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Neuronatin is found in specific cells within rat testis, hair follicles, tongue, and pancreas, suggesting it has various roles in tissue development and function.

Understanding fetal skin development helps diagnose congenital skin diseases.

Certain miRNAs may play a role in sheep hair follicle development, which could help improve wool production.

Digit ratio likely doesn't predict male hair loss.

Low vitamin D levels may affect ovulation and progesterone in infertile women.

Certain microRNAs are important for sheep hair follicle development and could help improve wool quality.

Neonatal hair can help determine drug exposure during pregnancy.

Blood tests confirmed a baby in the womb had a CMV infection.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Higher anxiety during pregnancy is linked to lower cortisol levels in newborns' hair.

Higher prenatal anxiety is linked to lower cortisol levels in newborns' hair.

3D cultivation and prenatal stem cell exosomes improve stem cell treatment results, especially for hair loss and age-related issues.

Topical corticosteroids are the best initial treatment for children with Alopecia Areata.

Human prenatal skin develops an immune network early on that helps with skin formation and healing without scarring.

PFAS exposure in adolescence may delay puberty in females.

Immune cells are essential for early hair and skin development and healing.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Exposure to certain glycol ethers during pregnancy may be linked to lower verbal comprehension in children.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The FDA warned about safety issues with remdesivir and tofacitinib, finasteride is linked to suicidality, potent topical corticosteroids increase osteoporosis risk, henna can cause hemolysis in G6PD deficiency, chemotherapeutic agents can cause adverse reactions, drug interactions are common in cancer patients, ketamine can reduce at-risk drinking, high dose of anticholinergics increases dementia risk in Parkinson's patients, and prenatal exposure to second-generation antipsychotics increases pregnancy complications.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

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

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Neurotrophins, especially NGF, are crucial for pain development and management.

Higher early lead exposure is linked to delayed puberty in girls.