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A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

A new non-invasive method can analyze skin mRNA to understand skin diseases better.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Hair growth is influenced by hormones and goes through different phases; androgens can both promote and inhibit hair growth depending on the body area.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

MC4R gene variants not linked to female hair loss.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Certain gene variations are linked to better memory in healthy Chinese women.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

Certain genes are more active in baby scalp cells and can help grow hair when added to adult mouse skin cells.

Caffeine improves hair growth, thickness, and reduces shedding.

AGA treatments like minoxidil and LLLLT are safe and effective for gender minority patients.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

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.

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.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

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

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

A genetic marker linked to a type of hair loss was found in most patients studied.

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