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A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Blocking CRF1 receptors improved male hormone levels and reduced testicular tumor size in men with a specific adrenal condition.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Reduced TRPS1 leads to increased STAT3 and SOX9 in hair follicles, affecting hair growth.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

Certain immune cells in atopic dermatitis skin could be targeted for treatment.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Vitamin D3 and its receptor help protect skin from UVB-related cancer.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

TRPV3 and TRPV6 channels change structure to regulate calcium and heat responses.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

CCC1 is essential for ion balance and proper plant cell function.

The CRABP I gene in cashmere goats is highly conserved but has unique features at specific amino sites.

Tissue-resident memory T cells can protect against infections and cancer but may also contribute to autoimmune diseases.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.