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Research 31–60 of 1000+
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hypotrichosis in a child with olmsted syndrome
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- The Genetics of Human Skin Disease
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Hair: more than just an appendage
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Woolly Antics between the Sheaths
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Androgenetic alopecia, hirsutism and hypertrichosis
- Learning from nudity: lessons from the nude phenotype
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Congenital atrichia and hypotrichosis