Search

everythinglearnresearchcommunity

for

Search:↓

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

New lipid/fiber microplexes improve mRNA therapy for degenerative diseases by enhancing cell function and treatment effectiveness.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

Microfluidic technology improves cell spheroid creation for better drug testing and tissue engineering.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Low-penetration genes might help personalize colorectal cancer prevention.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Mouse models help target specific genes in lymphatic cells for research.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

A new non-invasive laser system improves chronic disease management and metabolic health.

Repaglinide-loaded liponiosomal hybrids improve blood sugar control and insulin release better than regular Repaglinide.

The 2012 SLICC criteria provide an updated method for classifying Systemic Lupus Erythematosus.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

The technique effectively shows how human skin and hair cells form into ball-like structures.

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

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

Laminin 332 is essential for normal skin cell behavior and structure.

Lactate production is important for activating hair growth stem cells.

The tool iCOUNT helps understand how stem cells divide and affect tissue development and repair.

A mutation in the Sgkl gene causes defective hair growth in mice.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.