Search

everythinglearnresearchcommunity

for

Search:↓

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

The review concludes that innovations in regenerative medicine, tissue engineering, and developmental biology are essential for effective tissue repair and organ transplants.

Zebrafish are useful for studying and developing treatments for human skin diseases.

Understanding skin structure and development helps diagnose and treat skin disorders.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

A woman's rare benign tumor that released both cortisol and testosterone was successfully removed, improving her health.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Men with early balding showed higher levels of certain genes linked to hair loss and possibly prostate cancer.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Forensic hair analysis for drugs is now more reliable and accurate.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Genetic marker rs12558842 strongly linked to male hair loss.

Minoxidil can reduce functions related to androgen receptors.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

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

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Targeting specific genes in certain pathways may help treat male pattern baldness.