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Research 931–960 of 1000+
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- <i>Sept4/</i> ARTS Regulates Stem Cell Apoptosis and Skin Regeneration
- Generalised Glucocorticoid Resistance
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Dietary glucoraphanin prevents the onset of psychosis in the adult offspring after maternal immune activation
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Industry update: the latest developments in the field of therapeutic delivery, July 2018
- Alopecia Areata and Alopecia Areata Incognita
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Fibroblast heterogeneity and functions: insights from single-cell sequencing in wound healing, breast cancer, ovarian cancer and melanoma
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Ectopic Expression of a Truncated Isoform of Hair Keratin 81 in Breast Cancer Alters Biophysical Characteristics to Promote Metastatic Propensity
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice