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

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

Sickle cell disease affects BMI and pain frequency, with HbSS patients having more pain and unhealthy BMI.

Overexpressing AVP1 and AtNHX1 in plants improves salt tolerance and root hair development.

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

Transglutaminase 2 may control sebocyte maturation and lipid metabolism.

Trans-esophageal echocardiography is crucial for accurately diagnosing heart issues in lupus patients.

Fish scale collagen peptide speeds up wound healing effectively.

The SGAP flap effectively treats large sacral pressure sores with good results and minimal complications.

Steroid sulfatase inhibitors could potentially treat hormone-related disorders like certain cancers, hair loss, acne, and improve cognitive dysfunction.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

SCD1 is crucial for skin health and overall energy balance.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

The composite sponge helps heal diabetic wounds by reducing inflammation and promoting new blood vessel growth.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

A woman with severe hair loss due to systemic sclerosis regrew her hair in 4 months using a combination of treatments.

SK2 channels help control sensory signals in rat muscle spindles and hair follicles.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Sebaceous lipids are crucial for keeping skin and eyes healthy in mice.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

A specific gene mutation causes sparse, brittle hair in a family.

Adipose stem cell-derived exosomes may improve hair count and scalp health, potentially outperforming current treatments like minoxidil.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Human hair follicles can be used to create stem cells that might help clone hair for treating hair loss or helping burn patients.