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A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Scientists improved an enzyme to better produce a hair growth-promoting chemical from an immunosuppressant.

Fatty acid transport protein 4 is essential for skin and hair development.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

OsUEV1B protein is essential for controlling phosphate levels in rice.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Sciellin is a protein that helps form protective layers in skin, hair, and nails.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Phospholipase A2 is necessary for the correct placement of PIN proteins in plant roots, affecting root growth.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

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

Sheep cells were successfully modified to include a spider silk protein gene.

Lysocellin helps stop cell damage from etoposide and may prevent hair loss.

Sesn2 protects inner ear hair cells from damage by regulating certain cell survival pathways.

A gene mutation causes woolly hair in a Syrian patient.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

A compound named ZCZ90 can increase muscle spindle firing, potentially helping treat muscle spasms and hypertension.

SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.