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Research 61–90 of 1000+
- Assessment of chemokines MIP-1α and MIP-1 βin Iraqi women with polycystic ovarian syndrome
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- British Society for Dermatopathology
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- Metabolomic biomarkers in women with polycystic ovary syndrome: a pilot study
- Prediction of male-pattern baldness from genotypes
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Male-pattern baldness susceptibility locus at 20p11
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Congenital Adrenal Hyperplasia
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- From mechanisms to therapies: current advances breakthroughs in alopecia areata immunopathology
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle