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Research 31–60 of 1000+
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Who Am I? Eyebrow Follicles Minimize Donor-Derived DNA for Germline Testing After Hematopoietic Stem Cell Transplantation
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- Congenital Atrichia: A Case Report
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Exploring Nanotechnology With Traditional Herbal Pharmacology: Nano Carrier-Based Phytochemical Delivery In PCOS Treatment
- Testing Chemotherapeutic Agents in the Feather Follicle Identifies a Selective Blockade of Cell Proliferation and a Key Role for Sonic Hedgehog Signaling in Chemotherapy-Induced Tissue Damage
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Is hormone testing worthwhile in patients with female pattern hair loss?
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- scMC learns biological variation through the alignment of multiple single-cell genomics datasets
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Tracking research trends and hotspots in sperm DNA fragmentation testing for the evaluation of male infertility: a scientometric analysis
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Genetic Hair Disorders: A Review
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Artificial Intelligence in Aesthetic Medicine: Applications, Challenges, and Future Directions