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Research 631–660 of 1000+
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Wounds and the Microbiota: The Healing Interplay Between Host and Microbial Communities
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Novel potential therapeutic targets of alopecia areata
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Impact of Reporter Type on Signal Detection of Cancer Therapy–Induced Alopecia: A Hypothesis-Generating Study Using the FDA Adverse Event Reporting System
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Exploring the Association Between Multidimensional Dietary Patterns and Non-Scarring Hair Loss Using Mendelian Randomization
- Causal Link of Distinct Mental Disorders with Androgenetic Alopecia and Alopecia Areata: A Bidirectional Two-Sample Mendelian Randomization Study
- Causal Relationship Between Blood Metabolomics and Female Pattern Hair Loss: A Bidirectional Mendelian Randomization Study
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Integration Analysis of Transcriptome Sequencing and Whole-Genome Resequencing Reveal Wool Quality-Associated Key Genes in Zhexi Angora Rabbits
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
- The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- EMT Factors and Metabolic Pathways in Cancer
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Alopecia areata: What’s new in the epidemiology, comorbidities, and pathogenesis?
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Is There a Histone Code for Cellular Quiescence?