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

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

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Hydrogel scaffolds can help wounds heal better and grow hair.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

A patient lost all their hair while on rheumatoid arthritis medication.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

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

A specific gene mutation causes long hair in Angora rabbits.

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

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

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

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

Re-evaluating minoxidil, reducing sodium intake, and addressing arteriolar hypertrophy can improve hypertension management.

The new adhesive nanoparticles are effective for delivering Minoxidil to the scalp without skin irritation.

Older obese women with PCOS have higher cardiovascular and metabolic risks despite lower androgen levels.

The guideline recommends mental health involvement in diagnosing gender identity disorder and outlines hormone and surgical treatment protocols, emphasizing safety, informed consent, and long-term monitoring.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

Nanostructured lipid carriers are effective for treating hyperpigmentation in women aged 30-40.

Selective non-steroidal inhibitors of 5α-reductase type 1 can help treat DHT-related disorders.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

New compounds were made that effectively block enzymes related to prostate issues and hair loss.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

The enzyme steroid sulfatase is linked to breast cancer and other conditions, and inhibitors are being developed for treatment.

Anabolic steroids can build muscle and strength but have risks and need more research on their clinical benefits and side effects.

The guidelines suggest lifestyle changes, diet adjustments, and personalized medication to manage dyslipidemia and reduce heart disease risk.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.