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Cadd4 effectively reduces cholesterol levels without side effects.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Certain herbal compounds, especially from bitter melon, can inhibit cancer growth and promote hair growth by blocking PAK1.

Abnormal contraction of connective tissue in hair follicles causes hair loss by killing off important cells, and treating this could improve hair growth.

Tocilizumab therapy may cause skin and hair conditions like halo naevi, vitiligo, and alopecia areata.

A rare case of Cushing's syndrome and pheochromocytoma requires careful re-evaluation to avoid complications.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

Testing for the NUDT 15 variant is crucial before starting azathioprine, especially in Asians.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Proper diet management is crucial for preventing severe symptoms in phenylketonuria.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

Cepharanthine may help treat COVID-19 by targeting similar pathways as other inflammatory diseases.

Mutations in keratin genes cause cell fragility and various skin disorders.

A genetic variant in the KRT25 gene causes tightly curled hair.

Combining L-cysteine, NAC, and a MET inhibitor significantly kills cervical cancer cells.

Trilostane helped a cat with a hormone issue but the cat later died from a kidney infection.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Selenium imbalance can cause hair loss and skin issues.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The woman has scurvy and needs more vitamin C.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.