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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A new gene mutation linked to a skin condition was found in a Spanish family.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Mutations in the KRT16 gene can cause skin and nail disorders.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

The hr gene is linked to hair loss in Valle del Belice sheep.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

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

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

TRPS1 is crucial for bone, kidney, and hair follicle development.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

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

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

A KRT32 gene variant causes loose anagen hair syndrome.

Defective nuclear transport may cause gene expression changes in Progeria.

Researchers found a new mutation causing total hair loss from birth.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Esrp1 is important for skin health by helping form and maintain the skin barrier.