Search

everythinglearnresearchcommunity

for

Search:↓

Adding L-glutamine to the diet of Hanwoo steers may boost their immune system and help them cope with heat.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Lack of cystatin M/E causes thin hair and dry skin.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Haplogroup X found in Altaian population supports Amerindian origin.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

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

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

A patient with untreated congenital adrenal hyperplasia had large benign tumors in her adrenal glands removed, improving her symptoms.

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

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

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

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Nanoparticles improve drug delivery through the skin but more research is needed on their long-term effects and skin penetration challenges.

Keratose, derived from human hair, is a non-toxic biomaterial good for tissue regeneration and integrates well with body tissues.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

The study found that two enzymes linked to hair loss are located in different parts of the scalp, supporting a common treatment's effectiveness.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Costunolide may have multiple health benefits, including promoting hair growth and protecting against cancer and diabetes, but more research is needed.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

FOXN1 gene variants cause low T cells and immune issues from birth.

Phosphorylation of certain parts of the PIN3 protein is crucial for its role in plant root growth and response to gravity.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.