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

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

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

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.

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

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

Dermal EZH2 controls skin cell development and hair growth in mice.

Women with hair loss have more androgen receptors in certain hair follicles.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

Updated treatments for female hair loss include minoxidil, antiandrogens, hair transplants, and light therapy.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Minoxidil might cause blood vessel-related skin lesions when applied to the scalp.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Dermal papilla cells are key for hair growth and color, influencing hair type and size, and their interaction with stem cells could help treat hair loss and color disorders.

Skin reactions are a common reason for emergency visits due to drug allergies, with some severe cases needing intensive care.