P. Thomas

J. Aubin, R. Franceschi, P. Thomas, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

A Homeodomain Protein Binding Element in the Bone Sialoprotein Promoter is Critical for Tissue-Specific Expression in Bone

R. Franceschi, P. Thomas, R. Gopalakrishnan, 2003, Connective tissue research.

Molecular cloning of cDNAs encoding human GLEPP1, a membrane protein tyrosine phosphatase: characterization of the GLEPP1 protein distribution in human kidney and assignment of the GLEPP1 gene to human chromosome 12p12-p13.

R. Wiggins, J. Wiggins, P. Thomas, 1995, Genomics.

Activation of the Pro-survival Phosphatidylinositol 3-Kinase/AKT Pathway by Transforming Growth Factor-β1 in Mesenchymal Cells Is Mediated by p38 MAPK-dependent Induction of an Autocrine Growth Factor*

V. Keshamouni, J. Horowitz, V. Thannickal, 2004, Journal of Biological Chemistry.

MAPK Pathways Activate and Phosphorylate the Osteoblast-specific Transcription Factor, Cbfa1*

G. Karsenty, K. Guan, R. Franceschi, 2000, The Journal of Biological Chemistry.

Novel multilocus imprinting disturbances in a child with expressive language delay and intellectual disability

M. Hannibal, J. Bedoyan, J. Innis, 2022, American journal of medical genetics. Part A.

Myofibroblast Differentiation by Transforming Growth Factor-β1 Is Dependent on Cell Adhesion and Integrin Signaling via Focal Adhesion Kinase*

R. Day, E. White, J. Horowitz, 2003, Journal of Biological Chemistry.

PGE(2) inhibition of TGF-beta1-induced myofibroblast differentiation is Smad-independent but involves cell shape and adhesion-dependent signaling.

E. White, M. Peters-Golden, V. Thannickal, 2007, American journal of physiology. Lung cellular and molecular physiology.

Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.

M. Russell, J. Bernat, J. Innis, 2014, Human molecular genetics.

Differential impact of a dyskeratosis congenita mutation in TPP1 on mouse hematopoiesis and germline

C. Keegan, I. Maillard, J. Nandakumar, 2021, Life Science Alliance.

High-throughput gene expression analysis identifies p53-dependent and -independent pathways contributing to the adrenocortical dysplasia (acd) phenotype.

Ceren Sucularlı, C. Keegan, H. Koçak, 2018, Gene.

Analysis of De Novo HOXA13 Polyalanine Expansions Supports Replication Slippage Without Repair in Their Generation

C. Keegan, K. Owens, D. Roulston, 2013, American journal of medical genetics. Part A.

Molecular Cloning, Expression, and Characterization of Podocalyxin-like Protein 1 from Rabbit as a Transmembrane Protein of Glomerular Podocytes and Vascular Endothelium *

R. Wiggins, C. Whiteside, D. Kershaw, 1995, The Journal of Biological Chemistry.

Molecular Cloning and Characterization of Human Podocalyxin-like Protein

R. Wiggins, D. Kershaw, J. Wiggins, 1997, The Journal of Biological Chemistry.

A Novel Intergenic ETnII-β Insertion Mutation Causes Multiple Malformations in Polypodia Mice

J. Nadeau, J. Lehoczky, A. Borowsky, 2013, PLoS genetics.

Identification of a Homeodomain Binding Element in the Bone Sialoprotein Gene Promoter That Is Required for Its Osteoblast-selective Expression*

R. Franceschi, P. Thomas, M. Benson, 2000, The Journal of Biological Chemistry.

Cysteinyl Leukotrienes Are Autocrine and Paracrine Regulators of Fibrocyte Function1

M. Peters-Golden, B. Moore, G. Toews, 2007, The Journal of Immunology.

Analysis of De Novo HOXA13 Polyalanine Expansions Supports Replication Slippage Without Repair in Their Generation

C. Keegan, K. Owens, D. Roulston, 2013, American journal of medical genetics. Part A.

A Role for IL-1 Receptor-Associated Kinase-M in Prostaglandin E2-Induced Immunosuppression Post-Bone Marrow Transplantation

T. Standiford, R. Flavell, M. Ballinger, 2010, The Journal of Immunology.