Search

everythinglearnresearchcommunity

for

Search:↓

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

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

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

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

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Laminin-511 is essential for proper melanocyte movement and development in mice.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

KRT72 gene helps form hair.

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.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

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

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

DMBT1 and galectin-3 may help suppress epithelial skin cancer.

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

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

MCHR2 gene duplications may be linked to alopecia areata.

miR-214-3p helps nerve repair and recovery.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The rs1128977 gene variant may affect cholesterol and body measurements.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Found new possible treatments for hair loss.

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

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.