Search

for
Search:

Sort by

Research

120-150 / 1000+ results

research LB793 A phase 1, open-Label, single ascending dose study in healthy subjects of the safety, tolerability and pharmacokinetics of ASLAN004, a novel IgG anti-IL-13 receptor alpha 1 Inhibitor

1 citations , August 2021 in “Journal of Investigative Dermatology”

ASLAN004 was safe and well-tolerated, supporting further development for treating certain diseases.

research Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

40 citations , December 2010 in “Human Genetics”

research The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals

9 citations , March 2009 in “Psychoneuroendocrinology”

Certain gene variations are linked to better memory in healthy Chinese women.

research CD8-positive Lymphocytes in Graft-Versus-Host Disease of Humanized NOD.Cg-Prkdcscid Il2rgtm1Wjl/SzJ Mice

7 citations , February 2015 in “Journal of comparative pathology”

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

Glutathione Distribution by Quantitative MALDI Imaging in Reconstructed Human Skin Upon Activation of GSH Biosynthesis by Nrf2 Pathway Activator

research 1331 Glutathione (GSH) distribution by quantitative MALDI imaging in reconstructed human skin upon activation of GSH biosynthesis by Nrf2 pathway activator

April 2018 in “Journal of Investigative Dermatology”

Resveratrol activates the Nrf2 pathway in human skin, significantly increasing the production and distribution of the antioxidant glutathione.

research Successful Treatment of Scalp Micropigmentation With 1064 nm Picosecond Nd:YAG Laser

December 2020 in “Lasers in Surgery and Medicine”

Laser safely and effectively removes unwanted scalp micropigmentation.

Case of Autosomal Recessive Woolly Hair/Hypotrichosis with Compound Heterozygous Mutations in the LIPH Gene at c.742C > A and c.614A > G: The First Japanese Case

research Case of autosomal recessive woolly hair/hypotrichosis with compound heterozygous mutations in the LIPH gene at c.742C > A and c.614A > G: The first Japanese case

February 2023 in “Journal of dermatology”

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

research L-Ornithine ketoacid-transaminase assay in hair roots of homozygotes and heterozygotes for gyrate atrophy

8 citations , June 1981 in “Clinica Chimica Acta”

research 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair

August 2016 in “Journal of Investigative Dermatology”

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

research Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot

April 2026 in “Human Genome Variation”

This study reports on a Pakistani family with three individuals affected by IFAP syndrome type I, linked to the recurrent MBTPS2 splice-site variant c.970+5G>A. This variant has also been identified in Chinese and Argentinian families. Haplotype analyses indicate that this is a recurrent mutational hotspot rather than a result of a founder effect. The study also notes variability in phenotypic severity among the families, suggesting the presence of additional modifying factors.

Antioxidant and Hair Growth Effects of Red Ginseng Extract (GS-E3D)

research 홍삼가수분해추출물(GS-E3D)의 항산화 및 양모 효과

January 2017 in “생약학회지”

Red ginseng extract (GS-E3D) may promote hair growth and has antioxidant and anti-inflammatory properties.

research 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome

April 2017 in “Journal of Investigative Dermatology”

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

research Photoprotective and immunoregulatory capacity of ginsenoside Rg1 in chronic ultraviolet B-irradiated BALB/c mouse skin

6 citations , July 2013 in “Experimental and Therapeutic Medicine”

Ginsenoside Rg1 protects mouse skin from UVB damage and helps control inflammation.

research Ginsenoside Rb1 promotes the growth of mink hair follicle via PI3K/AKT/GSK-3β signaling pathway

28 citations , May 2019 in “Life Sciences”

Ginsenoside Rb1 from Panax ginseng helps mink hair grow by activating certain cell signals.

research Inducible expression of gasdermin A3 in the epidermis causes epidermal hyperplasia and skin inflammation

12 citations , July 2015 in “Experimental Dermatology”

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

research Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep

19 citations , January 2023 in “Genes”

Certain genes influence wool, growth, and reproduction traits in Uruguayan Merino sheep.

research Analysis Polymorphism of Androgen Receptor in Cases of Androgenetic Alopecia

January 2011 in “The Chinese Journal of Dermatovenereology”

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

research BC05 Technological and clinical demonstration of a skin ageing analysis prototype

June 2023 in “British Journal of Dermatology”

The prototype for analyzing skin aging works technically and clinically.

research 022 Randomized, double-blind, placebo-controlled, single-centre, phase I safety study of intradermal injections of autologous fibroblasts isolated from the non-bulbar dermal sheath of the hair follicle to treat skin aging

September 2017 in “Journal of Investigative Dermatology”

RCS-01 is safe and may help rejuvenate aging skin.

research 576 INTASYL PH-762: Intratumoral immunotherapy targeting PD-1

July 2024 in “Journal of Investigative Dermatology”

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

research Long pulse 1,064‐nm neodymium‐doped yttrium aluminum garnet laser in aesthetic dermatology

9 citations , April 2019 in “Dermatologic Therapy”

The 1,064-nm Nd:YAG laser is versatile and effective for treating leg veins, hair removal, and skin rejuvenation, especially in darker skin types.

research Single‐center study to determine the safety and efficacy of CT‐707 in Chinese patients with advanced anaplastic lymphoma kinase‐rearranged non‐small‐cell lung cancer

5 citations , March 2020 in “Thoracic Cancer”

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

research UJI AKTIVITAS SEDIAAN CREAMBATH EKSTRAK DAUN WARU (Hibiscus tiliaceus L.) TERHADAP PERTUMBUHAN RAMBUT KELINCI NEW ZEALAND WHITE

January 2019

Waru leaf creambath can speed up hair growth in rabbits, especially at 37.5% concentration.

research ERRATUM

October 2002 in “Dermatologic Surgery”

research 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum

November 2025 in “Journal of Investigative Dermatology”

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

research Disposable Linear Slot Punches

September 1997 in “International Society of Hair Restoration Surgery”

research IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep

February 2026 in “Small Ruminant Research”

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

research Release systems based on self-assembling RADA16-I hydrogels with a signal sequence which improves wound healing processes

1 citations , April 2023 in “Scientific Reports”

Self-assembling RADA16-I hydrogels with bioactive peptides significantly improve wound healing.

research The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs

November 2025 in “BMC Genomics”

Wrinkled skin in Xiang pigs is linked to gene changes related to oxidative stress and the extracellular matrix.

research A homozygous nonsense mutation identified in COL7A1 in a family with autosomal recessive dystrophic epidermolysis bullosa

September 2024 in “Journal of Medicine and Life”

A specific gene mutation causes a severe skin disorder in a family.

← Previous page Next page →