Qiaoli Li

发表

Functional analysis of rice NPR1-like genes reveals that OsNPR1/NH1 is the rice orthologue conferring disease resistance with enhanced herbivore susceptibility.

Jianjun Wang, Yuexing Yuan, Sihui Zhong, 2007, Plant biotechnology journal.

Analysis of Pseudoxanthoma Elasticum-Causing Missense Mutants of ABCC6 in vivo; Pharmacological Correction of the Mislocalized Proteins

J. Uitto, Qiaoli Li, A. Váradi, 2013, The Journal of investigative dermatology.

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

B. Li, E. Nogales, Mohan L Gupta, 2016, The New England journal of medicine.

Dynamics and Emerging Trends in Genodermatology: A Scientometric Analysis

J. Uitto, Qiaoli Li, Liangyong Zhou, 2021, International Journal of Dermatology and Venereology.

High Expression of DC-STAMP Gene Predicts Adverse Outcomes in AML

Qiaoli Li, Zhen Gao, Q. Liang, 2022, Frontiers in Genetics.

Virucidal activity of a scorpion venom peptide variant mucroporin-M1 against measles, SARS-CoV and influenza H5N1 viruses

Z. Cao, Yingliang Wu, Wen-xin Li, 2011, Peptides.

Anti-HIV-1 Activity of a New Scorpion Venom Peptide Derivative Kn2-7

Fang Liu, Yan Zhang, Wenxin Li, 2012, PloS one.

Common genetic variation in CYP1B1 is associated with concentrations of T4, FT3 and FT4 in the sera of polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2013, Molecular Biology Reports.

Changes in dermal fibroblasts from Abcc6−/− mice are present before and after the onset of ectopic tissue mineralization

J. Uitto, Qiaoli Li, D. Quaglino, 2014, The Journal of investigative dermatology.

Morphology and stability changes of recombinant TMV particles caused by a cysteine residue in the foreign peptide fused to the coat protein.

Zhengkai Xu, R. Song, Mangmang Li, 2007, Journal of virological methods.

Atherogenic Diet Accelerates Ectopic Mineralization in a Mouse Model of Pseudoxanthoma Elasticum

J. Uitto, Qiaoli Li, Jingyi Zhao, 2020, International journal of dermatology and venereology.

Case Report: The Experience of Managing a Moderate ARDS Caused by SARS-CoV-2 Omicron BA.2 Variant in Chongqing, China: Can We Do Better?

Qiaoli Li, Dao-xin Wang, Jing Dong, 2022, Frontiers in Medicine.

Unraveling most abundant mutational signatures in head and neck cancer

W. Weichert, K. Zaoui, K. Freier, 2020, International journal of cancer.

Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.

S. Terry, P. Fortina, J. Uitto, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Vascular Mineralization in Pseudoxanthoma Elasticum: Etidronate to the Rescue?

J. Uitto, Qiaoli Li, 2018, Journal of the American College of Cardiology.

Elevated dietary magnesium during pregnancy and postnatal life prevents ectopic mineralization in Enpp1asj mice, a model for generalized arterial calcification of infancy

J. Uitto, Qiaoli Li, J. Kingman, 2017, Oncotarget.

Research Progress in Pseudoxanthoma Elasticum and Related Ectopic Mineralization Disorders

S. Terry, J. Uitto, T. Arányi, 2015, The Journal of investigative dermatology.

Ectopic mineralization of cartilage and collagen-rich tendons and ligaments in Enpp1asj-2J mice

J. Sundberg, J. Uitto, D. Rowe, 2016, Oncotarget.

Mineral content of the maternal diet influences ectopic mineralization in offspring of Abcc6−/− mice

J. Uitto, Qiaoli Li, J. Kingman, 2015, Cell cycle.

The effects of bisphosphonates on ectopic soft tissue mineralization caused by mutations in the ABCC6 gene

S. Terry, J. Sundberg, J. Uitto, 2015, Cell cycle.

Ectopic mineralization disorders of the extracellular matrix of connective tissue: molecular genetics and pathomechanisms of aberrant calcification.

J. Uitto, Qiaoli Li, Qiujie Jiang, 2014, Matrix biology : journal of the International Society for Matrix Biology.

Warfarin accelerates ectopic mineralization in Abcc6(-/-) mice: clinical relevance to pseudoxanthoma elasticum.

S. Terry, J. Uitto, L. Schurgers, 2013, The American journal of pathology.

Mineralization/anti-mineralization networks in the skin and vascular connective tissues.

J. Uitto, Qiaoli Li, 2013, The American journal of pathology.

Atorvastatin counteracts aberrant soft tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6−/−)

J. Uitto, Qiaoli Li, Haitao Guo, 2013, Journal of Molecular Medicine.

Up-Regulated Expression and Aberrant DNA Methylation of LEP and SH3PXD2A in Pre-Eclampsia

Yun Liu, Qiaoli Li, Xiaotian Li, 2013, PloS one.

Epidemiologic, Clinicopathologic, Diagnostic, and Management Challenges of Pityriasis Rubra Pilaris: A Case Series of 100 Patients.

J. Uitto, Qiaoli Li, M. Keller, 2016, JAMA dermatology.

Genetic variations in the 3'-untranslated region of SLC18A2 are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expression in vitro.

Qiaoli Li, Y. Kuang, Zheng Yan, 2016, Human reproduction.

A possible new mechanism in the pathophysiology of polycystic ovary syndrome (PCOS): the discovery that leukocyte telomere length is strongly associated with PCOS.

Qiaoli Li, Q. Xing, Ruizhi Feng, 2014, The Journal of clinical endocrinology and metabolism.

Targeted ablation of Abcc1 or Abcc3 in Abcc6−/− mice does not modify the ectopic mineralization process

J. Uitto, J. F. Klement, A. Sartorelli, 2007, Experimental dermatology.

Pseudoxanthoma elasticum: oxidative stress and antioxidant diet in a mouse model (Abcc6-/-).

J. Uitto, Qiaoli Li, Qiujie Jiang, 2008, The Journal of investigative dermatology.

Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42.

Shan Sun, Dong Liu, R. Chai, 2014, Human molecular genetics.

Ildr 1 b is essential for semicircular canal development , migration of the posterior lateral line primordium and hearing ability in zebrafish : implications for a role in the recessive hearing impairment DFNB 42

Shan Sun, Dong Liu, R. Chai, 2014 .

Quantitative Trait Locus and Integrative Genomics Revealed Candidate Modifier Genes for Ectopic Mineralization in Mouse Models of Pseudoxanthoma Elasticum.

J. Sundberg, M. Wiles, J. Uitto, 2019, The Journal of investigative dermatology.

Trauma-Induced Nanohydroxyapatite Deposition in Skeletal Muscle is Sufficient to Drive Heterotopic Ossification

J. Uitto, H. Schwartz, J. Cates, 2018, Calcified Tissue International.

Therapeutics Development for Pseudoxanthoma Elasticum and Related Ectopic Mineralization Disorders: Update 2020

J. Uitto, Qiaoli Li, Yi Cao, 2020, Journal of clinical medicine.

Adenovirus-Mediated ABCC6 Gene Therapy for Heritable Ectopic Mineralization Disorders.

J. Uitto, Qiaoli Li, Jianhe Huang, 2019, The Journal of investigative dermatology.

TMV recombinants encoding fused foreign transmembrane domains to the CP subunit caused local necrotic response on susceptible tobacco

Zhengkai Xu, R. Song, Mangmang Li, 2006, Virology.

Molecular Genetics and Modifier Genes in Pseudoxanthoma Elasticum, a Heritable Multisystem Ectopic Mineralization Disorder.

J. Uitto, Qiaoli Li, Yi Cao, 2020, The Journal of investigative dermatology.

A novel animal model for pseudoxanthoma elasticum: the KK/HlJ mouse.

J. Sundberg, J. Uitto, Qiaoli Li, 2012, The American journal of pathology.

Pseudoxanthoma elasticum: the paradigm of ectopic mineralization disorders – diagnosis and treatment

J. Uitto, Qiaoli Li, Qiujie Jiang, 2013 .

Inhibition of the DNA Damage Response Attenuates Ectopic Calcification in Pseudoxanthoma Elasticum.

J. Uitto, Qiaoli Li, D. Quaglino, 2022, The Journal of investigative dermatology.

Ectopic mineralization of connective tissue in Abcc6–/– mice: effects of dietary modifications and a phosphate binder – a preliminary study

J. Uitto, Qiaoli Li, Qiujie Jiang, 2008, Experimental dermatology.

Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma

J. Uitto, Qiaoli Li, G. Richard, 2022, Human mutation.

Zebrafish as a model system to study heritable skin diseases.

J. Uitto, Qiaoli Li, 2013, Methods in molecular biology.

Zebrafish: a model system to study heritable skin diseases.

J. Uitto, B. Thisse, C. Thisse, 2011, The Journal of investigative dermatology.

Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia.

Qiaoli Li, Xiaotian Li, Yuqian Xiang, 2011, Molecular human reproduction.

The complexity of elastic fibre biogenesis in the skin – a perspective to the clinical heterogeneity of cutis laxa

J. Uitto, Qiaoli Li, Z. Urban, 2013, Experimental dermatology.

Curative Effect of Prebiotics/Probiotics Preparations Combined with Zoledronic Acid + Calcitriol Regimen on Patients with Primary Osteoporosis and Their Influences on Bone Metabolism Markers

Qiaoli Li, Ruipeng Jia, Ning-jiang Liu, 2022, Emergency medicine international.

Inorganic pyrophosphate deficiency syndromes and potential treatments for pathologic tissue calcification.

J. Uitto, Qiaoli Li, K. van de Wetering, 2022, The American journal of pathology.

Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest.

Ling Wu, Qiaoli Li, Y. Kuang, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Analysis of JAG1 gene variant in Chinese patients with Alagille syndrome.

Yun Liu, Xiaohong Wang, Qiaoli Li, 2012, Gene.

Zebrafish type XVII collagen: gene structures, expression profiles, and morpholino "knock-down" phenotypes.

Cheol‐Hee Kim, J. Uitto, Qiaoli Li, 2010, Matrix biology : journal of the International Society for Matrix Biology.

Magnesium Reduces Carotid Intima‐Media Thickness in a Mouse Model of Pseudoxanthoma Elasticum: A Novel Treatment Biomarker

J. Uitto, Qiaoli Li, E. A. Kupetsky-Rincon, 2012, Clinical and translational science.

Loci with genome-wide associations with schizophrenia in the Han Chinese population.

Lin He, Jiawei Shen, Yongyong Shi, 2015, The British journal of psychiatry : the journal of mental science.

Mouse Models for Pseudoxanthoma Elasticum: Genetic and Dietary Modulation of the Ectopic Mineralization Phenotypes

J. Sundberg, J. Uitto, Qiaoli Li, 2014, PloS one.

Mouse Alopecia Areata and Heart Disease: Know Your Mouse!

J. Sundberg, J. Uitto, Qiaoli Li, 2013, The Journal of investigative dermatology.

A single nucleotide polymorphism in the Abcc6 gene associates with connective tissue mineralization in mice similar to targeted models for pseudoxanthoma elasticum

J. Sundberg, J. Uitto, Qiaoli Li, 2012, The Journal of investigative dermatology.

A novel splicing variant in DNAH8 causes asthenozoospermia

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Journal of Assisted Reproduction and Genetics.

Pseudoxanthoma elasticum: reduced gamma-glutamyl carboxylation of matrix gla protein in a mouse model (Abcc6-/-).

J. Uitto, L. Schurgers, Qiaoli Li, 2007, Biochemical and biophysical research communications.

Zebrafish Models of Ectopic Mineralization-The Paradigm of Pseudoxanthoma Elasticum.

J. Uitto, Qiaoli Li, 2018, The Journal of investigative dermatology.

Zebrafish as a model system to study skin biology and pathology.

J. Uitto, Qiaoli Li, 2014, The Journal of investigative dermatology.

Promoter hypomethylation of TIMP3 is associated with pre-eclampsia in a Chinese population.

Yun Liu, Qiaoli Li, Yuqian Xiang, 2013, Molecular human reproduction.

Matrix Protein-Specific IgA Antibody Inhibits Measles Virus Replication by Intracellular Neutralization

L. Lei, D. Zhou, Jingyi Yang, 2011, Journal of Virology.

Recombinant flagellins with partial deletions of the hypervariable domain lose antigenicity but not mucosal adjuvancy.

P. Tien, D. Zhou, Jingyi Yang, 2010, Biochemical and biophysical research communications.

Administration of vitamin K does not counteract the ectopic mineralization of connective tissues in Abcc6-/- mice, a model for pseudoxanthoma elasticum

J. Uitto, L. Schurgers, Qiaoli Li, 2011, Cell cycle.

Fibroadipose hyperplasia versus Proteus syndrome: segmental overgrowth with a mosaic mutation in the PIK3CA gene.

J. Uitto, Qiaoli Li, H. Vahidnezhad, 2015, The Journal of investigative dermatology.

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

S. Terry, J. Uitto, Qiaoli Li, 2022, PLoS genetics.

The pathogenic c.1171A>G (p.Arg391Gly) and c.2359G>A (p.Val787Ile) ABCC6 variants display incomplete penetrance causing pseudoxanthoma elasticum in a subset of individuals

S. Terry, K. Tory, J. Uitto, 2022, Human mutation.

Aberrant mineralization of connective tissues in a mouse model of pseudoxanthoma elasticum: systemic and local regulatory factors.

J. Uitto, Qiaoli Li, Qiujie Jiang, 2007, The Journal of investigative dermatology.

ABCC6 does not transport adenosine - relevance to pathomechanism of pseudoxanthoma elasticum.

J. Uitto, Qiaoli Li, A. Váradi, 2011, Molecular genetics and metabolism.

Co-existent pseudoxanthoma elasticum and vitamin K-dependent coagulation factor deficiency: compound heterozygosity for mutations in the GGCX gene.

J. Uitto, L. Schurgers, M. Tsokos, 2009, The American journal of pathology.

Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.

Ling Wu, Qiaoli Li, Y. Kuang, 2018, American journal of human genetics.

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest

Ling Wu, Qiaoli Li, Y. Kuang, 2019, Journal of Medical Genetics.

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.

Zhaogui Sun, Qiaoli Li, Suying Liu, 2018, Reproductive biomedicine online.

Dual Effects of Bisphosphonates on Ectopic Skin and Vascular Soft Tissue Mineralization versus Bone Microarchitecture in a Mouse Model of Generalized Arterial Calcification of Infancy

J. Sundberg, J. Uitto, Qiaoli Li, 2015, The Journal of investigative dermatology.

Spontaneous asj-2J Mutant Mouse as a Model for Generalized Arterial Calcification of Infancy: A Large Deletion/Insertion Mutation in the Enpp1 Gene

J. Sundberg, J. Uitto, Qiaoli Li, 2014, PloS one.

Etidronate prevents, but does not reverse, ectopic mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6-/-).

J. Sundberg, J. Uitto, Qiaoli Li, 2014, Oncotarget.

Genetic modulation of nephrocalcinosis in mouse models of ectopic mineralization: The Abcc6tm1Jfk and Enpp1asj mutant mice

J. Sundberg, J. Uitto, Qiaoli Li, 2014, Laboratory Investigation.

Calpain 12 Function Revealed through the Study of an Atypical Case of Autosomal Recessive Congenital Ichthyosis.

O. Sarig, G. Ast, N. Shomron, 2016, The Journal of investigative dermatology.

Extending the Phenotypic Spectrum of Keratitis‐Ichthyosis‐Deafness Syndrome: Report of a Patient with GJB2 (G12R) Connexin 26 Mutation and Unusual Clinical Findings

J. Uitto, Qiaoli Li, L. Zhou, 2012, Pediatric dermatology.

The aberrantly expressed miR-193b-3p contributes to preeclampsia through regulating transforming growth factor-β signaling

Qiaoli Li, Yuqian Xiang, Mingqing Xu, 2016, Scientific Reports.

Connective tissue mineralization in Abcc6-/- mice, a model for pseudoxanthoma elasticum.

J. Uitto, N. Pleshko, Qiaoli Li, 2012, Matrix biology : journal of the International Society for Matrix Biology.

Pseudoxanthoma elasticum: clinical phenotypes, molecular genetics and putative pathomechanisms

J. Uitto, Qiaoli Li, A. Váradi, 2009, Experimental dermatology.

Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy – Genotypic Overlap with Pseudoxanthoma Elasticum

H. Hakonarson, J. Uitto, L. Schurgers, 2013, The Journal of investigative dermatology.

Magnesium Carbonate‐Containing Phosphate Binder Prevents Connective Tissue Mineralization in Abcc6−/− Mice–Potential for Treatment of Pseudoxanthoma Elasticum

J. Uitto, Qiaoli Li, Jennifer Larusso, 2009, Clinical and translational science.

Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1

J. Uitto, S. Akhondzadeh, Qiaoli Li, 2015, Experimental dermatology.

Cole Disease Results from Mutations in ENPP1.

O. Sarig, N. Shomron, J. Uitto, 2013, American journal of human genetics.

A pannexin 1 channelopathy causes human oocyte death

Ling Wu, Qiang Sun, Qiaoli Li, 2019, Science Translational Medicine.

Mutant Enpp1asj mice as a model for generalized arterial calcification of infancy

J. Sundberg, J. Uitto, Qiaoli Li, 2013, Disease Models & Mechanisms.

Inhibition of Tissue-Nonspecific Alkaline Phosphatase Attenuates Ectopic Mineralization in the Abcc6-/- Mouse Model of PXE but Not in the Enpp1 Mutant Mouse Models of GACI.

J. Sundberg, J. Uitto, J. Millán, 2019, The Journal of investigative dermatology.

Anti-HIV-1 Activity of a New Scorpion Venom Peptide Derivative Kn 2-7

Jie Yu, M. Zhong, D. Zhou, 2012 .

LncRNA DBH-AS1 facilitates the tumorigenesis of hepatocellular carcinoma by targeting miR-138 via FAK/Src/ERK pathway.

Qiaoli Li, Xiaoqi Chen, Yun Xu, 2018, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Frontiers in Cell and Developmental Biology.

Homozygous variants in PANX1 cause human oocyte death and female infertility

Qiaoli Li, Qing Sang, Ronggui Qu, 2021, European Journal of Human Genetics.

Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Protein & Cell.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

Novel mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development

Qiaoli Li, Da Li, Y. Kuang, 2017, Human reproduction.

Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.

Ling Wu, Qiaoli Li, Da Li, 2021, Human reproduction.

Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest

Ling Wu, Qiaoli Li, Y. Kuang, 2019, Journal of Medical Genetics.

Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Journal of Assisted Reproduction and Genetics.

Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest.

Qiaoli Li, Y. Kuang, Zheng Yan, 2017, American journal of human genetics.

Analysis of CARD14 Polymorphisms in Pityriasis Rubra Pilaris: Activation of NF-κB

O. Sarig, J. Uitto, E. Sprecher, 2015, The Journal of investigative dermatology.

Quantitative analysis of follistatin (FST) promoter methylation in peripheral blood of patients with polycystic ovary syndrome.

Huan Wang, Qiaoli Li, Q. Xing, 2013, Reproductive biomedicine online.

The abcc6a gene expression is required for normal zebrafish development.

J. Uitto, M. Dean, B. Thisse, 2010, The Journal of investigative dermatology.

The pathogenic p.(R391G) ABCC6 displays incomplete penetrance implying the necessity of an interacting partner for the development of pseudoxanthoma elasticum

S. Terry, K. Tory, J. Uitto, 2020, medRxiv.

Lack of support for association between the copy number variants in the FCGR locus and schizophrenia: A case control study

Yun Liu, Qiaoli Li, G. Feng, 2012, Neuroscience Letters.

SVEP1 plays a crucial role in epidermal differentiation

O. Sarig, J. Uitto, E. Sprecher, 2017, Experimental dermatology.

Elevated dietary magnesium prevents connective tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6(-/-)).

J. Uitto, Qiaoli Li, Qiujie Jiang, 2009, The Journal of investigative dermatology.

Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis

J. Uitto, E. Sprecher, T. Inaba, 2012, Experimental dermatology.

The Samd9L gene: transcriptional regulation and tissue-specific expression in mouse development.

J. Uitto, E. Sprecher, T. Inaba, 2011, The Journal of investigative dermatology.

Detection of Turner syndrome using X-chromosome inactivation specific differentially methylated CpG sites: A pilot study.

Yun Liu, Qiaoli Li, Q. Xing, 2017, Clinica chimica acta; international journal of clinical chemistry.

Pseudoxanthoma elasticum: molecular genetics and putative pathomechanisms.

J. Uitto, Qiaoli Li, Qiujie Jiang, 2010, The Journal of investigative dermatology.

Unpolarized Release of Vaccinia Virus and HIV Antigen by Colchicine Treatment Enhances Intranasal HIV Antigen Expression and Mucosal Humoral Responses

Jingyi Yang, M. Zhong, D. Zhou, 2011, PloS one.

The abcc6a Gene is Required for Normal Zebrafish Development

J. Uitto, B. Thisse, C. Thisse, 2012 .

A modified TMV-based vector facilitates the expression of longer foreign epitopes in tobacco.

Zhengkai Xu, Mangmang Li, Qiaoli Li, 2006, Vaccine.

INZ‐701, a recombinant ENPP1 enzyme, prevents ectopic calcification in an Abcc6−/− mouse model of pseudoxanthoma elasticum

J. Uitto, K. O'Brien, Qiaoli Li, 2022, Experimental dermatology.

Oral supplementation of inorganic pyrophosphate in pseudoxanthoma elasticum

S. Terry, J. Uitto, N. Tőkési, 2021, Experimental dermatology.

Functional Assessment of Missense Variants in the ABCC6 gene Implicated in Pseudoxanthoma Elasticum, a Heritable Ectopic Mineralization Disorder.

J. Uitto, Qiaoli Li, Jianhe Huang, 2021, The Journal of investigative dermatology.

A phytic acid analogue INS‐3001 prevents ectopic calcification in an Abcc6−/− mouse model of pseudoxanthoma elasticum

J. Uitto, Qiaoli Li, Diana Li, 2021, Experimental dermatology.

Plasma PPi Deficiency Is the Major, but Not the Exclusive, Cause of Ectopic Mineralization in an Abcc6-/- Mouse Model of PXE.

J. Sundberg, J. Uitto, Qiaoli Li, 2017, The Journal of investigative dermatology.

Abcc6 Knockout Rat Model Highlights the Role of Liver in PPi Homeostasis in Pseudoxanthoma Elasticum.

J. Uitto, Qiaoli Li, K. van de Wetering, 2017, The Journal of investigative dermatology.

Clinical and histopathological characteristics of a family with R1141X mutation of pseudoxanthoma elasticum - presymptomatic testing and lack of carrier phenotypes.

J. Uitto, Qiaoli Li, G. Akoglu, 2014, International journal of dermatology.

Heritable ectopic mineralization disorders: the paradigm of pseudoxanthoma elasticum.

J. Uitto, Qiaoli Li, 2012, The Journal of investigative dermatology.

Pseudoxanthoma elasticum, the paradigm of heritable ectopic mineralization disorders – can diet help?

J. Uitto, Qiaoli Li, Jennifer Larusso, 2011, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypes.

Nicole L. Armstrong, J. Uitto, L. Schurgers, 2009, The Journal of investigative dermatology.

Juxta-articular joint-capsule mineralization in CD73 deficient mice: Similarities to patients with NT5E mutations

J. Sundberg, J. Uitto, Qiaoli Li, 2014, Cell cycle.

DNA methylome profiling of maternal peripheral blood and placentas reveal potential fetal DNA markers for non-invasive prenatal testing.

Qiaoli Li, Yuqian Xiang, Mingqing Xu, 2014, Molecular human reproduction.

Pseudoxanthoma Elasticum as a Paradigm of Heritable Ectopic Mineralization Disorders: Pathomechanisms and Treatment Development.

J. Uitto, Qiaoli Li, K. van de Wetering, 2019, The American journal of pathology.

Etidronate prevents, but does not reverse, ectopic mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6−/−)

J. Sundberg, J. Uitto, Qiaoli Li, 2018, Oncotarget.

Insights into Pathomechanisms and Treatment Development in Heritable Ectopic Mineralization Disorders: Summary of the PXE International Biennial Research Symposium-2016.

S. Terry, J. Uitto, Qiaoli Li, 2017, The Journal of investigative dermatology.

Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis

J. Sundberg, J. Uitto, P. Schofield, 2016, Mammalian Genome.

Atorvastatin counteracts aberrant soft tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6−/−)

J. Uitto, Qiaoli Li, Haitao Guo, 2013, Journal of molecular medicine.

Expression of the Abca‐subfamily of genes in Abcc6−/− mice – upregulation of Abca4

J. Uitto, Qiaoli Li, 2011, Experimental dermatology.

Prenatal Nutritional Deficiency Reprogrammed Postnatal Gene Expression in Mammal Brains: Implications for Schizophrenia

Jingde Zhu, G. He, D. St. Clair, 2015, The international journal of neuropsychopharmacology.

ABC Transporter Mutations in Heritable Skin Diseases: The ABCC6 and ABCA12 Genes

J. Uitto, Qiaoli Li, Qiujie Jiang, 2011 .

The mineralization phenotype in Abcc6−/− mice is affected by Ggcx gene deficiency and genetic background—a model for pseudoxanthoma elasticum

J. Uitto, Qiaoli Li, 2010, Journal of Molecular Medicine.

Abca12-mediated lipid transport and Snap29-dependent trafficking of lamellar granules are crucial for epidermal morphogenesis in a zebrafish model of ichthyosis

M. Akiyama, H. Shimizu, J. Uitto, 2011, Disease Models & Mechanisms.

The DNA methylation status of genes encoding Matrix metalloproteinases and tissue inhibitors of Matrix metalloproteinases in endometriosis

Qiaoli Li, Yuqian Xiang, Q. Xing, 2018, Molecular reproduction and development.

Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects

Ling Wu, Qiaoli Li, Juan-zi Shi, 2023, Genome Biology.

Weighing the Evidence for the Roles of Plasma Versus Local Pyrophosphate in Ectopic Calcification Disorders

J. Uitto, J. Millán, Qiaoli Li, 2023, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.

J. Uitto, S. Zeinali, Qiaoli Li, 2015, The Journal of investigative dermatology.

ADGB variants cause asthenozoospermia and male infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2023, Human Genetics.

Comparison of 1D and 2D NMR spectroscopy for metabolic profiling.

Jouni Uitto, Timothy D Veenstra, Michael Dean, 2008, Journal of proteome research.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

FBXO43 variants in patients with female infertility characterized by early embryonic arrest.

Qiaoli Li, Juan-zi Shi, Qing Sang, 2021, Human reproduction.

A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.

Huan Wang, Qiaoli Li, Q. Xing, 2011, Molecular human reproduction.

A FBN1 mutation association with different phenotypes of Marfan syndrome in a Chinese family.

Yapeng Li, Yanzhou Zhang, Qiaoli Li, 2016, Clinica chimica acta; international journal of clinical chemistry.

High-expression of the innate-immune related gene UNC93B1 predicts inferior outcomes in acute myeloid leukemia

Weiping Yuan, Qiaoli Li, Lele Zhang, 2023, Frontiers in Genetics.

Common genetic variation in CYP1B1 is associated with concentrations of T4, FT3 and FT4 in the sera of polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2013, Molecular Biology Reports.

Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients

Huan Wang, Qiaoli Li, Q. Xing, 2011, Human Genetics.

Kidney Stones Are Prevalent in Individuals with Pseudoxanthoma Elasticum, a Genetic Ectopic Mineralization Disorder

S. Terry, J. Uitto, Qiaoli Li, 2020 .

Spontaneous asj-2 J Mutant Mouse as a Model for Generalized Arterial Calcification of Infancy : A Large Deletion / Insertion Mutation in the Enpp 1 Gene

J. Sundberg, J. Uitto, Qiaoli Li, 2018 .

A novel homozygous missense variant in BTG4 causes zygotic cleavage failure and female infertility

Qiaoli Li, Yifan Zhou, Qing Sang, 2021, Journal of Assisted Reproduction and Genetics.

Reply to Van Gils and Vanakker.

J. Uitto, Qiaoli Li, 2019, The Journal of investigative dermatology.

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

Huan Wang, Duan Ma, Huawei Li, 2013, PloS one.

Trauma-Induced Nanohydroxyapatite Deposition in Skeletal Muscle is Sufficient to Drive Heterotopic Ossification

J. Uitto, H. Schwartz, J. Cates, 2018, Calcified Tissue International.

potential fetal DNA markers for noninvasive prenatal testing

Qiaoli Li, Yuqian Xiang, Mingqing Xu, 2014 .

Quantitative Methylation Level of the EPHX1 Promoter in Peripheral Blood DNA Is Associated with Polycystic Ovary Syndrome

Huan Wang, Qiaoli Li, Q. Xing, 2014, PloS one.

Karyopherin α deficiency contributes to human preimplantation embryo arrest

Ling Wu, Y. Miyamoto, Qiaoli Li, 2023, The Journal of clinical investigation.

Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility

Qiaoli Li, Juan-zi Shi, Qing Sang, 2023, EMBO molecular medicine.

GGCX mutations in a patient with PXE/CL-like overlapping phenotype.

S. Terry, J. Uitto, N. Haass, 2020, The British journal of dermatology.

Next-generation sequencing for mutation detection in heritable skin diseases: the paradigm of pseudoxanthoma elasticum.

J. Uitto, Qiaoli Li, A. South, 2015, The Journal of investigative dermatology.

Paediatric pseudoxanthoma elasticum with cardiovascular involvement

J. Uitto, Qiaoli Li, L. Schachner, 2013, The British journal of dermatology.

Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene

J. Uitto, D. Siegel, Qiaoli Li, 2012, The British journal of dermatology.

Angioid streaks in Pseudoxanthoma Elasticum: role of the p.R1268Q mutation in the ABCC6 gene.

J. Uitto, Qiaoli Li, S. Sadowski, 2011, The Journal of investigative dermatology.

airway responsiveness in inbred mice forced oscillation for identifying genetic variability of Comparison of unrestrained plethysmography and

K. Svenson, J. Sundberg, R. Bronson, 2015 .