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The skin protects the body, regulates temperature, senses touch, and makes vitamin D.

Fermentation of Finasteride with Ocimum sanctum L. creates new metabolite that inhibits tyrosinase.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Ovulation disorders are a major cause of infertility and menstrual problems in women.

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.

Reduced alpha smooth muscle actin may cause hair loss in androgenetic alopecia.

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

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 gene Prss53 affects hair shape and bone development in rabbits.

PCOS is a common hormonal disorder with symptoms like irregular periods and excess hair growth, managed with lifestyle changes and medications.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document recommends all three dermatology books for a library, noting their detailed content but also suggesting improvements in clarity and consistency.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

TGM3 is important for skin and hair structure and may help diagnose cancer.

AFM can diagnose hair disorders by revealing detailed hair surface changes.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

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

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

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

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Low zinc and selenium levels in sheep are linked to hair loss and thyroid problems.

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

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Progerin affects cell shape but not hair or skin in mice.