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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Targeting specific cell interactions may help treat skin fibrosis.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Lack of TG2 increases fat storage and lowers cell cleanup in skin oil cells.

Disrupting Bcl-xL in mice reduces skin cancer risk.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

TGFβ's manipulation of inflammation and immune cells affects cancer spread, suggesting new treatment strategies and biomarkers.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Smad2 and Smad3 are essential for normal skin development, and their absence causes severe skin issues and cancer.

LncRNAs may help improve brain cancer treatment and diagnosis.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Immune system changes may contribute to female pattern hair loss.

New cancer treatments show promise in reducing tumor growth and improving skin regeneration in mice.

A new method quickly detects hair changes from EGFR inhibitors using a microscope.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

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

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Snail2 is crucial for hair growth and affects skin cancer development.

A new genetic mutation was found causing hair and eye issues in a boy.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

No link found between new male baldness genes and female hair loss.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.