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Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

PCOS and related metabolic issues often run in families.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Phospholipase A2 enzymes play key roles in skin health and disease.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Extracts from three Polynesian plants were found to promote hair growth by affecting cell growth and gene expression related to hair.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Activating the Sonic hedgehog gene in mice can start the hair growth phase.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

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.

The meeting presented new findings on hair stem cells, pigmentation, genetics, and modern hair treatment techniques.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.