Search

everythinglearnresearchcommunity

for

Search:↓

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.

New treatments for prostate cancer are less toxic and show promise, but more research is needed to enhance their effectiveness and reduce side effects.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

CDP is crucial for lung and hair follicle cell development.

Potassium channel openers are effective in treating heart conditions, high blood pressure, pulmonary diseases, bladder issues, and hair loss, but more selective drugs are needed.

Both mouse and rat models are effective for testing alopecia areata treatments.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Explosions don't stop hair proteins from being used to identify people.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Melatonin receptors in hair follicles help regulate hair growth and could treat hair loss.

Chicken feather gene mutation helps understand human hair disorders.

Iron deficiency might contribute to hair loss in women.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

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

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Hair follicle development and microbes help regulatory T cells gather in newborn skin.

New targets for making and using brain-synthesized steroids could lead to better treatments for brain disorders and alcoholism.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Growth factors are crucial for hair development and could help treat hair diseases.

Versican, a protein, is less present in thinning hair follicles and this decrease might contribute to common hair loss in men.

Lower levels of certain brain chemicals are linked to worse PTSD symptoms in men.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.