Results 21 to 30 of about 138,218 (248)
Cor triatriatum sinister with situs inversus totalis in an infant. [PDF]
Cor triatriatum sinister is a rare congenital cardiac malformation characterized by a membrane in the left atrium which separates the left atrium into the proximal and distal chambers.Association of cor triatriatum is extremely rare with situs inversus
Taksande, Amar M. +3 more
core
Finding novel vulnerabilities of hypomorphic BRCA1 alleles
Synthetic lethality screens performed to identify novel vulnerabilities often model complete gene loss, thereby overlooking patient‐derived hypomorphic mutations. In this study, we have performed genome‐wide CRISPR screens on BRCA1 hypomorphic mutations, showing BRCA1I26A behaves like wild‐type, while BRCA1R1699Q mimics deficiency. Furthermore, we have
Anne Schreuder +10 more
wiley +1 more source
Avaliação visual da cor dental mediante diferentes iluminantes [PDF]
TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Odontologia.Objetivo: avaliar a percepção visual da cor de estudantes de Odontologia mediante o uso de diferentes iluminantes: luzes natural, incandescente e ...
Bahr, Manuela da Luz Fontes
core
MITF maintains genome stability in nonmelanocyte lineages
MITF is essential for melanocyte survival and acts as an oncogene in 10%–20% of melanomas. We show that MITF depletion causes genome instability in nonmelanocytic cells, leading to LATS2‐mediated P53 activation, cell cycle arrest, and apoptosis. This study highlights the role of MITF as a genome maintenance factor beyond the melanocyte lineage. Created
Drifa H. Gudmundsdottir +13 more
wiley +1 more source
Funktionelle Charakterisierung der C-terminalen-Domänen des Korepressors N-CoR [PDF]
Although in general cells are genetically identical in multicellular organisms, the differential expression of genomic information enables cell type definition and specific organ function.
Ducasse, Miryam
core
Isocitrate dehydrogenase 1 (IDH1) mutations are highly recurrent in multiple human cancer types, including cholangiocarcinoma and glioma. IDH1 R132C is the most common IDH1 mutation in cholangiocarcinoma and likely arises from APOBEC3A‐ or APOBEC3B‐mediated deamination.
Kelly E. Butler +3 more
wiley +1 more source
ABSTRACT Background Collaterals are crucial factors that influence the infarct growth rate (IGR). We aimed to determine whether a comprehensive multimodal collateral score (MCS), incorporating collateral assessment at the arterial, tissue, and venous levels, is associated with functional independence and provides incremental prognostic value over ...
Giorgio Busto +12 more
wiley +1 more source
Resumen: Introducción: La demencia por cuerpos de Lewy es una entidad neurológica de carácter degenerativo y progresivo que puede asociar clínica heterogénea: demencia, psicosis, alteraciones de la sensopercepción y de conducta, parkinsonismo, etc ...
Jaume Clemente Calvo +3 more
doaj +1 more source
Objective This study aimed to investigate hand function trajectories over five years in primary hand osteoarthritis (OA). Additionally, determinants of baseline and longitudinal hand function were assessed. Methods A total of 538 patients with both baseline and five‐year study visits were analyzed.
Annemiek V. E. M. Olde Meule +4 more
wiley +1 more source
Loculated empyema in a neonate successfully treated with chest tube thoracostomy and antibiotics
Empyema thoracis, defined as the accumulation of pus in the pleural space, is a rare entity in the neonatal period. There are very few cases described in the medical literature and there are still no treatment protocols in the management of empyema in ...
John Robyn V. Diez +3 more
doaj +1 more source

