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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Finasteride may affect PNMT, causing side effects.

Tattooing guidelines focus on safety, hygiene, and following rules.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

Blocking BACE1 and BACE2 enzymes causes hair color loss in mice.

A 14-year-old girl with severe hair loss regrew her hair using upadacitinib.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Tyrosine kinase inhibitors show promise in treating some skin diseases but their definitive role in dermatology is still unclear.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Both dermatologists and patients in Japan agree that treatment success for alopecia areata is having 20% or less scalp hair loss.

The book is highly praised as an essential resource for plastic surgeons, despite minor gaps.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Mitochondrial problems in tooth cells lead to bad enamel and dentin development in mice.

Corin helps control salt and sweat release in sweat glands.

THA is a rare condition with no significant clinical consequences if thyroid function is normal.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

The document concludes that primary scarring alopecias cause permanent hair loss, have unpredictable outcomes, and lack definitive treatments, requiring personalized care.

Tumor suppressors help control inflammation in cancer and restoring their function could lead to new treatments.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

Existing drug dexamethasone may lower death risk in severe COVID-19 cases; more research needed for other drugs.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

Accurate diagnosis and effective oral treatment are key to managing tinea capitis and preventing its spread.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.