ADAMTSL4-Related Eye Disorders. PMID: 22338190
The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature. PMID: 36284667
ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent. PMID: 35218299
Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships. PMID: 36208099
ADAMTS proteins in human disorders. PMID: 29885460
Novel ADAMTSL4 gene mutations in Chinese patients with isolated ectopia lentis. PMID: 35042684
ADAMTSL4, a Secreted Glycoprotein, Is a Novel Immune-Related Biomarker for Primary Glioblastoma Multiforme. PMID: 30728876
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians. PMID: 28394649
Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae. PMID: 36089008
Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis. PMID: 35378950
ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis. PMID: 21989719
A de novo variant in the bovine ADAMTSL4 gene in an Original Braunvieh calf with congenital cataract. PMID: 35233794
Focus on molecules: ADAMTSL4. PMID: 22248912
A genotype-phenotype comparison of ADAMTSL4 and FBN1 in isolated ectopia lentis. PMID: 22736615
Molecular Cloning, Lentiviral Transduction, and Expression of Recombinant ADAMTSL2 and ADAMTSL4. PMID: 31463909
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation. PMID: 26405179
ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype description. PMID: 25975359
Typing characteristics of metabolism-related genes in osteoporosis. PMID: 36188607
Role of ADAMTSL4 mutations in FBN1 mutation-negative ectopia lentis patients. PMID: 20564469
A homozygous microdeletion within ADAMTSL4 in patients with isolated ectopia lentis: evidence of a founder mutation. PMID: 21051722
Tumor antigens and immune subtypes of glioblastoma: the fundamentals of mRNA vaccine and individualized immunotherapy development. PMID: 35855914
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin. PMID: 26653794
A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis. PMID: 19200529
A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae. PMID: 20702823
[Hereditary ectopia lentis]. PMID: 25654236
Ectopia Lentis et Pupillae Caused by ADAMTSL4 Pathogenic Variants and an Algorithm for Work-up. PMID: 31282960
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia. PMID: 29346494
Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentis. PMID: 20141359
Ectopia lentis et pupillae in four generations caused by novel mutations in the ADAMTSL4 gene. PMID: 23426735
Novel compound heterozygous mutations identified in ADAMTSL4 gene in a Chinese family with isolated ectopia lentis. PMID: 24802351
Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4. PMID: 22871183
Correlation of five secretory proteins with the nasopharyngeal carcinoma metastasis and the clinical applications. PMID: 28107202
Gene expression and protein distribution of ADAMTSL-4 in human iris, choroid and retina. PMID: 23846871
Identification and validation of a novel senescence-related biomarker for thyroid cancer to predict the prognosis and immunotherapy. PMID: 36761753
ADAMTS proteins as modulators of microfibril formation and function. PMID: 25957949
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yield. PMID: 28642162
The ADAMTS(L) family and human genetic disorders. PMID: 21880666
Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics. PMID: 25770910
Genes associated with diagnosis and prognosis of Burkitt lymphoma. PMID: 36354023
Epidemiology of ectopia lentis and outcomes after surgery in a Danish population. PMID: 36449672
Genetic and functional linkage between ADAMTS superfamily proteins and fibrillin-1: a novel mechanism influencing microfibril assembly and function. PMID: 21858451
Identification of frailty-associated genes by coordination analysis of gene expression. PMID: 32112643
Data-Independent Acquisition-Based Serum Proteomic Profiling of Adult Moyamoya Disease Patients Reveals the Potential Pathogenesis of Vascular Changes. PMID: 36520382
Burden of Rare Genetic Variants in Spontaneous Coronary Artery Dissection With High-risk Features. PMID: 36103205
Single-cell RNA sequencing reveals new subtypes of lens superficial tissue in humans. PMID: 37057399
Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix families. PMID: 29758265
l-Arginine prevents inflammatory and pro-calcific differentiation of interstitial aortic valve cells. PMID: 32169720
Combination of Panel-based Next-Generation Sequencing and Clinical Findings in Congenital Ectopia Lentis Diagnosed in Chinese Patients. PMID: 34818515
The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis. PMID: 37107549
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. PMID: 32887874
The potential prognostic values of the ADAMTS-like protein family: an integrative pan-cancer analysis. PMID: 34790768
Comparison of Pairwise Venous and Fingertip Plasma Using Quantitative Proteomics Based on Data-Independent Acquisition. PMID: 36882937
Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis. PMID: 25053872
OTX2 expression contributes progression of gastric cancer in young adults., PMID:40341176
Genetic landscape and ocular biometric correlations in microspherophakia: insights from a comprehensive patient cohort., PMID:40025527
Ectopia lentis associated with a 20-base deletion in the ADAMTSL4 gene in the Old Order Amish population., PMID:39360343
Mutations in ADAMTSL4 cause a unique form of autosomal-recessive congenital ectopia lentis., PMID:39278391
The Proteomic Landscape of Monocytes in Response to Colorectal Cancer Cells., PMID:39106312
The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease., PMID:38891949
Investigating HMGB1 as a potential serum biomarker for early diabetic nephropathy monitoring by quantitative proteomics., PMID:38303703
Clinical and Genetic Landscape of Ectopia Lentis Based on a Cohort of Patients From 156 Families., PMID:38190127
A novel ADAMTSL4 compound heterozygous mutation in isolated ectopia lentis: a case report and review of the literature., PMID:38146062
Increased plasma expression of a disintegrin and metalloproteinase with thrombospondin motifs like 4 in patients with idiopathic pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension., PMID:37448441
The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis., PMID:37107549
Comparison of Pairwise Venous and Fingertip Plasma Using Quantitative Proteomics Based on Data-Independent Acquisition., PMID:36882937
Data-Independent Acquisition-Based Serum Proteomic Profiling of Adult Moyamoya Disease Patients Reveals the Potential Pathogenesis of Vascular Changes., PMID:36520382
Genes associated with diagnosis and prognosis of Burkitt lymphoma., PMID:36354023
The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literature., PMID:36284667
Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype-phenotype relationships., PMID:36208099
Burden of Rare Genetic Variants in Spontaneous Coronary Artery Dissection With High-risk Features., PMID:36103205
Correlation between novel compound heterozygous ADAMTSL4 variants and primary phenotypes of ectopia lentis et pupillae., PMID:36089008
ADAMTSL4-related ectopia lentis: A case of pseudodominance with an asymptomatic parent., PMID:35218299
Novel ADAMTSL4 gene mutations in Chinese patients with isolated ectopia lentis., PMID:35042684
Combination of Panel-based Next-Generation Sequencing and Clinical Findings in Congenital Ectopia Lentis Diagnosed in Chinese Patients., PMID:34818515
The potential prognostic values of the ADAMTS-like protein family: an integrative pan-cancer analysis., PMID:34790768
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction., PMID:32887874
l-Arginine prevents inflammatory and pro-calcific differentiation of interstitial aortic valve cells., PMID:32169720
Molecular Cloning, Lentiviral Transduction, and Expression of Recombinant ADAMTSL2 and ADAMTSL4., PMID:31463909
Ectopia Lentis et Pupillae Caused by ADAMTSL4 Pathogenic Variants and an Algorithm for Work-up., PMID:31282960
ADAMTSL4, a Secreted Glycoprotein, Is a Novel Immune-Related Biomarker for Primary Glioblastoma Multiforme., PMID:30728876
ADAMTS proteins in human disorders., PMID:29885460
Interactions between lysyl oxidases and ADAMTS proteins suggest a novel crosstalk between two extracellular matrix families., PMID:29758265
Next-generation sequencing reveals a new mutation in the LTBP2 gene associated with microspherophakia in a Spanish family., PMID:29751740
Human Properdin Opsonizes Nanoparticles and Triggers a Potent Pro-inflammatory Response by Macrophages without Involving Complement Activation., PMID:29483907
Novel Myopia Genes and Pathways Identified From Syndromic Forms of Myopia., PMID:29346494
Identification of a t(3;4)(p1.3;q1.5) translocation breakpoint in pigs using somatic cell hybrid mapping and high-resolution mate-pair sequencing., PMID:29121641
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yield., PMID:28642162
ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians., PMID:28394649
Correlation of five secretory proteins with the nasopharyngeal carcinoma metastasis and the clinical applications., PMID:28107202
A founder mutation in ADAMTSL4 causes early-onset bilateral ectopia lentis among Jews of Bukharian origin., PMID:26653794
Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation., PMID:26405179
ADAMTSL4-associated isolated ectopia lentis: Further patients, novel mutations and a detailed phenotype description., PMID:25975359
ADAMTS proteins as modulators of microfibril formation and function., PMID:25957949
Insights on ADAMTS proteases and ADAMTS-like proteins from mammalian genetics., PMID:25770910
[Hereditary ectopia lentis]., PMID:25654236
Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis., PMID:25053872
Novel compound heterozygous mutations identified in ADAMTSL4 gene in a Chinese family with isolated ectopia lentis., PMID:24802351
Gene expression and protein distribution of ADAMTSL-4 in human iris, choroid and retina., PMID:23846871
Ectopia lentis et pupillae in four generations caused by novel mutations in the ADAMTSL4 gene., PMID:23426735
Versican processing by a disintegrin-like and metalloproteinase domain with thrombospondin-1 repeats proteinases-5 and -15 facilitates myoblast fusion., PMID:23233679
Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4., PMID:22871183
A genotype-phenotype comparison of ADAMTSL4 and FBN1 in isolated ectopia lentis., PMID:22736615
For research use only. Not for human or drug use.
