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Auxin and ethylene hormones both work together and against each other to control plant growth.

Fat tissue-derived cells show promise for repairing body tissues, but more research and regulation are needed for safe use.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Potassium channel openers could help treat cardiovascular diseases and asthma but require better targeting to specific tissues for effective use.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

New treatments for low male hormones improved sexual function and mood but had unclear risks, especially for older men.

The guide explains how to study human skin fat cells and their tissue, aiming to improve research and medical treatments.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

Using polymeric micelles to deliver spironolactone topically could improve wound healing in skin affected by glucocorticoids.

Nourkrin® with Marilex® may increase hair count by 35.7% in postpartum hair loss.

MSC-Exos can aid organ development and offer therapeutic benefits for various conditions.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

UV photography can help identify people at higher risk for skin cancer, and male pattern baldness at age 45 is linked to a higher risk of certain skin cancers.

5α-reductase inhibitors can cause serious and possibly lasting sexual and psychological side effects.

Keratinocytes and adipose-derived stem cells can effectively heal difficult skin wounds.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

The skin is a complex barrier for drug penetration, but understanding its structure and interactions can improve drug delivery methods.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Thyroid hormones are important for skin health and might help treat skin diseases, but more research is needed to understand their effects fully.

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.

Certain RNA molecules are important for the development of wool follicles in sheep.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Genetic manipulations that extend lifespan in mice may not work as effectively in humans.