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SIPHL1 from tomato enhances plants' response to low phosphate levels.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Deleting part of a gene in mice causes wavy hair and high pup loss.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

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

A new gene mutation causes a rare type of hair loss.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

Seven new genetic risk areas for prostate cancer were found.

Genetic variants in specific genes cause a type of hair loss.

A specific gene mutation causes severe skin and nail issues and hair loss.

Hair loss gene linked to prostate issues.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

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

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

DCPA is a chronic skin condition affecting the lower limbs, mainly in men, with unclear causes and treatments that often don't work well.

The Apc gene is crucial for normal skin and thymus development.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

SFRP2 boosts Wnt3a/β-catenin signals in hair growth cells, with stronger effects in beard cells than scalp cells.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.