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Research 181–210 of 193
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Screening and expression validation of key proteins for secondary hair follicle growth in cashmere goats based on iTRAQ quantitative proteomics technology
- Dynamics of Actin Filaments Play an Important Role in Root Hair Growth under Low Potassium Stress in Arabidopsis thaliana
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- CCDC22 and CCDC93, two potential retriever-interacting proteins, are required for root and root hair growth in Arabidopsis
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Congenital Adrenal Hyperplasia
- Fleece traits and important physical properties of hair fibers in lori goats.
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Cutaneous signals of immune system disease
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- <i>WNT10A</i> , dermatology and dentistry
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy