Search

everythinglearnresearchcommunity

for

Search:↓

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

More research is needed to understand how testosterone is maintained in adult males.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Certain gene variations might be linked to severe acne in women but not in men.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Spironolactone might lower the chance of getting rosacea.

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

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

Porphyra-334 may help reduce wrinkles and promote hair growth.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

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.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Blocking androgen activity in newborn rats affects body weight and appetite-related hormones differently in males and females.

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Understanding hair growth involves complex factors, and more research is needed to improve treatments for hair loss conditions.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.