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Research 61–90 of 92
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Genetic Hair Disorders: A Review
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Alopezien und Hypotrichosen im Kindesalter
- Claves diagnósticas en displasias pilosas II
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Current Genetics in Hair Diseases
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Lrig1-expressing epidermal progenitors require SCD1 to maintain the dermal papilla niche
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Molecular Genetics of Human Hair Diseases
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Implication of microRNA regulation in para-phenylenediamine-induced cell death and senescence in normal human hair dermal papilla cells
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Integrative Analysis of the Metabolome and Transcriptome Reveals the Mechanism Underlying Differences in Skin Development Between the New Zealand Rabbit and the Rex Rabbit
- Novel Insights into TSC22D Family Genes in Metabolic Diseases and Cancer
- PIEZO1-mediated calcium signaling reinforces mechanical properties of hair follicle stem cells to promote quiescence
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations