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Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets (HVDRR): Clinical Heterogeneity and Long-Term Efficacious Management of Eight Patients from Four Unrelated Arab Families with a Loss of Function VDR Mutation

research Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

6 citations , June 2018 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism”

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

research Newly formed Asian Association of Hair Restoration Surgeons (AAHRS)

July 2010 in “Hair transplant forum international”

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

research A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome

34 citations , September 2010 in “Clinical and Experimental Dermatology”

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

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 Finasteride/spironolactone

May 2024 in “Reactions weekly”

research 034 Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1

September 2019 in “The journal of investigative dermatology/Journal of investigative dermatology”

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

research Assessing tolerability and physiological responses to 17α-estradiol administration in male rhesus macaques

9 citations , March 2023 in “GeroScience”

research Novel D323G mutation of DSG4 gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix

8 citations , July 2015 in “International Journal of Dermatology”

A new DSG4 gene mutation causes hair defects in a young girl.

research Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3

56 citations , January 2014 in “Journal of Investigative Dermatology”

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

research Editor's notes

March 1998 in “Hair transplant forum international”

The document could not be processed or understood.

research A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb

5 citations , June 2008 in “British Journal of Dermatology”

research Phase I safety and pharmacokinetic study of SU-014813 in combination with docetaxel in patients with advanced solid tumours

22 citations , May 2011 in “European Journal of Cancer”

The drug combination was safe and showed promise in treating advanced tumors.

research Role of ASLNC168501 in regulating hair follicle stem cell activity via the AR/miR-128-3p/IGF-1 pathway

January 2026 in “Figshare”

ASLNC168501 may help treat hair loss by boosting hair follicle stem cell activity.

research Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling

February 2024 in “Plant Cell Reports”

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

research Frontal hairline design

November 2009 in “Cambridge University Press eBooks”

The document's conclusion cannot be provided because the content is not accessible.

research Med Check

May 2011 in “Psychiatric News”

Horizant has risks like other seizure drugs, Johnson & Johnson misled about Risperdal, and Quanterix found a possible link between brain oxygen loss and Alzheimer's markers.

research Natural Transplants, Hair Transplantation Clinic. Hair Transplant Growth Chart near Manalapan Call (844) 327-4249.

August 2023 in “Zenodo (CERN European Organization for Nuclear Research)”

research Editor's notes

4 citations , November 1996 in “Hair transplant forum international”

The document could not be processed for a summary.

research Clinical presentations of polycystic ovary syndrome in a tertiary care centre of southern Rajasthan, India

October 2019 in “Obsgyne Review Journal of Obstetric and Gynecology of Siddharth Health Research and Social Welfare Society”

The document's conclusion cannot be provided as the content is not available for summarization.

research Letter: Repair of severed brachial plexus.

July 1976 in “PubMed”

The document's conclusion cannot be provided because the document is not accessible or understandable.

research 0527 Effectiveness of janus kinase inhibitor for rapidly progressive acute alopecia areata

July 2026 in “Journal of Investigative Dermatology”

research Meeting Announcement

January 1997 in “International Society of Hair Restoration Surgery”

research 944 Non-coding double stranded RNA induces retinoic acid synthesis and retinoid signaling to control regeneration

April 2019 in “Journal of Investigative Dermatology”

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

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

60 citations , January 2021 in “BMC Genomics”

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

Correction to: Comparative Study to Evaluate Tolerability of Topical 5% Minoxidil Novel Formulation and Alcohol-Based Conventional Solutions in Treatment of Androgenetic Alopecia in Indian Men: Randomized Double-Blind Study

research Correction to: Comparative Study to Evaluate Tolerability of Topical 5% Minoxidil Novel Formulation and Alcohol-Based Conventional Solutions in Treatment of Androgenetic Alopecia in Indian Men: Randomized Double-Blind Study

April 2020 in “Dermatology and therapy”

research The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata

9 citations , May 2019 in “Medicine”

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

research Association of methionine synthase gene polymorphisms with wool production and quality traits in Chinese Merino population12

17 citations , August 2015 in “Journal of Animal Science”

The MTR gene affects wool quality and production in Chinese Merino sheep.

research Patient welfare

September 2008 in “Hair transplant forum international”

The document's conclusion cannot be determined.

A Case of MBTPS1-Related Disorder Due to Compound Heterozygous Variants in MBTPS1 Gene: Genotype-Phenotype Expansion and the Emergence of a Novel Syndrome

research A case of MBTPS1‐related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype–phenotype expansion and the emergence of a novel syndrome

December 2023 in “American journal of medical genetics. Part A”

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

research PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene

2 citations , May 2023 in “Indian Journal of Dermatology Venereology and Leprology”

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.

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