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Research 511–540 of 1000+
- Transcriptome Reveals Long Non-coding RNAs and mRNAs Involved in Primary Wool Follicle Induction in Carpet Sheep Fetal Skin
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Desmosomes in Developing Human Epidermis
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Molecular Mechanisms Regulating Hair Follicle Development
- In Ovo Injection of CHIR-99021 Promotes Feather Follicle Development via Modulating the Wnt Signaling Pathway and Transcriptome in Goose Embryos (Anser cygnoides)
- Premature Graying as a Consequence of Compromised Antioxidant Activity in Hair Bulb Melanocytes and Their Precursors
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- New developments in the molecular treatment of ichthyosis: review of the literature
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Fibrotic enzymes modulate wound‐induced skin tumorigenesis
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Role of regeneration in tissue repairing and therapies
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The microfollicle: a model of the human hair follicle for in vitro studies
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Examining the Effect of Notocactus ottonis Cold Vacuum Isolated Plant Cell Extract on Hair Growth in C57BL/6 Mice Using a Combination of Physiological and OMICS Analyses
- Inherited Disorders of the Hair
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Psoriasiform skin reaction due to Brazilian keratin treatment