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A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Claudin-1 is crucial for maintaining skin barrier and preventing inflammation.

Unique fat cells near fibrotic areas contribute to systemic sclerosis progression.

Changes in genes FGA, VWF, and ACTG1 may contribute to pemphigus vulgaris.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Multibranch carboxyl-modified cellulose is a safe and effective material for stopping bleeding.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

Schwann cell and M2 macrophage interactions contribute to keloid growth by increasing matrix deposition.

A man with skin and hair symptoms improved partially with specific treatment.

An infant developed excessive hair growth after a bone marrow transplant and cyclosporine treatment.

MOF controls skin development by regulating genes for mitochondria and cilia.

Collagen VII helps skin heal and stay strong, sirolimus may lower skin cancer risk in kidney transplant patients, high-molecular-mass hyaluronan helps naked mole rats resist cancer, dermal γδ T cells aid in hair growth in rodents, and overexpression of IL-33 in mouse skin causes itchiness, offering a model for studying allergic inflammation treatments.

The keratin network in mouse skin changes during cornification and affects the skin's protective barrier.

Understanding how acne develops in different diseases could lead to new treatments.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Mast cells might contribute to hair loss by causing skin thickening.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

Lymph vessels in airways vary by location, with the most in the upper pharynx and changes after birth.

Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Milia may come from the outer part of the hair follicle.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.