Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

ErbB2 signaling is crucial for skin cell growth and cancer development in mice.

Twist2 is essential for scarless skin healing and hair growth in mouse fetuses.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

KAP8.2 gene variations affect cashmere quality in goats.

Mutations in the KRT16 gene can cause skin and nail disorders.

VEGFR-2 is active in hair follicles, sebaceous glands, sweat glands, and skin on the human scalp.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

A substance called 15-deoxy prostaglandin J2 can cause hair follicle cells to die, which might explain how prostaglandin D2 can lead to hair loss.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Defective protein folding due to a mutation is key in ANE syndrome.

Two new gene mutations cause a rare hair disorder.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.