Results 241 to 250 of about 105,581 (338)

Management of the Difficult Paediatric Airway with a Simple Fiberoptic-Assisted Laryngoscope: A Report of Two Cases with Pierre Robin and Patau's (Trisomy 13) Syndrome

, 2014
Alper Kılıçaslan, Ayşe Erol, Ahmet Topal, Tayfun Et, Şeref Otelcioğlu   +4 more
openalex   +2 more sources

Preventing Differentiation Towards Primitive Macrophages in Stem Cells With Down Syndrome

Immunology, Volume 177, Issue 3, Page 596-612, March 2026.
Decreased fetal brain macrophages were previously reported in Ts1Cje mice, a model of Down syndrome (DS). We confirmed the reduction in primitive macrophages, brain macrophage precursors, using Ts1Cje‐derived mouse embryonic stem cells (Ts1Cje‐mESCs) and human induced pluripotent stem cells with trisomy 21 (Tri21‐hiPSCs), with in vivo validation ...
Koki Harada, Keiichi Ishihara, Sayaka Wakayama, Teruhiko Wakayama, Sae Yamamoto, Haruhiko Sago, Shun Shimohama, Satoshi Akiba, Florent Ginhoux, Kazuyuki Takata   +9 more
wiley   +1 more source

Abernethy Malformation Type Ib in a Patient With Trisomy 21: A Rare Case of Portal Vein Absence, Mesenteric Thrombosis, and Bowel Perforation. [PDF]

Cureus
Benignus C, Müller-Kühnle J, Popescu M, Goeppert B, Schiedeck T.   +4 more
europepmc   +1 more source

Shape and Morphology of the Sella Turcica in Patients with Trisomy 21-A Systematic Review. [PDF]

Diagnostics (Basel)
Mazuś M, Szemraj-Folmer A, Stasiak M, Studniarek M.   +3 more
europepmc   +1 more source

The value of quantitative fluorescence polymerase chain reaction for the products of conception in the era of copy number variation sequencing. [PDF]

Front Genet
Yang S, Zhang H, Wang Y, Zhang Q, Wu Y, Fu X, Li R.   +6 more
europepmc   +1 more source

Anaysis of the association between chromosomal abnormalities in early missed abortion embryos and maternal age and AMH levels based on CNV-Seq. [PDF]

BMC Pregnancy Childbirth
Huang S, Huang T, Liu D, Yuan H, Zhou Y, Zeng B, Bai G.   +6 more
europepmc   +1 more source

Maternal mixed UPD3 and a homozygous PLXNA1 c.2497G>C variant in a fetus with severe anomalies. [PDF]

Front Med (Lausanne)
Ye Y, Wang X, He Y, Ning H, Zhang Z, Tao F, Zou Z, Fang Q, Chen Z, Tian X, Hao X.   +10 more
europepmc   +1 more source

Integrated Genomic and Transcriptomic Profiling of Isolated Trisomies in AML Reveals Cell Cycle Dysregulation and Therapeutic Vulnerabilities. [PDF]

J Cell Mol Med
Maués JHDS, Duarte BKL, Svidnicki MCCM, Filho HLAS, Niemann FS, Duarte ADSS, de Melo Campos P, Moraes-Vieira PM, Olalla Saad ST.   +8 more
europepmc   +1 more source

Behçet-like Syndromes: A Comprehensive Review. [PDF]

Dermatopathology (Basel)
Mancuso G, Salvadè I, Ogna A, Balestra B, Beltraminelli H.   +4 more
europepmc   +1 more source

Low-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, positive non-invasive prenatal testing for trisomy 14, perinatal progressive decrease of the trisomy 14 cell line and a favorable fetal outcome

Chih‐Ping Chen, Fang-Tzu Wu, Sui‐Yuan Chang, Peih-Shan Wu, Yen-Ting Pan, Meng‐Shan Lee, Chien-Ling Chiu, Wayseen Wang   +7 more
openalex   +1 more source