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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Eyelid cells share signaling components but differ in pathway activity.

Dock5 is important for skin healing and could help treat diabetic wounds.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

iNKT cells help develop and maintain healthy skin in young mice.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Special gut cells help stem cells move to and fix injured areas by activating a specific signaling pathway.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.

A gene mutation causes monilethrix in a Chinese family.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Cathepsin E is crucial for normal skin cell differentiation and development.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Fibroblasts can be mistaken for neural cells, so functional validation is needed.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Skin needs dermal β-catenin activity for hair growth and skin cell multiplication.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Delta1 is crucial for controlling skin cell growth and preventing tumors in mice.

Mutations in the SNRPE gene cause hereditary hair loss.