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The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Cytokinins help Vitex negundo grow better and bloom more.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

Activating the hexosamine pathway can improve skin health and increase hair follicle stem cells.

Growth factors in skin increase with age, aiding development and healing.

Tofacitinib helped most teenagers in the study regrow hair with mild side effects.

A3B5 can reduce skin pigmentation and slow melanoma growth.

A new genetic mutation was found causing hair and eye issues in a boy.

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

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

A family medicine approach improves treatment and quality of life for children with enterobiosis.

Growing human skin cells in a 3D environment can stimulate new hair growth.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

A KLK5 inhibitor effectively improved skin symptoms in a mouse model of Netherton Syndrome.

Problem-based learning in a biology class improved students' thinking and problem-solving skills.

RACB in barley is crucial for cell polarity and nucleus positioning, aiding fungal infection.

Epidermal growth factor disrupts hair and gland formation in bandicoots.

Botryococcus braunii's three chemical races should be reclassified as separate species.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

AD-derived keratinocytes effectively mimic inflammation in atopic dermatitis.

Natubiotin is effective for treating different hair loss conditions when used with other therapies.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

Corneal health relies on cell migration and cooperation with the lacrimal gland, not Bmi1+ cells, and Eda gene mutations can cause dry eye disease.

Cell division orientation varies by body site and is linked to epidermal thickness and cell density.

EpiLife® media and younger donor age improve artificial skin model quality.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.