Search
for
Sort by
Research 181–210 of 1000+
- Hair, Hormones, and High-Risk Prostate Cancer
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Congenital hair loss disorders: Rare, but not too rare
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- An epidemiological study of androgenic alopecia in 3114 Korean patients
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Prevalence and treatment of Alopecia areata in Taif area, KSA
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Non-nutritional rickets: Approach, precision medicine, and outcomes
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- The Review on Alopecia Areata : A Comprehensive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- Barbering in Laboratory Rodents: Problems and Prospects
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Genetic factors in the etiology of intervertebral disc herniation and protrusion
- Análise dos níveis de metilação e de polimorfismos genéticos dos genes GSTP1, MGMT, VDR e AR em pacientes com câncer de próstata
- Navigating Diagnostic Uncertainty: Frontal Fibrosing Alopecia Versus Keratosis Pilaris Atrophicans Faciei With Genetic Testing Insights
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report