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Certain groups may need vitamin supplements to improve hair health and prevent other health problems.

Loose Anagen Hair Syndrome is a hereditary condition causing hair loss in children due to abnormal hair follicles.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The gene Prss53 affects hair shape and bone development in rabbits.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

The document concludes that treating female hair loss should target reducing excess androgen and blocking its effects on hair follicles, with the best treatments being hormonal therapy, adrenal suppression, and topical minoxidil.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

The document suggests that nerve issues might contribute to hair loss and that testing sensation could predict these nerve problems.

Key genes linked to hair growth and cancer were identified in hairless mice.

Prolactin affects the production of different keratins in human hair, which could lead to new treatments for skin and hair disorders.

Edar signaling is crucial for controlling hair growth and regression.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

EGFR helps control how hair grows and forms without needing p53 protein.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

pCLCA2 protein may help maintain skin structure and function.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

The Notch signaling pathway is important for hair follicle development and could help create treatments for hair disorders.

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.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.