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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Sheep cells were successfully modified to include a spider silk protein gene.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

GLI2 increases follistatin production in human skin cells.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Different fish use the same genes to regrow teeth.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Two new gene clusters important for hair formation were found on human chromosome 11.

Two new gene clusters important for hair formation were found on human chromosome 11.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Certain gene variations may increase the risk and severity of alopecia areata.

SOX4 is crucial for the development of melanoma.

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

Injecting specific oligonucleotides can change hair growth and structure by altering a gene.

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

Id2 gene helps keep hair follicle stem cells inactive.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Blocking SEPT4 might help heal wounds and regrow hair faster.

Hsc70 protein may influence hair growth by responding to androgens.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

The type of tumor suppressor gene lost affects the behavior of skin cancer.