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

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

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

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Certain gene variations may increase the risk of hair loss in Egyptians.

Identified genes linked to male-pattern baldness may help develop new treatments.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

The model accurately predicts age from saliva and buccal cells for forensic use.

The study found key factors in the cause of hidradenitis suppurativa, its link to other diseases, and identified existing drugs that could potentially treat it.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Allopregnanolone changes gene expression in glioblastoma cells.

Essential oils from Hedychium spicatum have potential for developing natural drugs with pain-blocking, fever-reducing, anti-inflammatory, and antioxidant properties.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Mice with alopecia areata had wider lymphatic vessels in their skin.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Targeting specific genes in certain pathways may help treat male pattern baldness.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Scientists can use engineered microbes to make L-aspartate and related chemicals, but there's still room to improve their efficiency.

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.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.

Six genetic conditions are often linked to complete scalp hair loss in children.

Oral and topical finasteride are effective and safe for treating female hair loss.