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Research 241–270 of 519
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- GENETIC CONTROL OF CYTOKINES
- Clinical uses for calciotropic hormones 1,25-dihydroxyvitamin D3 and parathyroid hormone-related peptide in dermatology: a new perspective.
- Clinical Response to Combined Therapy of Cyclosporine and Prednisone
- A trichobezoar in a child with undiagnosed celiac disease: A case report
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Selection signatures for fiber production in commercial species: A review
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Cell Surface B2m-Free Human Leukocyte Antigen (HLA) Monomers and Dimers: Are They Neo-HLA Class and Proto-HLA?
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Frontal Fibrosing Alopecia and Reproductive Health: Assessing the Role of Sex Hormones in Disease Development
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Selective blockade of γc pathway ameliorates alopecia areata in a humanized murine model
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Quoi de neuf en recherche dermatologique ?
- Social selection favours offspring prone to the development of androgenetic alopecia.
- [Association of eight single nucleotide polymorphisms of chromosomes 20 and X with androgenetic alopecia among ethnic Han Chinese from Yunnan].
- Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data