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Research 901–930 of 1000+
- Increased PHGDH expression promotes aberrant melanin accumulation
- 307 Computer-assisted epitope prediction revealed potential autoantigens associated with human alopecia areata
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- 089 Neoplasms bypass immune evasion via hair follicle residence
- The TRF1 telomere protein is essential for the generation and maintenance of iPS cells and marks both pluripotent and adult stem cells
- In This Issue
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- JAK Inhibitors for Treatment of Alopecia Areata
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Apoptosis resistance in peripheral blood lymphocytes of alopecia areata patients
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Human skin color: Origin, variation and significance
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Heat treatment increases the incidence of alopecia areata in the C3H/HeJ mouse model
- Mommy — where do tumors come from?
- The common regulatory pathway of COVID-19 and multiple inflammatory diseases and the molecular mechanism of cepharanthine in the treatment of COVID-19
- Evaluation of the level of serum Interleukins (IL-2, IL-4, IL-15 andIL-17) and its relationship with disease severity in patients with alopecia areata
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia