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Research 481–510 of 1000+
- Breaking the biofilm- A persistent case of deep pyoderma in a Bullykutta dog
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep
- Lichen Planopilaris As Part of Multiple Autoimmune Syndrome: A Case Report of New Association
- Subject Index
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- The Role of Propioni Bacterium acnes in Acne Vulgaris
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Australasian Society for Dermatology Research Meeting, May 2007
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- Supplementary Methods, Tables 1-2 and Figures from Tumor Stroma–Derived Wnt5a Induces Differentiation of Basal Cell Carcinoma of <i>Ptch</i>-Mutant Mice via CaMKII
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Temporal expression and steroidal regulation of piRNA pathway genes (mael, piwi, vasa) during Silurana (Xenopus) tropicalis embryogenesis and early larval development
- NUDT15 R139C-related thiopurine leukocytopenia is mediated by 6-thioguanine nucleotide-independent mechanism in Japanese patients with inflammatory bowel disease
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Association study between the -866G/A polymorphism in the promoter of uncoupling protein-2 gene and polycystic ovary syndrome
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function
- The association of cytosine-adenine-guanine repeat polymorphism in the androgen receptor gene with nodulocystic acne in Egyptian patients
- Review of Different DNA Extraction Methods in Hair Shafts
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Mechanisms of aluminium toxicity, tolerance and amelioration in wheat
- Clinical Profile of Patchy Alopecia: Report from a Tertiary Care Hospital of Bangladesh
- Psoroptosis of sheep and wild goats: clinical manifestation and treatment under anthropobiocenosis
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans