Search

everythinglearnresearchcommunity

for

Search:↓

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

The document concludes that careful evaluation is key to diagnose and treat women with hair loss, with tests for thyroid, iron, and hormones as needed.

The most common skin problems in Indian children are infections and eczemas.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

The document explains how to identify different hair problems using a microscope.

Acquired Progressive Kinking of Hair is likely an early sign of male pattern baldness.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Women with androgen excess, especially those with PCOS, have a much higher risk of heart disease and stroke.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Alopecia areata involves immune response and gene changes affecting hair loss.

PRP shows promise for improving facial wrinkles, skin elasticity, and hair growth, but more research is needed to standardize its use and understand its effects.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Ultraviolet rays damage hair, smoking may cause hair loss, and good nutrition is important for hair health, but genetics mainly decide hair thickness.

Researchers found a new mutation causing total hair loss from birth.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

People with alopecia areata have higher insulin resistance.