Related Experiment Video
Updated: Jun 24, 2025

05:48
A Behavioral Assay for Mechanosensation of MARCM-based Clones in Drosophila melanogaster
Published on: December 30, 2015
10.2K
Shedding more light on shedders
Piyamas Petcharoen1, Madison Nolan2, K Paul Kirkbride2
1School of Biology, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand.
Forensic Science International. Genetics
|June 8, 2024
Summary
This study on 100 individuals shows that human skin cell deposition is reproducible. Findings suggest that determining definitive "shedder status" is a continuum, not distinct categories.
Area of Science:
- Forensic science
- Human biology
- Biometrics
Background:
- Previous research on 11 donors suggested a continuum of shedder types.
- Reproducibility of cell staining for shedder status assessment in large populations was undetermined.
Purpose of the Study:
- To assess the reproducibility of cell staining for determining shedder status in 100 individuals.
- To investigate potential differences in cell deposition between sexes and hands.
- To analyze cell deposition over time post-handwashing.
Main Methods:
- 100 individuals tested for shedder status using DNA binding dye on thumbprints.
- Cell counts (cells/mm²) recorded at 220x magnification.
- Samples collected from both thumbs at multiple time points (0-180 min) post-handwashing, in triplicate, over three days.
Main Results:
- 98 out of 100 donors exhibited reproducible cell deposition.
- No significant difference in cell deposition between left and right thumbs in most cases.
- Males tended to deposit more cells than females.
- Many donors fell into intermediate categories when applying arbitrary boundaries for shedder status.
Conclusions:
- Human skin cell deposition is a reproducible phenomenon suitable for large-scale testing.
- Shedder status is best described as a continuum rather than discrete categories.
- Further research may refine shedder status determination and its forensic applications.
Related Concept Videos
Epistasis
46.7K
In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence phenotypes in a phenomenon called epistasis. For example, rabbit fur can be black or brown depending on whether the animal is homozygous dominant or heterozygous at a TYRP1 locus. However, if the rabbit is also homozygous recessive at a locus on the tyrosinase gene (TYR), it will have an unshaded coat that appears white, regardless of its TYRP1...
46.7K
Mechanism of Ciliary Motion
3.6K
The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
3.6K
Hedgehog Signaling Pathway
7.3K
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
7.3K
Replicative Cell Senescence
3.6K
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
3.6K
Restarting Stalled Replication Forks
5.8K
DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
5.8K
Incomplete Dominance
22.5K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.5K

