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Research 211–240 of 1000+
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Azithromycin and Roxithromycin define a new family of “senolytic” drugs that target senescent human fibroblasts
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- Pigmented Epithelioid Melanocytoma (PEM)/Animal Type Melanoma (ATM): Quest for an Origin. Report of One Unusual Case Indicating Follicular Origin and Another Arising in an Intradermal Nevus
- Specific In Vivo Ablation of Lrig1-Positive Follicular Progenitor Cells Results in Sebaceous Gland Loss in Mice
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- SPRY1 Deficiency in Keratinocytes Induces Follicular Melanocyte Stem Cell Migration to the Epidermis through p53/Stem Cell Factor/C-KIT Signaling
- Proliferation and differentiation of cultured human follicular keratinocytes are not influenced by biotin
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Proteome Analysis of Human Sebaceous Follicle Infundibula Extracted from Healthy and Acne-Affected Skin
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- The Dickkopf Protein Family in Non-Neoplastic Disorders: Emerging Roles and Therapeutic Targeting
- Spatiotemporal Expression Characterization of KRTAP6 Family Genes and Its Effect on Wool Traits
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- Chronic Alopecia
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Survival Skills for Doctors and their Families
- Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Molecular mechanisms of androgenetic alopecia
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- From a stem-cell–centered to a niche-centered view: the core role of collagen networks in hair loss and hair follicle miniaturization
- Role of skin microbiome and exosomes in Hair regeneration and disorders in diseases like Alopecia, Acne: A comprehensive review
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Adult female acne: Clinical and therapeutic particularities (Review)
- Itchy Black Hair Bristles on Back
- Hair Follicle Pigmentation
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Trichoscopic Findings in Androgenetic Alopecia