a Child: A Rare Case Report
- In This Issue
- Identification of the cell lineage at the origin of basal cell carcinoma
- Association of the KAP 8.1 Gene Polymorphisms with Fibre Traits in Inner Mongolian Cashmere Goats
- Ichthyosis hystrix
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Collet Hairs Are Critical for Anchoring and Survival of <i>Arabidopsis thaliana</i> Seedlings During Early Development
- A phosphoinositide-mediated switch of GET pathway receptor dimerization in <i>Arabidopsis</i>
- Table 2_Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review.xlsx
- Observational Study of Paclitaxel-Carboplatin versus Pemetrexed-Carboplatin for Advanced Pulmonary Adenocarcinoma at Single-Centre in Indonesia
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Clinical Snippets
- The Endocrine Function of the Skin: An Analytical Narrative
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Netherton Syndrome Associated with Growth Hormone Deficiency
- <i>WNT10A</i> , dermatology and dentistry
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Atrichia with Papular Lesions: Dermoscopy to the Rescue
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Localizing the ROS Signal
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Clinical biochemistry of dihydrotestosterone
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Dysfunction of keratinocyte adhesion