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Research 271–300 of 1000+
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Finding bald spots on chromosome 20p11
- Is polycystic ovary syndrome a sexual conflict? A review
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Identification and characterization of genes for skin and hair disorders
- Potential etiological factors in frontal fibrosing alopecia
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Clinical Snippets
- Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- Deletion of an Enhancer in FGF5 is Associated With Ectopic Expression in Goat Hair Follicles and the Cashmere Growth Phenotype
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study