Search

everythinglearnresearchcommunity

for

Search:↓

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

The ZIP13 variant is linked to abnormal hair quality.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Specific gene variants affect wool traits in Chinese Tan sheep.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

CT60 polymorphism might increase the risk of Alopecia Areata.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Genetic differences affect COVID-19 severity and treatment development.

The KRTAP19-5 gene affects wool curvature in Chinese Tan sheep, with Variant B reducing curvature.

KRT71 gene variants may influence camel hair shape but don't fully explain it.

Woodhouse-Sakati syndrome shows varied symptoms and genetic differences within families.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

Certain genetic markers can indicate a person's risk of developing prostate cancer.

No significant link was found between the studied genes and female hair loss in the Polish population.

Researchers found a genetic region that influences the number of coat layers in dogs.

Certain VDR gene changes can affect melanoma risk.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

A specific gene mutation causes sparse, brittle hair in a family.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

CS12192 effectively treats alopecia areata with better safety than current options.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.