Results 111 to 120 of about 3,069 (190)

Paired-Box (PAX) Gene Signatures as a Biomarker of Breast Cancer Progression. [PDF]

Int J Mol Sci
Scimeca M, Scioli MP, Palumbo V, Funke L, Woodsmith J, Servadei F, Giacobbi E, Seghetti C, Buonomo OC, Candi E, Treglia M, Marsella LT, Melino G, Mauriello A, Bonfiglio R.   +14 more
europepmc   +1 more source

Epigenetic, Genetic, and Functional Germline Alterations of <i>PAX</i> Genes in Human Pathology: A Comprehensive Update. [PDF]

Curr Issues Mol Biol
Gomez VL, Wegner S, Ocejo S, Perez D, Jabbour D, Fernandez V, Abulaban A, Bahmad M, Elajami TK, Abou-Kheir W, Bahmad HF.   +10 more
europepmc   +1 more source

Whole exome sequencing and cluster analysis reveal that EPB41L4A mutation may trigger tooth agenesis. [PDF]

PLoS One
Li TQ, Zhang Q, Wang HJ, Ma ZF, Lu BY, Hou KG, Zhang XY.   +6 more
europepmc   +1 more source

Next-Generation Sequencing Data and Clinical Features in Patients with Cleft Palate and Tooth Agenesis: A Systematic Literature Review. [PDF]

Dent J (Basel)
Boutahari N, Belayachi L, Ghoul S.
europepmc   +1 more source

Toward Understanding the Role of miRNAs in Cleft Palate Only: Observations from Patient Tissues and In Vitro Assays. [PDF]

Int J Mol Sci
Palmieri A, Scapoli L, Pellati A, Apolloni F, Zanchi V, Spinelli G, Sgarzani R, Carinci F, Martinelli M.   +8 more
europepmc   +1 more source

Single cell spatial transcriptomics links Wnt signaling disruption to extracellular matrix development in a cleft palate model. [PDF]

Sci Rep
Piña JO, Raju R, Stipano E, Myo AC, Wang Z, Ono M, Chattaraj P, Furukawa M, D'Souza RN.   +8 more
europepmc   +1 more source

Dissecting the Genetic Contribution of Tooth Agenesis. [PDF]

Int J Mol Sci
Fallea A, Vinci M, L'Episcopo S, Bartolone M, Musumeci A, Ragalmuto A, Treccarichi S, Calì F.   +7 more
europepmc   +1 more source

Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia

Missing teeth (hypodontia and oligodontia) are a common developmental abnormality in humans and heterozygous mutations of PAX9 have recently been shown to underlie a number of familial, non-syndromic cases.
Peters H, Reid DJ, Kist R, Watson M, Wang X, Cairns P, Miles C   +6 more
core  

The Ecto-Endodermal Boundary in the Oral and Pharyngeal Mucosa: A Narrative Review. [PDF]

Life (Basel)
Schipperheijn R, Dikkers FG, de Bakker BS.   +2 more
europepmc   +1 more source

Diverging pathomechanisms underlying collagen I-related and MBTPS2-related osteogenesis imperfecta: insights from patient-derived fibroblasts and iPSC-based modelling of bone. [PDF]

Front Endocrinol (Lausanne)
Lim PJ, Marcionelli G, Blättler C, Gut S, Rohrbach M, Giunta C.   +5 more
europepmc   +1 more source