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Research 151–180 of 1000+
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- SEXUAL DIMORPHISM IN MAMMALS
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Genetic and molecular aspects of androgenetic alopecia
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- The Roles of EDA2R in Ageing and Disease
- It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Androgenetic Alopecia in Men: An Update On Genetics
- British Society for Dermatopathology
- Molecular genetics of androgen insensitivity
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Cosmeceutical Treatments for Androgenetic Alopecia
- Social selection favours offspring prone to the development of androgenetic alopecia.
- The genetics of androgenetic alopecia
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Disorders of Sex Development
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes