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Research 211–240 of 1000+
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Efficacy and Safety of Laser Therapy and Phototherapy in Cicatricial and NonCicatricial Alopecia: A Systematic Review Study
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- 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
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- SUMMARIES OF PAPERS
- Oral Manifestations of Hematologic and Nutritional Diseases
- Endocrine disorders and hormonal therapy for adolescent acne
- The Spectrum of Skin Disease Among Indian Children
- Acne and acneiform eruptions
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- A Comprehensive Review of Acne Vulgaris
- Uses, abundance perception, and potential geographical distribution of Smilax aristolochiifolia Mill (SMILACACEAE) on the Totonacapan Region of Puebla, Mexico
- Analogs of human genetic skin disease in domesticated animals
- Novel lysophosphoplipid receptors: their structure and function
- E-Poster
- Autotaxin–lysophosphatidic acid– LPA <sub>3</sub> signaling at the embryo‐epithelial boundary controls decidualization pathways
- Poster Presentations
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Genetic Variants and Protective Immunity against SARS-CoV-2
- 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