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Research 601–630 of 1000+
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Advancements and Applications of Injectable Hydrogel Composites in Biomedical Research and Therapy
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Lean Women with Polycystic Ovary Syndrome
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Discreet monilethrix: De novo mutation on the example of polish families
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Connexin mutations in human disease
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- Trichothiodystrophy in a child with occult learning disorder
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Hypotrichosis in a child with olmsted syndrome
- The developmental basis of fingerprint pattern formation and variation
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- Frizzled Receptors in Development and Disease
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans