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Research 301–330 of 1000+
- Cutaneous signs in COVID ‐19 patients: A review
- Sex differences in COVID-19: the role of androgens in disease severity and progression
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- The CAP1/Prss8 catalytic triad is not involved in PAR2 activation and protease nexin‐1 (PN‐1) inhibition
- 5% Minoxidil topical foam on women: Menopause and other covariates
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Spiking dependence of SARS‐CoV‐2 pathogenicity on TMPRSS2
- The Involvement of RIPK1 in Alopecia Areata
- Involvement of RIPK1 in Alopecia Areata
- Leukokoria sebagai Tanda Peringatan Penyakit Coats dan Gangguan Retina Lainnya
- OXI1 kinase is necessary for oxidative burst-mediated signalling in Arabidopsis
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Matriptase-2, A Novel Suppressor of Hepcidin.
- Three cDNA sequences of mouse type I keratins. Cellular localization of the mRNAs in normal and hyperproliferative tissues.
- Akt2 and SGK3 are both determinants of postnatal hair follicle development
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- Correlation between changes of amino acid spectrum and alopecia in patients with obesity undergoing bariatric surgery: a prospective cohort study
- The role of phosphoglycerate dehydrogenase in cell proliferation and tumor progression
- Diagnosis dan Farmakoterapi Penyakit Paru Obstruktif Kronis
- Constitutive Internalization of the Leucine-rich G Protein-coupled Receptor-5 (LGR5) to the Trans-Golgi Network
- 5 alpha-reductase-2 gene mutations in the Dominican Republic.
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Roles of existing drug and drug targets for COVID-19 management
- Diverse origins of fibrinolytic enzymes: A comprehensive review
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- Perspective Chapter: Repurposing Natural Products to Target COVID-19 – Molecular Targets and New Avenues for Drug Discovery
- РОЛЬ ДЕРМАТОФИТОВ В ФОРМИРОВАНИИ СЕНСИБИЛИЗАЦИИ ОРГАНИЗМА
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats