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The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Cysteines in wool fibers are accessible and form important disulfide bonds.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

Collagen XVII is important for cell functions and its absence can worsen cancer outcomes.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

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

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

The model shows that filament flexibility and amino acid differences affect how fast intermediate filament proteins assemble.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Too much keratin 16 in mice skin causes abnormal skin thickening and structure.

Certain proteins help nerve cells branch, and other findings relate to cancer, stem cell behavior, and cell division.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.