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Synthesis and structure of copper (II) complexes with L–OH (L–OH = 2,6-bis-[N-(2-pyridylethyl)-formidoyl]-4-methyl-phenol)
(2007)
The synthesis and molecular structures of three new copper (II) complexes with the ligand 2,6-bis-[N-(2-pyridylethyl)-formidoyl]-4-methyl phenol (L-OH) are reported. The complexes were prepared by reaction of L-OH with ...
Loss of heterozygosity in the short arm of human chromosome 3 in sporadic lung cancer.
(2011-11-11)
Introduction: Loss of Heterozygocity (LOH) in the short arm of human chromosome 3 (3p) is a frequent event in different
types of sporadic tumors, including lung cancer (LC).
Aim: To determine 3p LOH in LC samples using ...
EditorialEditorial
(Sociedade Brasileira de Química, 2009)
Método po shen loh y aprendizaje de ecuaciones cuadráticas en estudiantes de secundaria de instituciones educativas de Lamas, 2022
(Universidad Católica de Trujillo "Benedicto XVI" - Fondo EditorialPE, 2023)
El presente trabajo de investigación tuvo como propósito determinar la relación que existe
entre el método Po-Shen Loh y el aprendizaje de ecuaciones cuadráticas en estudiantes de
secundaria de instituciones educativas ...
Síntesis y Caracterización de Complejos Metálicos Polinucleares Utilizando Cefepima como Ligando Puente
(Universidad de Oriente Núcleo de Sucre, 2012)
Loss of heterozygosity of the APC gene in oral squamous cell carcinoma
(ELSEVIER GMBH, URBAN & FISCHER VERLAG, 2008)
The aim of this study was to investigate loss of heterozygosity (LOH) of the APC tumor suppressor gene loci, using restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR) in 40 cases of oral squamous ...
Absence of PRKAR1A loss of heterozygosity in laser-captured microdissected pigmented nodular adrenocortical tissue from a patient with Carney complex caused by the novel nonsense mutation p.Y21X
(Sociedade Brasileira de Endocrinologia e Metabologia, 2008)
OBJECTIVE: Primary pigmented nodular adrenocortical disease (PPNAD) is the main endocrine manifestation of Carney complex, a multiple neoplasia syndrome caused by PRKAR1A gene mutations. The presence of PRKAR1A loss of ...
Investigação da perda de heterozigozidade em 9p, 9q e 17p e de mutações somáticas do TP53 em queilite actínica e carcinoma de células escamosas de lábio
(Universidade Federal de Minas GeraisUFMG, 2015-06-15)
Objectives: Lip squamous cell carcinoma (LSCC) and actinic cheilitis (AC) molecular pathogenesis is unclear. We aimed to assess loss of heterozygostity (LOH) and TP53 mutations in these lesions. Materials and Methods: ...