Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The improved genome of the African spiny mouse helps study its tissue regeneration.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

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

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

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

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

A rare genetic mutation in the EGFR gene caused severe skin issues and other health problems in a Slovakian girl, who is now 4 years old and receiving care.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A new DSG4 gene mutation causes hair defects in a young girl.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Researchers cloned a gene from Xinjiang fine-wool sheep, finding it very similar to other sheep and somewhat similar to goats, humans, and rabbits.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

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

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

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

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.