Search

everythinglearnresearchcommunity

for

Search:↓

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

The document concludes that early and accurate diagnosis of hair loss on the top of the scalp in Black men is important to distinguish CCCA from other types of hair loss.

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

The cause of Frontal fibrosing alopecia, a type of hair loss, is complex, likely involving immune responses and genetics, but is not fully understood.

Some women with PCOS have rare genetic variants linked to the condition.

Disrupted stem cell signals in hairpoor mice cause hair loss.

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

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

The study found that specific proteins are markers of hair follicle development in human fetuses.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

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.

Certain skin proteins can form anchoring structures without the protein AMACO.

Blocking a certain signal in the gp130 receptor can improve tissue healing and lessen osteoarthritis symptoms.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The research found specific genes and pathways that control fur development and color in young American minks.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

New methods to test hair growth treatments have been developed.

Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Long scalp hair evolved for cooling and social signaling.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.