Search Results - "Gimelli G"

Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk.

Authors: Carlson, Jenna C. Zhang, Xinyi Erdogan-Yildirim, Zeynep et al.

Source: PLoS Genetics. 9/30/2025, Vol. 21 Issue 9, p1-21. 21p.

Comparison of the patency rates of catheter placement via the right external jugular vein route versus the right brachiocephalic vein route in patients experiencing tunneled-cuffed catheter loss.

Authors: Yin, Jun Wang, Fengping

Source: Renal Failure. Dec2025, Vol. 47 Issue 1, p1-8. 8p.

Decitabine-mediated DNA methylation dynamics at pericentromeric satellite 2 repeats.

Authors: Sordini, Enrica Ciurlia, Eugenia Zanella, Alessia et al.

Source: BMC Cancer. 11/18/2025, Vol. 25 Issue 1, p1-11. 11p.

Ganglioside Profiling Uncovers Distinct Patterns in High-Risk Neuroblastoma.

Authors: Paret, Claudia Wingerter, Arthur Seidmann, Larissa et al.

Source: International Journal of Molecular Sciences. Sep2025, Vol. 26 Issue 17, p8431. 21p.

Delayed intervention in a giant coronary bypass saphenous graft aneurysm: a case report.

Authors: Passos, Mariana Gerardo, Filipa Loureiro, José et al.

Source: World Journal of Emergency Medicine. Nov2025, Vol. 16 Issue 6, p626-628. 3p.

Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome identified by whole-exome sequencing (WES): a case report from a developing country.

Authors: Joma, Rahaf Radwan, Shahed Hannoun, Sakhaa et al.

Source: Oxford Medical Case Reports. Jun2025, Vol. 2025 Issue 6, p1-3. 3p.

Thrombosed saphenous vein graft aneurysm mimicking left atrial appendage mass: A rare complication of coronary artery bypass graft.

Authors: Shahab, Hunaina Kassem, Jad Yildiz, Ali et al.

Source: Journal of Clinical Imaging Science. Jul2025, Vol. 15, p1-4. 4p.

Is there a predisposition to uveitis in Turner syndrome?

Authors: Stephenson, Kirk A. J. Dhanji, Shanil R. Pakzad-Vaezi, Kaivon

Source: Ophthalmic Genetics. Jun2025, Vol. 46 Issue 3, p297-300. 4p.

Placental mosaicism in prenatal diagnosis.

Authors: Döttelmayer MSc., Patricia Fauth, Christine

Source: Medizinische Genetik. Apr2026, Vol. 38 Issue 2, p139-149. 11p.

Pigmentary anomaly caused by mosaic 3q22.2q29 duplication.

Authors: Martinez‐Falero, Beatriz Suarez Koutalopoulou, Anastasia Douglas, Andrew G. L. et al.

Source: Clinical & Experimental Dermatology. Dec2022, Vol. 47 Issue 12, p2342-2345. 4p. 2 Color Photographs.

Anaesthesia in a Child With 9q13-q21 Deletion Syndrome: Tailored Perioperative Management in a Rare Genetic Disorder.

Authors: HARSHITHA, C. PATIL, CHAITALI SHASHIKANT BAKHSHI, ROCHANA GIRISH

Source: Journal of Clinical & Diagnostic Research. May2026, Vol. 20 Issue 5, p1-3. 3p.

Nucleocapsid Protein of SARS-CoV-2 Upregulates RANTES Expression in A172 Glioblastoma Cells.

Authors: Gadilgereyeva, Bakhytgul Kunushpayeva, Zhanar Abdrakhmanova, Mira et al.

Source: Molecules. Mar2025, Vol. 30 Issue 5, p1066-1. 15p.

Residual risk of clinically significant copy number variations in fetuses with ultrasonographic soft markers following exclusion of non-invasive prenatal screening-detectable findings.

Authors: Liang Y Zhou R Liu T et al.

Source: Archives of gynecology and obstetrics [Arch Gynecol Obstet] 2026 Mar 18; Vol. 313 (1). Date of Electronic Publication: 2026 Mar 18.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 8710213 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-0711 (Electronic) Linking ISSN: 09320067 NLM ISO Abbreviation: Arch Gynecol Obstet Subsets: MEDLINE

Phosphorylation of Xenopus M18BP1 governs centromeric localization and CENP-A nucleosome assembly.

Authors: Brown RR Schwartz JP Ghadri L et al.

Source: EMBO reports [EMBO Rep] 2026 Mar; Vol. 27 (6), pp. 1561-1579. Date of Electronic Publication: 2026 Feb 12.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 100963049 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1469-3178 (Electronic) Linking ISSN: 1469221X NLM ISO Abbreviation: EMBO Rep Subsets: MEDLINE

Partial detachment of the aorta: a fatal complication of CPR chest compressions.

Authors: Szemień, Michał Burchardt, Bartosz Dolińska-Kaczmarek, Klaudia et al.

Source: Bulletin of the National Research Centre. 4/24/2023, Vol. 47 Issue 1, p1-4. 4p.

Shared Disease Mechanisms in Neurodevelopmental Disorders: A Cellular and Molecular Biology Perspective.

Authors: Pattie, Elizabeth A. Iffland II, Philip H.

Source: Brain Sciences (2076-3425). Jan2026, Vol. 16 Issue 1, p54. 35p.

A 250-kb Microdeletion Identified in Chromosome 16 Is Associated With Non-Syndromic Sensorineural Hearing Loss in a South Indian Consanguineous Family.

Authors: Swetha, Jayakumar Sakthignanavel, Arulmozhi Manoharan, Aarthi et al.

Source: Journal of Audiology & Otology. Jan2025, Vol. 19 Issue 1, p31-37. 7p.

Right ventricular dysfunction and impaired right ventricular–pulmonary arterial coupling in paradoxical low‐flow, low‐gradient aortic stenosis.

Authors: Nies, Richard J. Nettersheim, Felix S. Braumann, Simon et al.

Source: European Journal of Heart Failure. Nov2024, Vol. 26 Issue 11, p2340-2352. 13p.

Rare within Rare: A Girl with Severe Haemophilia A and Turner Syndrome.

Authors: Blag, Cristina Serban, Margit Ursu, Cristina Emilia et al.

Source: Journal of Clinical Medicine. Dec2023, Vol. 12 Issue 23, p7437. 9p.

A Rare Case of Mosaic 3pter and 5pter Deletion-Duplication with Autism Spectrum Disorder and Dyskinesia.

Authors: Bajracharya, Luna Lall, Meena Bijarnia-Mahay, Sunita et al.

Source: Case Reports in Genetics. 10/16/2023, p1-9. 9p.