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Research 61–90 of 1000+
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Androgenetic Alopecia in Men: An Update On Genetics
- Genetic and molecular aspects of androgenetic alopecia
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Manifestaciones dermatológicas en pacientes oncológicos pediátricos en un hospital de tercer nivel de Honduras
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Family History and Risk of Hair Loss
- <i>WNT10A</i> , dermatology and dentistry
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Is polycystic ovary syndrome a sexual conflict? A review
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients