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HLA-DRB5 and other genes may be linked to alopecia universalis.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

The study identified key genes that regulate the growth cycle of cashmere in goats, which could help improve breeding strategies.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

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.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Targeting a protein that blocks hair growth with microRNAs could lead to new hair loss treatments, but more research is needed.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

SOX9 is essential for the development of various organs and hair follicles.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Foxp3+ Regulatory T Cells are important for immunity and tolerance, affect hair growth and wound healing, and their dysfunction can contribute to obesity-related diseases and other health issues.

Melatonin makes cashmere grow earlier and more by increasing certain gene activity in goats.

K42 and K124 keratins are only found in horse hoof lamellae.

Ten miRNAs may play key roles in starting secondary hair follicle development in sheep foetuses.

Allopregnanolone changes gene expression in glioblastoma cells.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Researchers found genes linked to hair growth cycles in Inner Mongolia cashmere goats, which could help understand and treat hair loss.

Fusion proteins can protect hair from heat damage.

Overexpression of HDGF in melanocytes does not cause cancer.

Exosomes from fat-derived stem cells can potentially improve hair growth and could be a new treatment for immune-related hair loss.

Autophagy prevents early aging and maintains lipid and pheromone balance in mouse glands.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.