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research A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus

November 2012 in “Experimental and Clinical Endocrinology & Diabetes”

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

research Proposal Statement

January 2025 in “KeiO Associated Repository of Academic Resources (Keio University)”

research Reversible severe myopathy during treatment with finasteride

15 citations , April 1997 in “Muscle & Nerve”

research Reversible severe myopathy during treatment with finasteride

5 citations , April 1997 in “Muscle & Nerve”

Efficacy and Safety of a Botanical Shampoo Containing Morus Alba Root Extract in Republic of Korea: A Single-Center, Open-Label, Pilot Study in Mild to Moderate Non-Scarring Alopecia of the Scalp

research Efficacy and safety of a botanical shampoo containing Morus alba root extract in Republic of Korea: a single-center, open-label, pilot study in mild to moderate non-scarring alopecia of the scalp

September 2023 in “Medical lasers”

The botanical shampoo with Morus alba root extract is safe and effective for treating hair loss.

Unexpectedly High Carrier Rates and Genotype/Phenotype Correlation: LIPH Mutations in Japanese Autosomal Recessive Woolly Hair/Hypotrichosis

research Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis

September 2016 in “Journal of Dermatological Science”

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

research The role of CYP19A1 and ESR2 gene polymorphisms in female androgenetic alopecia in the Polish population

October 2021 in “Postepy Dermatologii I Alergologii”

No significant link was found between the studied genes and female hair loss in the Polish population.

research Spectrophotometric and Stability Indicating RP-HPLC-PDA method for Simultaneous Determination of Finasteride and Tamsulosin in Combined Tablet Dosage form

1 citations , December 2009 in “Asian Journal of Research in Chemistry”

The methods accurately measure Finasteride and Tamsulosin in tablets.

research Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene

36 citations , January 2010 in “Journal of Pediatric Endocrinology and Metabolism”

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

research ABHRS Results Announced

January 1998 in “International Society of Hair Restoration Surgery”

27 out of 32 candidates passed the hair restoration surgery exam.

research Flurandrenolide

January 2004

research Delayed diagnosis of Kearns-Sayre syndrome in a 38-year-old male patient: a case report.

2 citations , January 2008 in “International Journal of Neuroscience”

A 38-year-old man was diagnosed late with Kearns-Sayre syndrome after being wrongly treated for epilepsy.

research 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing

July 2024 in “Journal of Investigative Dermatology”

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

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.

A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long-Term Side Effects After Finasteride Discontinuation

research A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation

16 citations , September 2014 in “International Journal of Biological Markers”

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

research A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing

January 2021 in “Research Square (Research Square)”

Chinese fine-wool sheep have genetic variations linked to traits like milk and health, with some genes under strong selection.

research A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome

152 citations , April 2002 in “The journal of investigative dermatology/Journal of investigative dermatology”

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

research Liposomal Bupivacaine

August 2018 in “Dermatologic Surgery”

research Efficacy and Safety of Ritlecitinib in the Asian Subpopulation of the ALLEGRO ‐2b/3 and ALLEGRO ‐ LT Clinical Studies for Alopecia Areata

February 2026 in “The Journal of Dermatology”

Ritlecitinib effectively regrows scalp, eyebrow, and eyelash hair in Asians with alopecia areata and is safe.

research 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study

April 2018 in “Journal of Investigative Dermatology”

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

Copy Number Variation Regions in Nellore Cattle: Evidence of Environmental Adaptation

research Copy number variation regions in Nellore cattle: Evidences of environment adaptation

21 citations , November 2017 in “Livestock science”

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

research Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients

November 2025 in “Clinical Cosmetic and Investigational Dermatology”

LIPH mutations cause woolly hair in some Chinese people.

A Synbiotic Preparation (SIM01) for Post-Acute Covid-19 Syndrome in Hong Kong (Recovery): A Randomised, Double-Blind, Placebo-Controlled Trial

research A synbiotic preparation (SIM01) for post-acute COVID-19 syndrome in Hong Kong (RECOVERY): a randomised, double-blind, placebo-controlled trial

6 citations , December 2023 in “Lancet. Infectious diseases/The Lancet. Infectious diseases”

SIM01 significantly reduced post-COVID symptoms and is safe.

Search

for
Search:

Research

research A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus

research Proposal Statement

research Reversible severe myopathy during treatment with finasteride

research Reversible severe myopathy during treatment with finasteride

research Efficacy and safety of a botanical shampoo containing Morus alba root extract in Republic of Korea: a single-center, open-label, pilot study in mild to moderate non-scarring alopecia of the scalp

research Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis

research The role of CYP19A1 and ESR2 gene polymorphisms in female androgenetic alopecia in the Polish population

research Spectrophotometric and Stability Indicating RP-HPLC-PDA method for Simultaneous Determination of Finasteride and Tamsulosin in Combined Tablet Dosage form

research Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene

research ABHRS Results Announced

research Flurandrenolide

research Delayed diagnosis of Kearns-Sayre syndrome in a 38-year-old male patient: a case report.

research 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing

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

research A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation

research A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing

research A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome

research Liposomal Bupivacaine

research Efficacy and Safety of Ritlecitinib in the Asian Subpopulation of the ALLEGRO ‐2b/3 and ALLEGRO ‐ LT Clinical Studies for Alopecia Areata

research 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study

research Copy number variation regions in Nellore cattle: Evidences of environment adaptation

research Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients

research A synbiotic preparation (SIM01) for post-acute COVID-19 syndrome in Hong Kong (RECOVERY): a randomised, double-blind, placebo-controlled trial

research The Efficacy of HDDPiW-jSB Solution on Docetaxel-Induced Alopecia of Rats

research Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

research Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China

research Natural Transplants, Hair Transplantation Clinic. Hair Transplantation near Ocean Ridge Call (844) 327-4249.

research Identification and Detection of Finasteride Polymorphs in Finasteride Tablets by FT-Raman Spectroscopy

research Notes from the Editor Emeritus, 1999–2001: The Buyer’s Remorse Dilemma

research 085 Post-translational regulation of hair keratins in transfected COS-1 cells