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Research 31–60 of 112
- Inherited Disorders of the Hair
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Enanthem in Patients With COVID-19 and Skin Rash
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Genetics of Structural Hair Disorders
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Botanical extracts in combination improve autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations
- Congenital Atrichia: A Case Report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Molecular Genetics of Human Hair Diseases
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Advances in Hair Diseases
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Genetic Hair Disorders: A Review
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Alopezien und Hypotrichosen im Kindesalter