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Research 211–240 of 1000+
- AVALIAÇÃO DA CRIPTOSPORIDIOSE EM CÃES E SUAS IMPLICAÇÕES NA SAÚDE ÚNICA
- Efectos de la alteración de los niveles de allopregnanolona durante periodos críticos del neurodesarrollo en la vulnerabilidad al consumo de alcohol
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Depletion of S100A4+ stromal cells results in abnormal nipple development and nursing failure
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- DHEA and TNF-α: Key Factors in Managing Polycystic Ovary Syndrome in Iraqi Females
- Generation of an integration-free human induced pluripotent stem cell line MUSIi010-A from occipital scalp fibroblasts of a male patient with androgenetic alopecia
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Gene expression of type 2 17β hydroxysteroid dehydrogenase in scalp hairs of hirsute women
- Polyclonal origin and hair induction ability of dermal papillae in neonatal and adult mouse back skin
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- The Potential Relevance of the Microbiome to Hair Physiology and Regeneration: The Emerging Role of Metagenomics
- Biotinidase deficiency characterized by skin and hair findings
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- CD201+ fascia progenitors choreograph injury repair
- Development and Molecular Characterization of Human Placental Mesenchymal Stem Cells from Human Aborted Fetal Tissue as a Model to Study Mechanism of Spontaneous Abortion
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- 316 Specialized ribosomes in human dermal fibroblast senescence
- 313 Different polyamine levels in the vertex and occipital hair of pattern hair loss patients
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Assessment of the impact of VDR polymorphisms on selected hormonal, metabolic and mineral balance markers in young women with hyperandrogenism
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- 9. Immunology and Genetics