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Low testosterone in men is a risk factor for a specific heart rhythm issue, and testosterone treatment may help prevent it.

Type 3 Innate Lymphoid Cells help maintain skin health and balance, and are involved in skin diseases and healing.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Genetic mutations can affect female sexual development, requiring personalized medical care.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

The 2018 guideline for PCOS suggests new diagnostic criteria and treatments, but recognizes the need for more research.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

EGFR helps control how hair grows and forms without needing p53 protein.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.