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Research 181–210 of 1000+
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Female-patterned alopecia in teenage brothers with unusual histologic features
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data
- 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study
- Common contact allergens implicated in frontal fibrosing alopecia found in over-the-counter hair growth serums and solutions
- Production of a 135-residue long N-truncated human keratinocyte growth factor 1 in Escherichia coli
- NEDD4 Transcript Variant 3 and IGF-1 as Molecular Markers in the Development and Prognosis of Keloids
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Common Skin Disorders in Pediatric Skin of Color
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- A comedonal variant of chronic cutaneous lupus erythematosus: Case report and literature review
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Drug interactions between common dermatological medications and the oral anti-COVID-19 agents nirmatrelvir-ritonavir and molnupiravir
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Common Skin Diseases and Metabolic Syndrome: A Proinflammatory Chemokine Perspective
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Tissue Retinol‐Binding Protein 4 Expression and Its Genetic Variants (rs3758539) in Patients With Severe and Treatment‐Refractory Alopecia Areata: Association With Response to Baricitinib
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter