Search

everythinglearnresearchcommunity

for

Search:↓

Telogen Effluvium is a condition causing excessive hair loss due to stress, illness, drugs, or hormonal changes, and can be treated with specific products or naturally resolves after 3-4 years.

Stem cell therapy is promising for treating various health conditions, but more research is needed to understand its full potential and address challenges.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Different body areas in mice produce different hair types due to interactions between skin layers.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

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

Wearing a hijab changes the common bacteria and fungi on the scalp, possibly affecting skin health.

Growth factors-rich plasma treatments can significantly speed up wound healing and tissue regeneration.

The Shen Bai Hair Growing Decoction may help treat hair loss by promoting hair growth and reducing inflammation.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

Epithelial stem cells are crucial for tissue renewal and repair, and understanding them could improve treatments for damage and cancer.

Finasteride affects alcohol intake in male mice, possibly due to neurosteroids.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Activating β-catenin increases melanocytes and decreases Schwann cells.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Whale genes show changes that help them live in water, like less hair and better flippers.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A new gene variant causes glucocorticoid resistance in a mother and son.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.