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Research 631–660 of 1000+
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Depressive and Anxiety Symptoms in Women with Polycystic Ovary Syndrome: A Meta-Analysis
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- New insights into the phenomenon of remissions and relapses in autoimmune diseases and the puzzle of benign autoantibodies in healthy individuals
- Evolution of long scalp hair in humans
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- In vitro strategies for mimicking dynamic cell–ECM reciprocity in 3D culture models
- Endocrinology
- Dutasteride reduces alcohol’s sedative effects in men in a human laboratory setting and reduces drinking in the natural environment
- Transposon control as a checkpoint for tissue regeneration
- Risk of autoimmune diseases in patients with RASopathies: systematic study of humoral and cellular immunity
- HDAC6-dependent deacetylation of NGF dictates its ubiquitination and maintains primordial follicle dormancy
- Peripheral patterns of calcitonin‐gene‐related peptide general somatic sensory innervation: Cutaneous and deep terminations
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- PLCD1 and Pilar Cysts
- Congenital cataract and slowly progressing facial skin lesions in a 5‐year‐old boy
- Clonal analysis of stem cells in differentiation and disease
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Deciphering gene regulatory programs in mouse embryonic skin through single-cell multiomics analysis
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Human skin color: Origin, variation and significance
- Gene-knockout mice with abnormal epidermal and hair follicular development