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The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

No link found between specific genes and female pattern hair loss.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Finasteride effectively treats enlarged prostate and male baldness, improves symptoms of hirsutism in women, but doesn't work for acne, and may delay prostate cancer progression with few side effects.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Isoallopregnanolone may be a safe and effective treatment for reducing tics in a mouse model of Tourette syndrome.

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

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

FGF-1 causes spiral ganglion neurites to branch more.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Researchers found a gene mutation responsible for a rare hair loss condition.

The study concluded that androstendione and DHEA are important for diagnosing high male hormone levels in women with excessive hair growth.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

High levels of the protein Flightless I worsen ulcerative colitis symptoms in mice.