Search

everythinglearnresearchcommunity

for

Search:↓

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The study developed a 3D model that closely imitates remaining ovarian cancer after treatment and identified a potential drug targeting resistant cancer cells.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

Pueraria mirifica extract may help treat benign prostatic hyperplasia.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

MYB83 limits root hair growth and helps plants tolerate nutrient deficiencies.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

New method accurately measures finasteride and M3 in urine, helping evaluate pharmacokinetics.

Matriptase imbalance contributes to cancer development and spread.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Using an anti-ICAM-1 antibody with rapamycin improves hair transplant survival in monkeys.