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Research 361–390 of 1000+
- Faculty Opinions recommendation of Hidradenitis suppurativa as a potential subtype of autoinflammatory keratinization disease.
- Management of a Refractory EIF3E-RSPO2 Fusion Positive Pilomatrical Cancer Patient with Encyclopedic Tumor Analysis Guided Treatment
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- The Molecular Pathogenesis of Trichilemmal Carcinoma
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Characterization of an autoimmune condition associated with AEC syndrome
- Inflammatory and non-melanocytic tumoral pathology of the nail
- Netherton Syndrome – Responding to Oral Retinoids
- IMPACT OF BIOMARKER IN PREDICATIVE TO RESPONSE ADJUVANT CHEMOTHERAPY AND OVERALL SURVIVAL IN FEMALES INFECTED WITH BREAST CANCER: A REVIEW ARTICLES
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Comparative ubiquitinomics of human skin reveals insulin receptor ubiquitination as a regulator of collagen secretion
- Comprehensive Administrative and Engineering Strategies for Radiation Protection and Occupational Health Safety
- Editorial: Inflammation, stem cells and wound healing in skin aging
- Review of Keratin Disorders
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Characterization of Human Keratin-Associated Protein 1 Family Members
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Building Epithelial Tissues from Skin Stem Cells
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11