Search

everythinglearnresearchcommunity

for

Search:↓

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

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.

The conclusion is that androgenetic alopecia and senescent alopecia have unique gene changes, suggesting different causes and potential treatments for these hair loss types.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

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

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Mutations in the KRT85 gene cause hair and nail problems.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Only a few hair-specific keratins are linked to inherited hair disorders.

Certain gene variations may increase the risk of hair loss in Egyptians.

FGF13 gene changes cause excessive hair growth in a rare condition.

Hair protein composition is similar across different races and shapes.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.