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Research 31–60 of 314
- Destruction of the arrector pili muscle and fat infiltration in androgenic alopecia
- Contaminants of emerging concern in the fetal environment
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- Multiomics global landscape of stemness-related gene clusters in adipose-derived mesenchymal stem cells
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- E-Poster
- 057 Single cell RNA and TCR sequencing reveals hyperexpansion of T cell clones and novel regulatory mechanisms of CD8+ T cells in murine alopcecia areata skin and draining lymph nodes
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Systemic Antifungals
- The Effect of Autologous Activated Platelet Rich Plasma (AA-PRP) Injection on Pattern Hair Loss: Clinical and Histomorphometric Evaluation
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Molecular Evolution and Protein Structure Variation of Dkk Family
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- WNT10B (wingless-type MMTV integration site family)
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Optimisation of Culture Conditions for Expansion of Human Epidermal Stem Cells
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- The Genetics of Human Skin Disease
- Comparison of allogeneic stem cell transplant conditioning regimens in AML, MDS and CLL
- SUMMARIES OF PAPERS