Search

everythinglearnresearchcommunity

for

Search:↓

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Gene mutations can cause problems in male genital development.

Some drugs can cause rare but potentially deadly skin reactions, and early treatment and avoiding the drug again are key.

Psoriasis is linked to other autoimmune diseases and involves a specific inflammatory process.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Early diagnosis and treatment are crucial for preventing permanent hair loss in various scalp conditions, and while new treatments are promising, more research is needed to evaluate their effectiveness.

A male with aromatase deficiency improved bone health with estradiol treatment.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Activin activation in skin cells speeds up wound healing without affecting scar quality.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Six new hair loss factors in men not linked to female hair loss.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

Low androgen levels can still cause female pattern hair loss.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.