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A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Epidermal stem cells don't use gap junctions to communicate.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

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

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Found new possible treatments for hair loss.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

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

A man with KID syndrome developed a rare cancer in a long-term skin infection.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Finasteride treatment changes Cx43 in rat testes, possibly causing fertility issues.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

PAON shows skin patterns due to genetic mosaicism.

The study identified unique genes in hair follicle cells and their environment, suggesting these genes help organize cells for hair growth.

The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Activating Nrf2 can help protect against hearing loss.