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Research 361–390 of 1000+
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Alopecia Areata
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Investigating self-reported hair loss following covid-19 infection in the Iraqi population
- Dermatological manifestations associated with pregnancy
- A New Immune-Biochemical Study To Identify Indicators Of The Response Of Infertile Polycystic Ovary Syndrome Patients To Metformin Treatment
- Pharma in the bedroom . . . and the kitchen. . . . The pharmaceuticalisation of daily life
- Niosomes as a propitious carrier for topical drug delivery
- Complications in Hair Restoration Surgery
- Developing the Concept of ‘Feel Ezzy Hair Oil’: Explore the Nature of Hair Oil with Respect to Personal Well-Being
- National scientific medical meeting 1996 abstracts
- Differential impact of environmental factors on systemic and localized autoimmunity
- Transforming growth factor-β in stem cells and tissue homeostasis
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Transcriptional Characteristics Showed That miR-144-y/FOXO3 Participates in Embryonic Skin and Feather Follicle Development in Zhedong White Goose
- Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report
- FOXN1 deficient nude severe combined immunodeficiency
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin