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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.

Dual TCR Treg cells are common in mouse tissues and vary by location.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

Colorectal cancer's ability to spread is due to changes in many genes, not just one.

A new gene mutation linked to a skin condition was found in a Spanish family.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

miR-144 affects hair growth by interacting with Lhx2.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Long non-coding RNA Xist plays a key role in sex bias in lupus and rheumatoid arthritis, especially in females.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Understanding snoRNA regulation may help slow skin aging.

Two specific genetic markers increase the risk of hair loss in Asian populations.

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

HLA-DRB5 and other genes may be linked to alopecia universalis.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

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