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research Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review

1 citations , May 2023 in “Frontiers in Pharmacology”

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

research POST-COVID 19 ENCEPHALITIS IN PATIENT WITH DE NOVO MUTATION IN THE SCN1A GENE, A CASE REPORT

March 2022 in “Piretc”

A person with a new mutation in the SCN1A gene developed brain inflammation after COVID-19.

research Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles

August 2022 in “Frontiers in genetics”

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

research A Homozygous Frameshift Mutation in theHOXC13Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family

30 citations , January 2013 in “Human Mutation”

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

research MINOXIDIL INDUCED PLEURO-PERICARDIAL EFFUSION IN END-STAGE RENAL DISEASE

1 citations , March 2023 in “Journal of the American College of Cardiology”

ISHRS: Expanding Follicular Unit Extraction Education

research ISHRS: Expanding FUE Education

November 2015 in “Hair transplant forum international”

The document's conclusion cannot be provided as the content is not available to parse.

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.

The Free Communications of the Eighth Clinical Congress (Virtual) of the Gulf Chapter of the American Association of Clinical Endocrinologists; November 5–7, 2020

research The Free Communications of the Eighth Clinical Congress (Virtual) of the Gulf Chapter of the American Association of Clinical Endocrinologists; November 5–7, 2020

1 citations , December 2020 in “Journal of diabetes and endocrine practice”

I'm sorry, but I can't provide a summary without the content of the document.

research The role of the androgen receptor gene CAG repeat polymorphism and X-chromosome inactivation pattern in postmenopausal female pattern hair loss

2 citations , January 2008 in “Oxford University Research Archive (ORA) (University of Oxford)”

research The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations

1 citations , June 2022 in “Journal of Cosmetic Dermatology”

Two specific genetic markers increase the risk of hair loss in Asian populations.

research Surgical Assistant’s Pearl on Graft Cutting

November 2007 in “Hair transplant forum international”

The document's conclusion cannot be provided because the content is not available to parse.

research Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women

15 citations , January 2010 in “Reproduction, Fertility and Development”

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

research Clinical Snippets

June 2005 in “Journal of Investigative Dermatology”

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

research Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement

May 2026 in “Frontiers in Medicine”

The patient's hair improved after treatment, but the genetic link is unclear.

research Abstract P35

February 2014 in “Plastic and Reconstructive Surgery”

I'm sorry, but I can't provide a summary as no specific information or context was given in your request.

Complete Defect in PA-PLA1α Secretion Function Leading to Autosomal Recessive Woolly Hair and Hypotrichosis: Insights from a Novel Compound Heterozygous LIPH Variant Study in a Chinese Pedigree

research Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree

May 2025 in “Frontiers in Genetics”

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

research Free Information about Follicular Unit Transplantation

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

research Table S1. Disease-dependent differences between tape-strip and bulk biopsy ssGSEA scores across hair follicle compartments

January 2026 in “Figshare”

research Table S1. Disease-dependent differences between tape-strip and bulk biopsy ssGSEA scores across hair follicle compartments

January 2026 in “Figshare”

A Newly Identified Missense Mutation of the HR Gene Is Associated with a Novel, Unusual Phenotype of Marie Unna Hereditary Hypotrichosis 1 Including Limb Deformities

research A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities

6 citations , May 2012 in “Archives of Dermatological Research”

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

research Atualização em Coriorretinopatia Serosa Central

January 2016 in “e-Oftalmo CBO Revista Digital de Oftalmologia”

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

research Characterization and functional analysis of Krtap11-1 during hair follicle development in Angora rabbits (Oryctolagus cuniculus)

8 citations , September 2020 in “Genes & Genomics”

research A phase I study of MK-5108, an oral aurora A kinase inhibitor, in both monotherapy and in combination with docetaxel in patients with advanced solid tumors.

12 citations , May 2010 in “Journal of Clinical Oncology”

MK-5108 is safe and shows potential against tumors, especially alone.

Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners

research Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.

January 1999 in “American Journal of Medical Genetics Part A”

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

research 0196 Levamisole-induced pyoderma gangrenosum case report

1 citations , July 2025 in “Journal of Investigative Dermatology”

research Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population

3 citations , October 2021 in “The Application of Clinical Genetics”

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

research ROBERTSONIAN TRANSLOCATION PATIENT WITH RECURRENT MISCARRIAGE

June 2020 in “Zenodo (CERN European Organization for Nuclear Research)”

Robertsonian translocation can cause recurrent miscarriages.

research The Columbia Manual of Dermatologic Cosmetic Surgery

2 citations , February 2002

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

Safety, Tolerability, and Pharmacokinetics of CG2001 in Chinese Adult Male Subjects With Androgenetic Alopecia: A Randomized, Double-Blind, Placebo-Controlled, Single- and Multi-Dose, Phase 1 Clinical Study

research Safety, tolerability, and pharmacokinetics of CG2001 in Chinese adult male subjects with androgenetic alopecia: a randomized, double-blind, placebo-controlled, single- and multi-doses, phase 1 clinical study

January 2026

CG2001 is safe and well-tolerated for treating hair loss in men.

research Laser-Guided Hairline Design and Donor Strip Marking

4 citations , March 2007 in “Hair transplant forum international”

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

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