Search

everythinglearnresearchcommunity

for

Search:↓

Immunosuppressive and anti-TNF therapies in IBD patients can increase the risk of skin cancer and cause various skin issues.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

The document describes a woman with familial Parkinson's disease due to a genetic mutation, showing severe symptoms and poor response to treatment, and suggests finasteride may help reduce symptoms in Tourette syndrome.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

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

African American women have a higher risk of preterm delivery than Caucasian women, and inflammatory stimuli affect gene expression in cells related to PCOS, showing a heightened inflammatory state in women with PCOS.

Hair cortisol and cortisone levels may affect how work stress influences depression in Chinese fishermen.

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

The mutation helps mice handle heat better without affecting hair growth.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Human hair follicle stem cells show signs of low oxygen levels, which may be important for hair growth and preventing baldness.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Neoplasms hide in hair follicles to avoid the immune system.

Experts agree that PCOS affects women's health in complex ways, but more research is needed to understand and treat it effectively.

Certain mature cells in mouse lungs can turn back into stem cells to aid in tissue repair.

Alopecia areata is an autoimmune condition causing hair loss, influenced by genetics, stress, and diet, and may be prevented by a high soy oil diet.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Androgens can help prevent memory problems caused by apoE4.

New research suggests that skin cell renewal may not require a special type of cell previously thought to be essential.

Patients with certain skin symptoms and high ANA titers should be monitored for potential systemic lupus.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.