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Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

A new method makes analyzing large datasets with rare events faster and more efficient.

Molecular dynamics simulations help understand keratin's properties and predict hair's response to treatments.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

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

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Targeted protein degraders show promise in treating cancer but need to target more diverse proteins.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Deleting part of a gene in mice causes wavy hair and high pup loss.

The protein's size was reduced, but more work is needed to confirm its function.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Loss of Ten1 in mice causes telomere shortening and symptoms similar to human dyskeratosis congenita.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Two new gene mutations cause a rare hair disorder.

Proteolytic enzymes damage hair follicles by detaching stem cells.

New techniques helped identify rare wool proteins by reducing dominant ones.