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Research 121–150 of 1000+
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- The urine as a diagnostic key for a homozygous EGFR mutation
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- National scientific medical meeting 1996 abstracts
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- GAPO syndrome – Report of a rare case and review
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis.
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Clinical uses for calciotropic hormones 1,25-dihydroxyvitamin D3 and parathyroid hormone-related peptide in dermatology: a new perspective.
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- Männlicher Haarausfall – was uns unsere Gene verraten