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Researchers found four key proteins that affect the development of a specific hair type in Yangtze River Delta white goats.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Male pattern baldness may be caused by factors like poor blood circulation, scalp tension, stress, and hormonal imbalances, but the exact causes are still unclear.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Genetic variants affect minoxidil hair loss treatment success.

α-parvin is necessary for skin and hair growth and for the correct orientation of skin cells.

Akt2 protein is essential for normal cell division in early mouse embryos.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The document concludes that patients with skin of color need specialized dermatological care and education to manage unique skin conditions effectively.

Two mouse mutations cause similar hair loss despite different skin changes.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

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

No genetic link between prostaglandins and hair loss found.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Angora goat hair grows faster and produces more protein than cashmere goat hair, and certain hormones and nutrients positively affect hair growth and protein synthesis.