Search

everythinglearnresearchcommunity

for

Search:↓

Dandruff might be caused by changes in how hair follicles naturally release oils and an immune response to this imbalance.

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

CD98hc's role in skin health decreases with age.

Skin aging is due to impaired stem cell mobilization or fewer responsive stem cells.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

Platelet-rich treatments can help improve wound healing and tissue repair.

Formestane is a preferred second-line treatment for advanced breast cancer in postmenopausal women because it's effective and has fewer side effects.

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

The conclusion is that proper diagnosis and long-term treatment, including medication, hair removal, and lifestyle changes, are important for improving hirsutism, especially in PCOS patients.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

The conclusion is that the type of writing system used can significantly affect the translation of a text.

Hair follicles in mutant mice self-organize into ordered patterns within a week.

Understanding skin structure and development helps diagnose and treat skin disorders.

Latanoprost-loaded nanotransfersomes could help treat hair loss by promoting hair growth.

Microneedling with 5% minoxidil improves hair loss in Chinese men by activating Wnt/ß-catenin pathway.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Biomimetic scaffolds are better than traditional methods for growing cells and could help regenerate various tissues.

The document concludes that the skin is a complex organ providing protection, sensation, and healing, with challenges in treating conditions like itchiness.

A balanced diet with proteins, vitamins, and minerals is crucial for managing skin disorders.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

The document concludes that Telogen Effluvium is a hair loss disorder that can be assessed with the modified wash test and may be treated with clobetasol foam, with patient management being important.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.