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Research 481–510 of 1000+
- Molecular characterization, expression and methylation status analysis of BMP4 gene in skin tissue of Liaoning cashmere goat during hair follicle cycle
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Retinoids Putting the “A” in Alopecia
- Tracing Recombinant Bovine Somatotropin Ab(Use) Through Gene Expression in Blood, Hair Follicles, and Milk Somatic Cells: A Matrix Comparison
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- BH02 Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with the <i>AIRE</i> gene mutation treated with ruxolitinib
- Gene Editing Technologies in Aesthetic Dermatology—Mechanisms, Emerging Applications, and Patient Safety Paradigms
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Correlation between Androgenetic Alopecia and Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Variant Infection in China
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank
- Serum interleukin-37 and its gene polymorphism (rs3811047) in Egyptian patients with alopecia areata
- Frequency of an electrophoretic variant of hair alpha keratin in human populations.
- The Rotterdam Study: 2016 objectives and design update
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Recent advances in the genetics of alopecia areata
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata
- ATP-dependent chromatin remodeling during mammalian development
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men