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Research 61–90 of 1000+
- Gsdma3 is required for hair follicle differentiation in mice
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Fatty acid oxidation fuels mitochondrial respiration to drive epidermal stem cell fate and differentiation
- Hair loss in children.
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- New clinico‐genetic classification of trichothiodystrophy
- The hair shaft: normality, abnormality, and genetics
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Scaling dermatosis in three dogs associated with abnormal sebaceous gland differentiation
- Trichothiodystrophy: Current Concepts
- Unravelling the threads of central centrifugal cicatricial alopecia
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Molecular Mechanisms Regulating Hair Follicle Development
- Markers of Epidermal Stem Cell Subpopulations in Adult Mammalian Skin
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Scalp whorls
- 4 Vitamin D resistance
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Book Reviews
- Practical Management of Hidradenitis Suppurativa