Search
for
Sort by
Research 30 of 1000+
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Demethylation of ITGAV accelerates osteogenic differentiation in a blast-induced heterotopic ossification in vitro cell culture model
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- A Simple Method to Extract DNA from Hair Shafts Using Enzymatic Laundry Powder
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- British Society for Dermatopathology
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- Introduction to Transplantology
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- What do we know about osteoma cutis? Literature review. Clinical cases
- Past, Present and Future Perspectives of Forensic Genetics
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Madarosis from mitochondriopathy
- E-Poster
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- POINT OF CARE W RADIOLOGII
- Paint brush hair: a case report
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.
- Twelve‐point scale grading system of scanning electron microscopic examination to investigate subtle changes in damaged hair surface
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Evaluation method of the degree of hair damage. (I). Measurement of tensile strength of human hair by "the multi-point tension test method".
- Time Point 1 and 2 of Hair Cortisol
- 41 Temporal point (TP)Recreating the Temporal Points