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

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

PIKFyve is essential for normal platelet function and its deficiency causes organ issues and macrophage infiltration.

PTHrP and its receptor can control blood vessel growth and hair development in mouse skin.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

DNMT3A is crucial for healthy skin and hair growth.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

IGF2BP3 gene is up-regulated in keloid patients, suggesting potential targets for treatment.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

HSPC016 gene is important for hair growth.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

Pannexin 3 is important for bone formation and the development of bone cells.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

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.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

MEX3A is crucial for maintaining intestinal stem cells in mice.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

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