D. Napierala

发表

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.

Brendan H. Lee, Q. Zheng, Guang Zhou, 2005, Molecular genetics and metabolism.

Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues

B. Dawson, O. Lichtarge, Brendan H. Lee, 2014, PLoS genetics.

Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome.

R. Shivdasani, Brendan H. Lee, Q. Zheng, 2008, Human molecular genetics.

Mosaicism in tuberous sclerosis as a potential cause of the failure of molecular diagnosis.

D. Kwiatkowski, J. Kwiatkowska, R. Słomski, 1999, The New England journal of medicine.

Transcriptional Repression of the Dspp Gene Leads to Dentinogenesis Imperfecta Phenotype in Col1a1-Trps1 Transgenic Mice

B. Dawson, Brendan H. Lee, R. D'Souza, 2012, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Reactive oxygen species (ROS) generation as an underlying mechanism of inorganic phosphate (Pi)-induced mineralization of osteogenic cells.

S. Khalid, E. Beniash, D. Napierala, 2020, Free radical biology & medicine.

Molecular Diagnostics of Genetic Diseases: Experience from Studies of DMD, APC, TSC1, and OPG Genes. Part 1.

R. Słomski, A. Pławski, J. Jura, 2000 .

Mutations in SERPINF1 Cause Osteogenesis Imperfecta Type VI

B. Dawson, R. Gibbs, F. Glorieux, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Crane‐Heise syndrome: A second familial case report with elaboration of phenotype

E. Zackai, L. Medne, Brendan H. Lee, 2003, American journal of medical genetics. Part A.

Deficiency of Mineralization-Regulating Transcription Factor Trps1 Compromises Quality of Dental Tissues and Increases Susceptibility to Dental Caries

C. Roberts, E. Beniash, D. Napierala, 2022, Frontiers in Dental Medicine.

Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome

P. Beighton, Y. Gillerot, N. Elçioglu, 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Trps1 transcription factor represses phosphate-induced expression of SerpinB2 in osteogenic cells.

S. Khalid, E. Beniash, D. Napierala, 2020, Bone.

Extracellular vesicles present in bone, blood and extracellular matrix have distinctive characteristics and biologic roles

S. Badylak, S. Mullett, S. Wendell, 2022, Journal of Immunology and Regenerative Medicine.

Dual Role of the Trps1 Transcription Factor in Dentin Mineralization*

J. Millán, Brendan H. Lee, M. Bottini, 2014, The Journal of Biological Chemistry.

Runx2 contributes to murine Col10a1 gene regulation through direct interaction with its cis-enhancer

Brendan H. Lee, Q. Zheng, Yuqing Chen, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

CONSEQUENCES OF TRPS 1 DEFICIENCY ON DENTINOGENESIS by MORGAN A

Committee Chair, M. MacDougall, D. Napierala, 2015 .

Dspp-independent Effects of Transgenic Trps1 Overexpression on Dentin Formation

C. Qin, P. Jani, D. Napierala, 2015, Journal of dental research.

Proteomic profiling of extracellular vesicles released from vascular smooth muscle cells during initiation of phosphate-induced mineralization

S. Khalid, J. Conway, J. Mobley, 2018, Connective tissue research.

Phosphate induces formation of matrix vesicles during odontoblast-initiated mineralization in vitro.

J. Millán, T. Dokland, E. Beniash, 2016, Matrix biology : journal of the International Society for Matrix Biology.

Specificity protein 7 is not essential for tooth morphogenesis

J. C. Clarke, A. Javed, B. Crombrugghe, 2014, Connective tissue research.

De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia

P. Stankiewicz, J. Mulvihill, Jiyun Lee, 2008, American journal of medical genetics. Part A.

The presence of germ line mosaicism in cleidocranial dysplasia

R. Sutphen, B. Lee, T. Pal, 2007, Clinical genetics.

Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

D. Stockton, Brendan H. Lee, R. Mendoza-Londono, 2005, American journal of human genetics.

Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion

Brendan H. Lee, D. Napierala, Brian Kelley, 2019, Front. Physiol..

Tricho-Rhino-Phalangeal Syndrome with Supernumerary Teeth

R. Shivdasani, V. Praphanphoj, P. T. Sharpe, 2008, Journal of dental research.

Toxic RNA in Pathogenesis of Human Neuromuscular Disorders

M. Napierala, D. Napierala, D. Napierała, 2008 .

Trps1 transcription factor regulates mineralization of dental tissues and proliferation of tooth organ cells.

D. Napierala, K. Verdelis, Mairobys Socorro, 2019, Molecular genetics and metabolism.

Localization of the Cis‐Enhancer Element for Mouse Type X Collagen Expression in Hypertrophic Chondrocytes In Vivo

B. Keller, A. Parker, Brendan H. Lee, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

RUNX2 and Cleidocranial Dysplasia

L. Burrage, Yangjin Bae, D. Napierala, 2016 .

A note on ryanodine receptor gene [ryr 1] occurence in the anserine genome

P. Gronek, R. Słomski, A. Pławski, 1999 .

The Growth and Aggressive Behavior of Human Osteosarcoma Is Regulated by a CaMKII-Controlled Autocrine VEGF Signaling Mechanism

Yang Yang, D. Napierala, Paul G Daft, 2015, PloS one.

Sequence polymorphism of exon 17 of the ryanodine receptor gene [ryr1] in the Canidae

P. Gronek, R. Słomski, A. Pławski, 2000 .