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Research 361–390 of 1000+
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- The molecular pathogenesis of Trichilemmal carcinoma
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Comparing Current Therapeutic Modalities of Androgenic Alopecia: A Literature Review of Clinical Trials
- Palatogenesis and cutaneous repair: A two‐headed coin
- A Clinical Study of Androgenetic Alopecia (V)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Interleukin 15 Gene Polymorphism in patients with Alopecia Areata
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Chronic overlapping pain conditions and nociplastic pain
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- Genome-Wide Association Studies of Hair Whorl in Pigs
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Investigations of 13 Genes in Non-Cicatricial Alopecia
- DNMT3B -579G>T POLYMORPHİSM AND THE RİSK OF COLORECTAL CANCER IN AZERBAİJAN POPULATİON
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses