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Research 301–330 of 1000+
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Spontaneous cutaneous adverse drug reaction reports—An analysis of a 10‐year dataset in Singapore
- MiR‐200c‐3p as a novel genetic marker and therapeutic tool for alopecia areata
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- The hair shaft: normality, abnormality, and genetics
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Hair Loss in Paediatric and Adolescent Age Group: A Clinico-Pathological Analysis in a Tertiary Health Care Centre
- Lipedematous Scalp Occurring in Two Female Siblings: Further Evidence for a Genetic Role
- Functional divergence of plant expansins as revealed by genetic complementation of root-hair tip growth in <i>Arabidopsis thaliana</i>
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- 072 Covid-19 and male androgenetic alopecia: Systematic investigation of a potential epidemiological and genetic association
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- The Prospect and Application Research Progress of Precision Gene Editing Technology Based on CRISPR/Cas9 in Livestock Genetics and Breeding
- The Effect of Hairless Mutant Gene on The Thymus and Skin Under The C_(57)BL/6 Genetic Background
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Platelet-Rich Plasma for Treating Androgenic Alopecia: A Systematic Review
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Discovery of genes and proteins possibly regulating mean wool fibre diameter using cDNA microarray and proteomic approaches