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Research 181–210 of 1000+
- Mutant Cx43 in Skin Differentiation and Disease
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Genetics of Structural Hair Disorders
- Segmental Vitiligo and Hair Curling After Interferon α and Ribavirin Treatment for Hepatitis C
- Hair Manifestations of Systemic Disease
- The Comparison of Metabolic Syndrome Parameters, Trichoscopic and Trichoscan Characteristics in Androgenetic Alopecia (AGA) and Early-Onset Androgenetic Alopecia (Early-Onset AGA)
- Uncombable hair in a case of Zellweger syndrome – A new association
- Nutrition and hair
- Platelets rich plasma versus minoxidil 5% in treatment of alopecia areata: A trichoscopic evaluation
- A girl struggling with extremely unruly hair
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Generalized Hypertrichosis Due to Topical Minoxidil
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Traumatic panniculitis with hypertrichosis
- The Shaven (Sha) Mutation, Chromosome 15
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Clinical Snippets
- Alopecia and Thyroid Disease
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Impaired metabolic effects of metformin in men with early-onset androgenic alopecia
- Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- PNEUMONIA AND DEMODICOSIS IN CROSSBREED POMERANIAN