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The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Chitosan slows root hair growth and causes a buildup of callose at low concentrations, but at high concentrations, it only inhibits growth without callose buildup.

RoPod helps study plant root cell changes and autophagy with minimal stress.

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

The Ysc84/SH3yl1 protein family is important for cell movement and the process of taking in materials by interacting with actin and cell membranes.

Near-infrared probes can safely and effectively image cysteine protease activity for disease diagnosis.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

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

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

S100A3 protein is crucial for hair shaft formation in mice.

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A new DSG4 gene mutation causes hair defects in a young girl.

A new mouse mutation causes skin and hair defects due to a gene change.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

S100A6 is important for cell functions and can help diagnose and treat diseases.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

The cyst had unusual keratin spherules and resembled bone marrow.

Researchers found a non-functional sheep keratin gene due to mutations.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

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

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.