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TCDD reduces EGF receptor activity and causes various developmental changes in animals.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Krtap11-1 is important for hair strength and structure.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Fatty acid transport protein 4 is essential for skin and hair development.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Human hair follicles have a unique way of using energy and might use the Cori cycle; blocking CCR5 could help treat hair loss.

Acitretin effectively prevented skin cancer in a patient with late-onset Rothmund-Thomson syndrome.

CRISPR/Cas systems show promise for cancer treatment by targeting miRNAs, but delivery and specificity challenges remain.

A truncated protein linked to breast cancer may change cell adhesion.

TRPA1 and TRPV1 channels don't affect mechanotransduction in rat sinus hair follicles.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.