Search

everythinglearnresearchcommunity

for

Search:↓

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Ptprq has multiple forms that change during inner ear development.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

miR-199a-3p controls hair growth and is linked to alopecia areata.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

The research suggests immune system changes and specific gene expression may contribute to male hair loss, proposing potential new treatments.

Immune changes and specific genes contribute to male hair loss.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

The research found that different types of fibroblasts are involved in wound healing and that some blood cells can turn into fat cells during this process.

Fat cells help recruit healing cells and build skin structure during wound healing.

Hair follicle development and microbes help regulatory T cells gather in newborn skin.

Blocking JAK-STAT signaling can lead to hair growth.

Memory T cells in the skin balance staying put and moving into the blood, clustering around hair follicles, and increasing in number after infection.

The research identified various cell types in mouse and human teeth, which could help in developing dental regenerative treatments.

Newborn mouse skin cells can grow hair and this process can be recreated in adult cells to potentially help with hair loss.

Human hair follicles produce and respond to erythropoietin, helping protect against stress.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

New genes found linked to balding, may help develop future treatments.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.