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

No clear link between specific gene and hair loss in Mexican brothers.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Using the drugs AMD3100 and Tacrolimus together greatly improves skin healing and hair growth after a deep skin cut by increasing stem cells in the wound.

Disabling the FGF5 gene in sheep leads to longer wool.

A device was made in 2008 to measure hair loss severity. Other findings include: frizzy mutation in mice isn't related to Fgfr2, C/EBPx marks preadipocytes, Cyclosporin A speeds up hair growth in mice, blocking plasmin and metalloproteinases hinders healing, hyperbaric oxygen helps ischemic wound healing, amniotic membranes heal wounds better than polyurethane foam, rhVEGF165 from a fibrin matrix improves tissue flap viability and induces VEGF-R2 expression, and bFGF enhances wound healing and reduces scarring in rabbits.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

The CORIN gene variant causes the golden color in Siberian cats.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

Three genes linked to the development of trichilemmal cysts were found.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Using special RNA to target a mutant gene fixed hair problems in mice.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

The balance between androgen receptor and p53 is crucial for sebaceous gland differentiation.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Skin problems like itching, dry skin, and hair loss are more common in hepatitis C patients after interferon treatment, but lichen planus is not linked to the infection.

Hepatitis C virus can cause skin diseases and dermatologists play a crucial role in identifying these conditions.

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

The authors maintain that shorter androgen receptor alleles may lead to milder COVID-19 by positively affecting the immune response, not due to changes in testosterone levels or activity.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

A new gene mutation causes insulin resistance in a girl and her mother.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.