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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A specific gene mutation causes long hair in Angora rabbits.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Selective breeding caused the unique curly hair in Mangalitza pigs.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Immune cells are essential for early hair and skin development and healing.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

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

New technologies help us better understand how skin microbes affect skin diseases.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

Researchers found 617 genes that behave differently in cashmere goat hair follicles, which could help understand hair growth.

Mange in rabbits is a serious disease that can spread to humans and is treated with medications and supportive care.