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Research 511–540 of 1000+
- Poster Abstracts
- Syndromes of Severe Insulin Resistance (SSIRs)
- Cutaneous manifestations of systemic infection in children
- Dermatoses of pregnancy
- Small molecules and small molecule drugs in regenerative medicine
- Mitoxantrone
- An Update on Drug-Induced Pigmentation
- Lupus erythematosus: considerations about clinical, cutaneous and therapeutic aspects
- Emerging smart microneedle technologies in psoriasis: convergence of nanocarriers, machine learning, and personalized delivery
- Microinfusão de metotrexato nas lesões de couro cabeludo podem auxiliar no alívio da alopécia frontal fibrosante?
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- The role of hair follicles and Edar signalling in cutaneous wound healing
- How to diagnose a lipodystrophy syndrome
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Polygenic risk score predicting susceptibility and outcome of benign prostatic hyperplasia in the Han Chinese
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Minoxidil may suppress androgen receptor-related functions
- Potential use of human hair shaft keratin peptide signatures to distinguish gender and ethnicity
- Chronic overlapping pain conditions and nociplastic pain
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Androgenetic Alopecia in Men: An Update On Genetics
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA