Results 131 to 140 of about 5,848 (206)

Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.

, 2020
Developmental defects affecting the heart and aortic arch arteries are a significant phenotype observed in 22q11 deletion syndrome patients and are caused by a microdeletion on chromosome 22q11. TBX1, one of the deleted genes, is expressed throughout the
Wasay Mohiuddin Shaikh Qureshi (4543342), René Maehr (52396), Helen M Phillips (8114078), Jürgen E Schneider (8281905), Rebecca Dodds (8281896), Simon D Bamforth (8114075), Ramada R Khasawneh (8281887), Kerstin Seidel (385253), Silvia Mazzotta (8281893), Catherine A Stothard (8281878), Ralf Kist (641672), Anastasia I Kousa (8281881), Timothy J Mohun (8274570), Heiko Peters (73270), J Alberto Briones-Leon (8281884), Timothy Bates (8281899), Simon J Cockell (8281902), Rachel Sanders (3739498), Mitsushiro Nakatomi (3180675), Chloe O'Loughlin (8281890)   +19 more
core  

TBX1 wt Allele [PDF]

, 2020
openaire   +1 more source

The role of putative Tbx1 traget genes in the pathogenesis of the 22q11 Deletion Syndrome phenotype.

, 2013
The 22q11 deletion syndrome(22q11DS/DiGeorge Syndrome [DGS]) is a congenital disorder with complex aetiology including cardiovascular, thymic/parathyroid, craniofacial and neuro-behavioural phenotypes.
Roberts, C
core  

T-Box Transcription Factor TBX1 [PDF]

, 2020
openaire   +1 more source

Investigation of the role of Tbx1, an essential T -box gene, in the mesoderm during embryogenesis

, 2008
In vertebrates, the inner ear is comprised of the cochlea and vestibular system, which develop from the otic vesicle. This process is regulated via inductive interactions from surrounding tissues.
Braunstein, Evan Mark
core  

Understanding normal cardiac morphogenesis and its disruptions: a journey through pathways. [PDF]

Front Genet
Saliba AL, Afiune J, Pic-Taylor A, Oliveira SF, Mazzeu JF.   +4 more
europepmc   +1 more source

3D chromatin organisation contributes to the regulatory logic in differentiating lymphatic endothelium. [PDF]

EMBO Rep
Panara V, Arnold H, Gloger M, Skoczylas R, Vidal Gutierrez V, Johansson A, Smialowska A, Koltowska K.   +7 more
europepmc   +1 more source

Tetralogy of Fallot: Genetic, Epigenetic and Clinical Insights into a Multifactorial Congenital Heart Disease. [PDF]

Genes (Basel)
Gagliardi MF, Micaglio E, Micheletti A, Benedetti S, Negura DG, Bevilacqua F, Guglielmi G, Pasqualin G, Giamberti A, Chessa M.   +9 more
europepmc   +1 more source

Aberrant expression of MAPK1 and MCTS1 in chronic myeloid leukemia (CML). [PDF]

MicroPubl Biol
Kortendick L, Meyer C, Nagel S.
europepmc   +1 more source

Elucidation of the XX/XY Sex Determination System and Development of a Sex-Linked Molecular Marker in the Freshwater Snail <i>Bellamya purificata</i>. [PDF]

Animals (Basel)
Gao Y, Wen Y, Yi S, Lin Y, Peng J, Pan X, Zhou X.   +6 more
europepmc   +1 more source