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Research 31–60 of 1000+
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Short anagen hair syndrome
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Biology and Genetics of Hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Dermatopathology and molecular genetics
- Disorders of hair in children
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Current Genetics in Hair Diseases
- Genetics of Alopecia
- Fibroblast bioelectric signaling drives hair growth
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Diseases of Periocular Hair
- Hair and scalp disorders