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Research 331–360 of 1000+
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Symptoms Compatible With Long Coronavirus Disease (COVID) in Healthcare Workers With and Without Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection—Results of a Prospective Multicenter Cohort
- Central centrifugal cicatricial alopecia – an approach to diagnosis and management
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Study of gene expression alteration in male androgenetic alopecia: evidence of predominant molecular signalling pathways
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- <i>De novo</i> mutations in monilethrix
- Analysis of Sequences Controlling Tissue-Specific and Hyperproliferation-Related Keratin 6 Gene Expression in Transgenic Mice
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- The Genetics of Human Skin Disease
- Alopecia in Rhesus macaques correlates with immunophenotypic alterations in dermal inflammatory infiltrates consistent with hypersensitivity etiology
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Tricoscopia en la alopecia areata
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions
- Premature aging and cancer development in transgenic mice lacking functional CYLD
- Scalp biomarkers during dupilumab treatment support Th2 pathway pathogenicity in alopecia areata
- Iron Deficiency in Menstruating Adult Women: Much More than Anemia
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Frontal pseudoalopecia in history: Part 1—Fashionable forms
- Induction of T cell exhaustion by JAK1/3 inhibition in the treatment of alopecia areata
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Incidence of androgenic dermatologic side effects following placement of a levonorgestrel intrauterine device for menorrhagia: A survey-based study
- Three Cases of Alopecia Following Clinical Islet Transplantation
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Safety of skin care products during pregnancy.
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82