Search

everythinglearnresearchcommunity

for

Search:↓

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Akebia quinata and Akebia trifoliata have many health benefits and potential medical uses.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Non-coding RNAs are crucial for skin development and health.

A mouse gene mutation increases the risk of skin cancer.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Jasmonic acid helps plants grow, defend against threats, and survive stressful conditions like drought and salt.

There are various effective hormone treatments for puberty induction in boys and girls with hypogonadism, and starting treatment early is important.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Skin and nail problems like hair loss, dry skin, and fungal infections are common in people with long-term Type 2 Diabetes and can be prevented with good blood sugar control and foot care.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Maritime pine bark has various chemical components useful for different industrial uses.

Patients with long COVID after Omicron had fewer hospitalizations and milder symptoms but more fatigue, insomnia, and cough compared to those with Delta.

Inherited color dilution in rabbits is linked to DNA methylation changes.

Certain growth factors significantly affect hair loss in women with telogen effluvium.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The KRTAP21-2 gene affects wool length and quality in sheep.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

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.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

Male and female human hairs have different microscopic structures that can help in forensic analysis.

Cirrhosis affects quality of life with various symptoms, requiring a holistic, multidisciplinary approach for management.

Tamsulosin increases the risk of floppy iris during eye surgery.

Finasteride harms Daphnia magna's reproduction, growth, and metabolism.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.