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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

The new method improves protein extraction and analysis in hair, aiding biomedical and forensic work.

A new method accurately measures minoxidil and finasteride in medicines.

New methods efficiently isolate dermal papilla cells from hair follicles, preserving their characteristics better than traditional methods.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Dried blood spots can be as stable as frozen liquid samples for storing certain metabolites.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Blocking TGFβ-RI signaling enhances surface ectoderm differentiation from human stem cells.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Forensic DNA phenotyping can now predict more physical traits and ancestry from DNA, but further improvements are needed.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

A new method was developed to accurately detect and measure 47 different drug ingredients in various products.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

Baicalin may help treat severe drug-induced skin reactions.

Researchers found a non-functional sheep keratin gene due to mutations.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

IL-1 blockade is effective for treating SURF, and personalized treatment is needed.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

A new compound from Royoporus badius activates immune cells and induces inflammatory responses.

Different PADI isoforms help cells develop diverse functions.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.