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A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

The KRTAP36-2 gene in sheep affects wool yield.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A gene variation is linked to hair thickness in Asians.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

PCOS in women from Karnataka is influenced by genetics, family history, and insulin resistance, requiring better diagnosis and treatment.

The K15 promoter effectively targets stem cells in the hair follicle bulge.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

The N-K GM Series offers highly selective, eco-friendly medicines targeting harmful microbes, free for personal use.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

Two siblings have a rare hair condition caused by a new genetic variant.

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

A stable, active version of a growth factor was made in bacteria, showing promise for medical use.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

Microbial communities in Duku plant roots vary between wet and dry habitats, affecting plant health.

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

Variation in the TCHH gene affects wool curliness in sheep.