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Subcutaneous trastuzumab improves some symptoms and doesn't harm overall quality of life in breast cancer patients.

Vitamin D levels in hair don't match those in blood, so hair isn't a reliable indicator of Vitamin D status.

Modern hair styling products don't repair hair but improve its surface and stability.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

3D imaging of skin biopsies offers better accuracy but is time-consuming and can't clear melanin.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Three specific 4-azasteroid-2-oximes showed strong enzyme inhibition, but less than finasteride.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A specific gene mutation causes long hair in Angora rabbits.

A specific gene mutation causes woolly hair and hair loss.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

EGCG may help treat alopecia areata by blocking certain immune responses and reducing specific harmful immune cells.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A mutation in the KRT25 gene causes a rare hair disorder with thin, woolly hair.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

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

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

An HIV patient's complete hair loss was reversed after switching from lopinavir/ritonavir to nelfinavir.

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

There are various effective hormone treatments for puberty induction in boys and girls with hypogonadism, and starting treatment early is important.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

Acid can block TRPV3 from outside the cell but boost its function from inside.

Oral lichen planus is a chronic disease causing mouth discomfort and sometimes needs immunosuppressive treatment.

Specific gene variants affect wool traits in Chinese Tan sheep.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Artificial skin grafts face immune rejection, but stem cells may improve future designs.