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Using platelet-rich plasma in hair restoration surgery significantly improves hair density after 6 months and is safe to use.

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

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

The conclusion is that it's important to tell apart alopecia areata from lipedematous alopecia for proper treatment, as alopecia areata can be reversed.

Both enzyme forms can sulfate minoxidil.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

A specific gene mutation causes congenital hair loss.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

The document's conclusion cannot be provided because the document is not available or cannot be read.

A dog's skin calcification condition resolved without treatment after a bacterial infection.

Anesthesia and surgery can cause temporary hair loss, but hair usually grows back without treatment.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Fermented soy protein may help prevent bone loss by affecting bone cell activity.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Removing part of the vitamin D receptor stops vitamin D from working properly.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

PD‐L1 and PD‐L2 may not effectively control immune activation in alopecia areata.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

L. plantarum MTCC 1325 may help improve memory and cognitive functions in Alzheimer's.

Higher HDAC1 levels in alopecia areata suggest HDAC inhibitors might help treat it and acne.

Efficient enzyme function relies on specific residue interactions and structural coordination.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.