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Research 181–210 of 1000+
- Screening of Protein Related to Wool Development and Fineness in Gansu Alpine Fine-Wool Sheep
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- 196 The endocannabinoid tone regulates human sebocyte biology
- SUMMARIES OF PAPERS
- LITERATURE REVIEW
- Male fertility and skin diseases
- The Spectrum of Skin Disease Among Indian Children
- National scientific medical meeting 1996 abstracts
- Modelling androgen synthesis and action during human sexual differentiation
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Novel lysophosphoplipid receptors: their structure and function
- Analogs of human genetic skin disease in domesticated animals
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Palatogenesis and cutaneous repair: A two‐headed coin
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study