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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Mutations in the hairless protein gene cause hair loss.

Incidental prostate cancer was found in 4.89% of patients undergoing surgery for benign prostatic hyperplasia.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

A gene mutation causes monilethrix in a Chinese family.

Older age is the main risk factor for hemorrhagic cystitis after stem cell transplants.

Bisphenol-A (BPA) increases connections between brain cells and boosts their activity, but it blocks the effects of a male hormone on brain cell plasticity.

Sex steroids affect the MafB gene differently in male and female hamsters.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A woman with Budd-Chiari syndrome improved after treatment and needs a liver transplant, highlighting the importance of considering non-criteria antiphospholipid syndrome in similar cases.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.

Alcohol dependence affects stress hormone levels more than childhood maltreatment.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

Older age and prostatic hyperplasia in males increase the risk of hemorrhagic cystitis after stem cell transplantation.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.