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THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Microneedle arrays with nanotechnology show promise for painless drug delivery through the skin but need more research on safety and effectiveness.

A new gene variant causes glucocorticoid resistance in a mother and son.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Disabling the FGF5 gene in sheep leads to longer wool.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

Many men misuse oral contraceptive pills for things like hair growth and muscle gain.

Self-assembling RADA16-I hydrogels with bioactive peptides significantly improve wound healing.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.