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Research 31–60 of 1000+
- Hair loss in children.
- [Visual field defect in a patient given sodium valporate then carbamazepine: possible effect of aminotransferase inhibition].
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- The genetic basis of dermatophytosis skin infection susceptibility
- The hair shaft: normality, abnormality, and genetics
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Characterization of an autoimmune condition associated with AEC syndrome
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- ABC of Dermatology: Diseases of the hair and scalp
- Australian Hair and Wool Research Society Cutaneous Biology and Endocrinology Workshop
- Low prevalence of twisted hair in anorexia nervosa
- Molecular Mechanisms Regulating Hair Follicle Development
- Uncombable hair syndrome and beyond
- HAIR AND SYSTEMATIC DISEASE
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- AN UPDATE OF HAIR SHAFT DISORDERS
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Open questions in hidradenitis suppurativa research: a hair biologist's perspective
- Transcriptomic crossroads: Decoding genes and pathways that connect alopecia areata with chronic inflammatory skin disorders
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- 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
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia