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Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Researchers found a non-functional sheep keratin gene due to mutations.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

A girl had rickets due to a gene mutation affecting vitamin D response.

PDRN helps repair tissue and improve wound healing with a high safety profile.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

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

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

KRTAP28-1 gene can help breed sheep with finer wool.

KRT72 gene helps form hair.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Prdm1 is necessary for early whisker development in mice but not for other hair, and its absence changes nerve and brain patterns related to whiskers.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Researchers found a genetic region that influences the number of coat layers in dogs.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.