Adamts18 Deficiency Causes Spontaneous SMG Fibrogenesis in Adult Mice

The secreted protease Adamts18 links hormone action to activation of the mammary stem cell niche

(2020) Dalya Ataca et al.   Nature Communications

ADAMTS18 Deficiency Leads to Pulmonary Hypoplasia and Bronchial Microfibril Accumulation

(2020) Tiantian Lu et al.   iScience

Morphogenesis of the kidney and lung requires branch-tip directed activity of the Adamts18 metalloprotease

(2019) Elisabeth A. Rutledge et al.   DEVELOPMENTAL BIOLOGY

Salivary lipids: A review

(2017) Jan Matczuk et al.   Advances in Clinical and Experimental Medicine

Adamts18 deficiency promotes colon carcinogenesis by enhancing β-catenin and p38MAPK/ERK1/2 signaling in the mouse model of AOM/DSS-induced colitis-associated colorectal cancer

(2017) Tiantian Lu et al.   Oncotarget

TGF-β: the connecting link between nephropathy and fibrosis

(2016) Brijesh Sutariya et al.   IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY

Xerostomia of Various Etiologies: A Review of the Literature

(2016) Marta Tanasiewicz et al.   Advances in Clinical and Experimental Medicine

WISP1 mediates IL-6-dependent proliferation in primary human lung fibroblasts

(2016) S. Klee et al.   Scientific Reports

Adamts18deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development

(2016) Dalya Ataca et al.   Biology Open

The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin motifs) family

(2015) Richard Kelwick et al.   GENOME BIOLOGY

Blockade of IL-6TransSignaling Attenuates Pulmonary Fibrosis

(2014) Thanh-Thuy T. Le et al.   JOURNAL OF IMMUNOLOGY

Cryptorchidism and Infertility in Rats with Targeted Disruption of the Adamts16 Locus

(2014) Shakila Abdul-Majeed et al.   PLoS One

The Syndrome of Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus (MMCAT) Is Caused by Mutations inADAMTS18

(2013) Mohammed A. Aldahmesh et al.   HUMAN MUTATION

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

(2013) Ivana Peluso et al.   Orphanet Journal of Rare Diseases

The laminin family

(2013) Monique Aumailley   Cell Adhesion & Migration

Regulation of interleukin-33 and thymic stromal lymphopoietin in human nasal fibroblasts by proinflammatory cytokines

(2012) Kazuaki Nomura et al.   LARYNGOSCOPE

A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity

(2012) Lorna M. Lopez et al.   NEUROBIOLOGY OF AGING

Targeted disruption of Adamts16 gene in a rat genetic model of hypertension

(2012) K. Gopalakrishnan et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Identification of ADAMTS18 as a gene mutated in Knobloch syndrome

(2011) M. A. Aldahmesh et al.   JOURNAL OF MEDICAL GENETICS

Interleukin-33 expression is specifically enhanced in inflamed mucosa of ulcerative colitis

(2010) Ayako Kobori et al.   JOURNAL OF GASTROENTEROLOGY

Genome-wide Association and Follow-Up Replication Studies Identified ADAMTS18 and TGFBR3 as Bone Mass Candidate Genes in Different Ethnic Groups

(2009) Dong-Hai Xiong et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Identification of a mechanochemical checkpoint and negative feedback loop regulating branching morphogenesis

(2009) William P. Daley et al.   DEVELOPMENTAL BIOLOGY

A Disintegrin-like and Metalloprotease (Reprolysin-type) with Thrombospondin Type 1 Motif (ADAMTS) Superfamily: Functions and Mechanisms

(2009) Suneel S. Apte   JOURNAL OF BIOLOGICAL CHEMISTRY