Search

everythinglearnresearchcommunity

for

Search:↓

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

Low-penetration genes might help personalize colorectal cancer prevention.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

A specific mutation in PA-PLA1α causes abnormal hair growth.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

PAON shows skin patterns due to genetic mosaicism.

Two siblings have a rare hair condition caused by a new genetic variant.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Progesterone and its metabolites affect myelin protein expression differently in male and female rat Schwann cells.

Mutations in the TSPEAR gene cause a new form of ectodermal dysplasia affecting hair and tooth development.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Men with more CAG repeats in the androgen receptor gene and lower testosterone levels may experience more severe COVID-19.

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

The compound GD-23 may reduce anxiety like diazepam by targeting the TSPO receptor.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Certain genetic variations in the SHBG gene are linked to an increased or decreased risk of PCOS in Mediterranean women.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Mutations in the HOXC13 gene cause hair and nail development issues.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.