June 2026 in “Drug Delivery and Translational Research” The study presents a solid microneedle booster (SMB) as an advanced microneedling platform for treating androgenetic alopecia (AGA). The SMB integrates spring-driven perpendicular stamping with simultaneous liquid dosing, improving microchannel reproducibility and early transport. Tests on porcine skin revealed that SMB achieved greater microchannel surface coverage and deeper penetration than a roller. It also enhanced early-phase permeation, accelerating hair regrowth when combined with minoxidil (MXD) in vivo. Histological analysis showed increased follicle enrichment in the SMB + MXD group. SMB provides a one-step, directionality-controlled microneedling method that enhances early transport and promotes follicular maturation, with potential for broader dermatologic applications.
1 citations
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November 2024 in “Diabetes Metabolic Syndrome and Obesity” A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.
51 citations
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December 2006 in “Mammalian Genome” August 2018 in “Journal of the American Academy of Dermatology” 
November 2022 in “Nihon Nyuusankin Gakkaishi/Nihon Nyūsankin Gakkaishi” The lotion with N793 strain significantly increased hair density and reduced hair loss safely.
March 2026 in “International Journal of Pharmaceutics and Drug Analysis” A reliable, cost-effective method was developed for accurately measuring finasteride in medicines.
1 citations
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November 2004 in “Hair transplant forum international” The document couldn't be read, so there's no conclusion to summarize.
July 1998 in “Hair transplant forum international” The document's content could not be processed or understood.
10 citations
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January 1996 The document's conclusion cannot be determined as the content is not accessible or understandable.
The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.
March 2011 in “Hair transplant forum international” Unable to provide a summary as no conclusion is provided in the text.
November 2009 in “한국분석과학회 학술대회” 2 citations
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December 2007 in “CRC Press eBooks” October 2005 in “CRC Press eBooks” 6 citations
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August 2024 in “BMC Ophthalmology” New genetic variants linked to albinism were found in Pakistani families.
May 2025 in “Reactions Weekly” 
January 2016 in “Hair transplant forum international” The document's content cannot be summarized because it is not accessible or understandable.
June 2018 in “Reactions Weekly” A 65-year-old man developed a serious skin cancer linked to a drug he was taking for a fungal infection after a bone marrow transplant.
136 citations
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January 2013 in “International Journal of Trichology” 14 citations
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March 2018 in “The American journal of case reports” People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.
![Optimization of Anti-Hair Loss Cream Mixing Process with Saw Palmetto Extract [Serenoa Repens] Using Mixing Temperature and Rotation Speed Comparison: Application of Factorial Design](/images/research/b2677f7e-1e4f-45a9-b3cd-8657b1c20a30/small/23373.jpg)
The conclusion cannot be provided because the document content is not available.
May 1997 in “Hair transplant forum international” The document's conclusion cannot be determined because the content is not available.
August 2016 in “Journal of Investigative Dermatology” 6 citations
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October 2001 in “British Journal of Ophthalmology” 6 citations
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January 2004 in “Acta dermato-venereologica” 
4 citations
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January 2017 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism” Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.
2 citations
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July 2012 in “BMJ” FFA can be mistaken for rosacea, requiring specific treatment for accurate diagnosis and management.
The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.
1 citations
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September 2023 in “Frontiers in Genetics” A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.
September 2019 in “Journal of Investigative Dermatology” Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.