Search

everythinglearnresearchcommunity

for

Search:↓

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A gene variation is linked to hair thickness in Asians.

Long-lived proteins may predict age-related diseases.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

miR-144 affects hair growth by interacting with Lhx2.

Intralesional chemotherapy with 5-fluorouracil and methotrexate may worsen keratoacanthoma-type skin cancer in transplant patients.

A new change in the WNT10A gene caused a condition leading to short hair growth in a Chinese family.

Nephronectin is linked to worse breast cancer outcomes and helps cancer spread.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

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

MIR135b affects wound healing by targeting genes, and PDRN may help heal wounds by altering this pathway.

miRNA-211 reduces melanin in Cashmere goats by suppressing AP1S2.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

A new DSG4 gene mutation causes hair defects in a young girl.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

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

LL-37 helps stem cells grow and move, aiding tissue regeneration and hair growth.

FOXN1 gene variants cause low T cells and immune issues from birth.

Mutations in the LIPH gene cause woolly hair in a child.

lncRNA VIM-AS1 helps heal diabetic wounds by boosting energy production and reducing cell aging.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Phospholipase C-δ1 is crucial for normal hair development.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.