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

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Improving artificial vascular grafts requires better materials and surface designs to reduce blood clotting and support blood vessel cell growth.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

The document concludes that accurate diagnosis of male and female gonadal disorders is crucial for effective treatment and better patient outcomes.

Drug repurposing shows promise for treating many medical conditions.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

There are various effective hormone treatments for puberty induction in boys and girls with hypogonadism, and starting treatment early is important.

New hair follicles could be created to treat hair loss.

Some skin tumors may start from hair follicle stem cells.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

The study identified 12 potential biomarkers for hair loss and how they affect hair growth.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Skin cysts might help advance stem cell treatments to repair skin.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Enzymes called 5α-reductases have many body functions and need more research to safely use inhibitors.

Coffee bean residue extract helps hair growth by activating cell processes.

A new method using a microfluidic device can prepare hair follicle germs efficiently for potential use in hair loss treatments.