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Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

Sheep cells were successfully modified to include a spider silk protein gene.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Seven new genetic risk areas for prostate cancer were found.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

Certain genes may influence hair loss differently in men and women.

FGF13 gene changes cause excessive hair growth in a rare condition.

Capivasertib improves survival in certain breast cancer cases but requires careful management of side effects.

Pemigatinib may be effective for treating ZMYM2::FGFR1 fusion-positive leukemia.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

PGD2 stops hair growth and is higher in bald men with AGA.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

AP-1 controls tumor cell type by affecting key signaling pathways.

Mitochondrial features can predict colorectal cancer outcomes and improve immunotherapy.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

SQSTM1 is linked to increased risk of alopecia areata.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

β1 integrin is essential for the survival, growth, and movement of human epithelial progenitor cells.