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Research 421–450 of 1000+
- Congenital atrichia with papular lesions
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Eyes open on stem cells
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Diseases of Hair
- A Comprehensive Review of GWASs of Human Hair Traits
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Diseases of Hair
- "Preparation and Physicochemical Characterization of Topical Niosomal Formulation of Minoxidil and Tretinoin"
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Bioengineered skin organoids: from development to applications
- Editor's evaluation: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A new type of pachyonychia congenita.
- Genetic hair and nail disorders
- Ectodermal Dysplasia: Variable Expressions
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation
- Clouston’s syndrome: a rare case report
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1