Search

everythinglearnresearchcommunity

for

Search:↓

Hair color production is closely linked to the active growth phase of hair in mice and may also influence hair growth itself.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

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

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

We need better ways to test and understand SARMs to make safer and more effective treatments.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

A certain genetic variant in the androgen receptor may predict the severity of COVID-19 in men.

Sex steroids affect the MafB gene differently in male and female hamsters.

Using neurohormones to control keratin can lead to new skin disease treatments.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.