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Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Fetal-maternal stem cells in a mother's hair can help with tissue repair and regeneration long after childbirth.

The patient with total hair loss did not regrow hair despite treatment, indicating a poor outlook for this type of hair loss.

The Drug Ontology was updated to better classify drugs for hypertension, malaria, and opioid abuse, and to allow for more accurate research queries.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

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.

Androgens can cause hair growth in some areas and hair loss on the scalp.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

MC4R gene variants not linked to female hair loss.

The E2 protein affects gene activity in hair follicles of mice.

Blocking 5α-reductase can harm memory and brain structure, and increase harmful brain changes in male mice used for Alzheimer's disease research.

Different populations have distinct hair structures related to their ancestry.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

No link found between specific genes and female pattern hair loss.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.