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Research 391–420 of 1000+
- Ichthyosis
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Myotonic Dystrophy—A Progeroid Disease?
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Management of Androgenetic Alopecia
- Tabby pattern genetics – a whole new breed of cat
- Current Status of Hair Restoration Surgery
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Premature hair graying: a multifaceted phenomenon
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- Ulerythema Ophryogenes in a Saudi Male: A Case Report
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Interventions for androgenic alopecia in women
- Interventions for androgenic alopecia in women
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Lichen Planopilaris
- Hypotrichosis in a child with olmsted syndrome
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Biology of hair pigmentation and its role in premature canities
- The ATP sensitive potassium channel (KATP) is a novel target for migraine drug development
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice