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The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

GRK2 is essential for healthy hair follicle function, and its absence can lead to hair loss and cysts.

A specific enzyme is essential for proper hair follicle stem cell development and healthy skin.

Low ferritin levels are linked to increased hair loss; no link found between vitamin B12, TSH levels, and hair loss.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

People with alopecia have a higher risk of thyroid cancer.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Neonate scalp hair is thinner, lacks a medulla, and has smaller follicles compared to adult hair.

Hair damage shows as fragility, dullness, and discoloration, varies by ethnicity, and is worsened by cosmetic procedures and diseases.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Hair follicles can be used to quickly assess drug effects in cancer treatment.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

A gene mutation in Lama3 is linked to a common type of hair loss.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

White piedra is often a co-infection with a specific bacterial infection.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Fusidic acid successfully treated a rare scalp infection with hair regrowth and no recurrence after 6 months.

The document describes the signs of different common types of hair loss.

Leydig cell tumors can cause high testosterone and symptoms in postmenopausal women, and removing them improves symptoms.

Early detection and treatment of hair-thread tourniquet syndrome in young girls is important to prevent serious harm.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

Perming significantly changes hair's molecular structure, while shampoo and conditioner do not.

A specific gene mutation causes Olmsted syndrome.

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.