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Research 91–120 of 1000+
- Hair and Scalp Diseases
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- 0961 Exploring mitochondrial dysfunction in miniaturized hair follicles: Insights into androgenetic alopecia
- Normal Ultrasound Anatomy of the Skin, Nail, and Hair
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Hypomyelinating leukodystrophy-10 presenting with an additional atypical feature of increased body hair and Mongolian spots
- Vitamins and Alopecia
- Growth Factors and Cutaneous Pathology
- Development and homeostasis of the sebaceous gland
- Clinical Snippets
- Mutant Cx43 in Skin Differentiation and Disease
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Double mutation of <i>claudin‐1</i> and <i>claudin‐3</i> causes alopecia in infant mice
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- The Shaven (Sha) Mutation, Chromosome 15
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Bariatric Surgery and Its Effects on the Skin and Skin Diseases
- A Review on-Types and Treatment of Alopecia
- Remarkable Improvement of Nail Changes in Alopecia Areata Universalis with 10 Months of Treatment with Tofacitinib: A Case Report
- <i>WNT10A</i> , dermatology and dentistry
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Clinical Corner: Case Report Spermatozoa and Chronic Treatment with Finasteride: A TEM and FISH Study
- Pathological Feature and Expression of Androgen Receptor in Affected Area of Androgenetic Alopecia in Various Syndromes of Traditional Chinese Medicine
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- A Case of Hair Structure Abnormality Associated with Iron Deficiency Anaemia