Search

everythinglearnresearchcommunity

for

Search:↓

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

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

BMPR1a-ECD reduces wrinkles much more effectively than retinoic acid.

Activating Kras in mouse skin causes excess skin and hair loss.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

Certain defective glucocorticoid receptor mutants move faster inside cell nuclei and work less effectively.

A KRT32 gene variant causes loose anagen hair syndrome.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

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

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

HPV8 causes skin cancer by expanding specific skin stem cells.

Iron deficiency in mothers causes hair loss in their baby mice.

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

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Mice with extra PKCδ resist chemical-induced skin cancer but not UV-induced.

Trichohyalin and peptidylarginine deiminase type III are found together in rat hair follicles, with trichohyalin being modified after expression.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

β-catenin, Shh, and Bmp signaling control hair follicle development.

Zebrafish help understand genetic causes of skin pigment disorders like albinism.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

Pygopus 2 helps ovarian cancer cells grow by aiding ribosomal RNA production, independent of Wnt signaling.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.