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Research 301–330 of 1000+
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- The molecular basis of human keratin disorders
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- “Degeneration” in Dermatopathology
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Kaposi varicelliform eruption
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Vitamin D and the Skin: A Review for Dermatologists
- Off-label uses of retinoids in dermatology
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Trichoscopy in genetic hair shaft abnormalities
- Eyebrow Loss
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Hair Keratin
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children