Search
for
Sort by
Research 331–360 of 350
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The role of WNT10B in physiology and disease: A 10-year update
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Past, Present and Future Perspectives of Forensic Genetics
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Analogs of human genetic skin disease in domesticated animals
- Real-World Outcomes and Healthcare Utilization of Lanadelumab in Spain: Insights from First Cohort of Difficult-to-Treat Hereditary Angioedema Cases
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- RAGE and Its Ligands in Melanoma
- The Immunological Intersection of Psoriasis and Autoimmune Diseases: Shared Pathways and Clinical Implications
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Developmental Mapping of Hair Follicles in the Embryonic Stages of Cashmere Goats Using Proteomic and Metabolomic Construction
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- What does acne genetics teach us about disease pathogenesis?
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Genetic Basis of Male Pattern Baldness
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology