Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome

MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes

(2010) Asli Sirmaci et al.   AMERICAN JOURNAL OF HUMAN GENETICS

An agarose spot assay for chemotactic invasion

(2010) Helen Wiggins et al.   BIOTECHNIQUES

Collective Chemotaxis Requires Contact-Dependent Cell Polarity

(2010) Eric Theveneau et al.   DEVELOPMENTAL CELL

A Novel Mannose-binding Lectin/Ficolin-associated Protein Is Highly Expressed in Heart and Skeletal Muscle Tissues and Inhibits Complement Activation

(2010) Mikkel-Ole Skjoedt et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Collectin 11 (CL-11, CL-K1) Is a MASP-1/3-Associated Plasma Collectin with Microbial-Binding Activity

(2010) S. Hansen et al.   JOURNAL OF IMMUNOLOGY

Basal body stability and ciliogenesis requires the conserved component Poc1

(2009) Chad G. Pearson et al.   JOURNAL OF CELL BIOLOGY

MAp44, a Human Protein Associated with Pattern Recognition Molecules of the Complement System and Regulating the Lectin Pathway of Complement Activation

(2009) S. E. Degn et al.   JOURNAL OF IMMUNOLOGY

Blepharophimosis, blepharoptosis, defects of the anterior chamber of the eye, caudal appendage, radioulnar synostosis, hearing loss and umbilical anomalies in sibs: 3MC syndrome?

(2008) Gabriela F. Leal et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The receptor tyrosine kinase RET regulates hindgut colonization by sacral neural crest cells

(2007) Jean-Marie Delalande et al.   DEVELOPMENTAL BIOLOGY