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Certain inhibitors slow down plant growth by causing early cell specialization without changing the cell development pattern.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Msx2 and Foxn1 are both crucial for hair growth and health.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

A male with aromatase deficiency improved bone health with estradiol treatment.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

The 3D scaffold helped maintain hair cell traits and could improve hair loss treatments.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Girls with PCOS and menstrual disorders have notably higher androgen hormone levels.

Different types of polycystic ovary syndrome (PCOS) have varying severity, with Type I being the most severe and common.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Burn scars form abnormally due to changes in wound healing, and more research is needed to improve treatments.

A special bioink with nanoparticles helps regrow hair by reducing inflammation and promoting hair growth signals.

Cellular senescence has both cancer-blocking and cancer-promoting effects, and targeting senescent cells may improve health and lifespan.

A mouse gene mutation increases the risk of skin cancer.

Altering SSAT affects fat metabolism and body fat in mice.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

A rare benign skin tumor showed unusual features of sebaceous and sweat glands, important for correct diagnosis.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

The enzyme 25 Hydroxyvitamin D 1 α-Hydroxylase is essential for healthy skin and recovery after skin damage.