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

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

Paternal drug exposure can harm fertility, pregnancy outcomes, and offspring health, with specific drugs linked to various reproductive issues.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

FGF13 gene changes cause excessive hair growth in a rare condition.

Testosterone replacement is recommended for men with low testosterone levels and symptoms of hypogonadism.

Activating Notch signaling can kill basal cell carcinoma cells.

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

Shorter telomeres in white blood cells may increase the risk of a common type of hair loss.

A girl with lupus and trisomy X has a higher risk of bone problems like avascular necrosis and osteoporosis.

Certain gene variations in the Vitamin D Receptor are linked to higher risk of female hair loss.

Epigenetic factors play a crucial role in skin health and disease.

High DHEA and short cervical length in women with PCOS and recurrent miscarriages may harm pregnancy outcomes.

Finasteride and Dutasteride can improve hair growth in male baldness but may cause temporary sexual dysfunction and possibly affect fertility.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

The Hedgehog Signaling Pathway is important for skin and hair development and skin cancer treatment, but more research is needed to understand it fully.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Human skin cells have a high-affinity system for biotin transport, crucial for skin health.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Potassium channel openers help form elastic fibers in arteries and can treat elastin deficiency and hypertension.

The review suggests new ways to classify ejaculation problems and recommends different treatments based on the type of issue.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

New information suggests that metformin might help more women with PCOS and infertility, not just those with glucose issues.

A rare skin condition causes red and dark patches on the face and limbs.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.