Roles of the NFI/CTF gene family in transcription and development

RM Gronostajski - Gene, 2000 - Elsevier
The N uclear F actor I (NFI) family of site-specific DNA-binding proteins (also known as CTF
or C AAT box t ranscription f actor) functions both in viral DNA replication and in the …

The matrilins: a novel family of oligomeric extracellular matrix proteins

F Deák, R Wagener, I Kiss, M Paulsson - Matrix Biology, 1999 - Elsevier
The matrilin family at present has four members that all share a structure made up of von
Willebrand factor A domains, epidermal growth factor-like domains and a coiled coil α …

The matrilins: modulators of extracellular matrix assembly

AR Klatt, AKA Becker, CD Neacsu, M Paulsson… - The international journal …, 2011 - Elsevier
The matrilins form a family of oligomeric extracellular adaptor proteins that are most strongly
expressed in cartilage but also present in many other extracellular matrices. Matrilins bind to …

Nuclear factor IX deficiency causes brain malformation and severe skeletal defects

K Driller, A Pagenstecher, M Uhl, H Omran… - … and cellular biology, 2007 - Taylor & Francis
The transcription factor family of nuclear factor I (NFI) proteins is encoded by four closely
related genes: Nfia, Nfib, Nfic, and Nfix. A potential role for NFI proteins in regulating …

Nfix regulates temporal progression of muscle regeneration through modulation of myostatin expression

G Rossi, S Antonini, C Bonfanti, S Monteverde… - Cell reports, 2016 - cell.com
Nfix belongs to a family of four highly conserved proteins that act as transcriptional activators
and/or repressors of cellular and viral genes. We previously showed a pivotal role for Nfix in …

Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration

G Rossi, C Bonfanti, S Antonini, M Bastoni… - Nature …, 2017 - nature.com
Muscular dystrophies are severe disorders due to mutations in structural genes, and are
characterized by skeletal muscle wasting, compromised patient mobility, and respiratory …

Genome-wide meta-analysis of sciatica in Finnish population

S Lemmelä, S Solovieva, R Shiri, C Benner… - PLoS …, 2016 - journals.plos.org
Sciatica or the sciatic syndrome is a common and often disabling low back disorder in the
working-age population. It has a relatively high heritability but poorly understood molecular …

Differential interactions of specific nuclear factor I isoforms with the glucocorticoid receptor and STAT5 in the cooperative regulation of WAP gene transcription

SS Mukhopadhyay, SL Wyszomierski… - … and cellular biology, 2001 - Taylor & Francis
The distal region (− 830 to− 720 bp) of the rat whey acidic protein (WAP) gene contains a
composite response element (CoRE), which has been demonstrated previously to confer …

NF-1C, Sp1, and Sp3 are essential for transcription of the human gene for P450c17 (steroid 17α-hydroxylase/17, 20 lyase) in human adrenal NCI-H295A cells

CJ Lin, JWM Martens, WL Miller - Molecular Endocrinology, 2001 - academic.oup.com
Cytochrome P450c17 catalyzes steroid 17α-hydroxylase and 17, 20 lyase activities, which
are required for the biosynthesis of cortisol and sex steroids. Human P450c17 is expressed …

Characterization of an osteoblast-specific enhancer element in the CBFA1 gene

A Zambotti, H Makhluf, J Shen, P Ducy - Journal of Biological Chemistry, 2002 - ASBMB
Cbfa1 is a critical regulator of cell differentiation expressed only in the osteochondrogenic
lineage. To define the molecular basis of this cell-specific expression we analyzed the …