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Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

The document concludes that insulin resistance is key in PCOS development and early treatment is crucial to prevent complications.

A specific gene change in APCDD1 increases the risk of hair loss.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Chicken feather growth involves specific genes and shares similarities with hair development.

Nonclassic 21-hydroxylase deficiency is a common, treatable genetic disorder causing reversible symptoms like acne and hair loss.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Genes and hormones cause hair loss, with four genes contributing equally.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Different genes are linked to various types of hair loss.

Male pattern baldness may be caused by scalp pressure on hair follicles, which increases with age and leads to a cycle of hair loss. This process is not directly determined by genes.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.