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Research 151–180 of 1000+
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Genetic hair and nail disorders
- Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Hair Shaft Disorders
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Hair Follicle Development in Mouse Pluripotent Stem Cell-Derived Skin Organoids
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Cronkhite-Canada syndrome: A case report and literature review
- Reptile scale paradigm: Evo-Devo, pattern formation and regeneration
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- The developmental basis of fingerprint pattern formation and variation
- Skin Development and Disease: A Molecular Perspective
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Direct Reprograming of Mouse Fibroblasts into Dermal Papilla Cells via Small Molecules
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Genome-Wide Identification and Characterization of the Wnt Gene Family in Donkey (Equus asinus): Phylogenetic Analysis and Expression Profiling
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Advances in Bioprinting to Model Immune‐Mediated Skin Diseases
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Temporal Triangular Alopecia – A Diagnostic Dilemma: Case Series of Six Patients
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- EMT Factors and Metabolic Pathways in Cancer
- Anatomy and Physiology of the Skin