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Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Vitamin D and calcium are essential for normal hair growth.

Heat treatment increases hair loss in certain mice.

Altering maternal cortisol during pregnancy can improve wool growth in Merino sheep.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Inducing survivin in normal tissues can protect against radiation damage.

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

OsPRX83 helps rice survive stress by improving stress response and antioxidant activity.

Alopecia Areata is linked to specific gut bacteria and metabolites, indicating a complex gut microbiome.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Rosehip Seed Oil may help hair grow by activating important growth pathways and increasing hair follicle size in mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Choosing the right starting dose of Clomiphene Citrate for ovulation induction in PCOS women is challenging; higher BMI and hormone levels may indicate resistance to the standard dose.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

Hirsutism is more linked to high androgen levels than acne or hair loss, and a mix of hormonal tests is best for diagnosis; certain treatments can reduce symptoms.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Human stem cells were turned into cells similar to those that help grow hair and showed potential for hair follicle formation.

PCOS may have evolved as an advantage in past environments with food scarcity.

The EDAR gene greatly affects hair thickness in Asian populations.