Results 121 to 130 of about 131,496 (305)

1. congreso de la Sociedad EspaNola de Genetica

, 1997
Centro de Informacion y Documentacion Cientifica (CINDOC). C/Joaquin Costa, 22. 28002 Madrid.
Valencia Univ. (Spain). Dept. de Genetica, Sociedad EspaNola de Genetica, Madrid (Spain)   +1 more
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Genomics‐informed management of ex situ populations

Conservation Biology, EarlyView.
Abstract The European Association of Zoos and Aquariums (EAZA) manages insurance populations for hundreds of species through its EAZA ex situ programs (EEPs). EEPs help safeguard against extinction in the wild and provide source populations for genetic rescue programs.
Cock van Oosterhout, Philippe Helsen, Elmar Fienieg, Claudia Fontsere, Linett Rasmussen, Mirte Bosse, Zjef Pereboom, Christina Hvilsom, Hernán E. Morales   +8 more
wiley   +1 more source

Evolución o creación, genomas y clonación [PDF]

Nómadas, 2001
El texto –siguiendo el proceso histórico-científico–, muestra la importancia de los estudios referidos a la creación y evolución, tanto del genoma humano como de la clonación, los temores que se generaron alrededor de los avances propuestos por la ...
Emilio Yunis
doaj  

Refining risk stratification after indeterminate urinary cytology: Evidence from Bladder EpiCheck. [PDF]

Cancer Cytopathol
Abstract Background This study aimed to evaluate Bladder EpiCheck (BE) performance in detecting urothelial carcinoma (UC) and HG (high‐grade) events in patients with indeterminate cytology and negative cystoscopy. Methods This prospective study included 63 patients who presented with indeterminate urinary cytology and negative cystoscopy between ...
Mercader C, Ingelmo-Torres M, Roldán FL, Figueras M, Villalba E, Galve P, Asiaín I, Costa M, Vilaseca A, Oriola J, Franco A, Alcaraz A, Mengual L.   +12 more
europepmc   +2 more sources

Descrição atualizada da paralisia cerebral

Developmental Medicine &Child Neurology, EarlyView.
Resumo A paralisia cerebral (PC) é um termo descritivo amplamente utilizado para um espectro de deficiências motoras causadas por lesão ou malformação cerebral não progressiva ocorrida durante as fases iniciais do desenvolvimento. Avanços recentes nas áreas da genética, de pesquisa em inflamação e em neurofisiologia têm refinado a compreensão ...
Bernard Dan, Peter Rosenbaum, Lucinda Carr, Martin Gough, John Coughlan, Nonyelum Nweke   +5 more
wiley   +1 more source

27. Jornadas de genetica luso-espaNolas

, 1993
Available from Centro de Informacion y Documentacion Cientifica CINDOC. Joaquin Costa, 22. 28002 Madrid.
Extremadura Univ., Caceres (Spain), Sociedad EspaNola de Genetica, Madrid (Spain)   +1 more
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Atividade e participação de crianças e adolescentes com paralisia cerebral: um estudo transversal multicêntrico no Brasil

Developmental Medicine &Child Neurology, EarlyView.
Resumo Objetivo Avaliar os efeitos diretos, indiretos, mediadores e moderadores sobre o desempenho de atividades e a participação de crianças e adolescentes com paralisia cerebral (PC), sob a perspectiva da Classificação Internacional de Funcionalidade, Incapacidade e Saúde (CIF).
Déborah E Fontes, Kênnea M A Ayupe, Paula S C Chagas, Robert J Palisano, Hércules R Leite, Ana Cristina R Camargos   +5 more
wiley   +1 more source

Comparative diagnostic challenges in two horses with skin fragility disorders

Equine Veterinary Education, EarlyView.
Summary Hereditary equine regional dermal asthenia (HERDA) is an autosomal recessive connective tissue disorder of horses caused by a missense mutation (c.115G>A) in the peptidyl‐prolyl cis–trans isomerase B (PPIB) gene, resulting in defective collagen organisation.
M. Biolchi, F. A. Saiki, T. G. Cristo, M. C. Silva, R. J. Souza, A. F. Souza, R. A. Casagrande, J. H. Fonteque, C. I. G. Vogel   +8 more
wiley   +1 more source

CancerHubs Data Explorer: a web application for investigating mutation-enriched protein interaction hubs in human cancers

BioData Mining
Background Cancer gene discovery has traditionally relied on single-gene analyses of genomic or transcriptomic data. However, cancer is now recognized as a complex, systems-level disease driven by the coordinated dysregulation of interconnected gene sets.
Ivan Ferrari, Elisa Arsuffi, Stefano Biffo, Nicola Manfrini   +3 more
doaj   +1 more source

GENETICA GENERALE

, 2020
Genetica formale Metodo e prove sperimentali di Mendel Caratteri singoli e segregazione, Caratteri e assortimento indipendente, Esperienze mendeliane "ieri ed oggi", I Leggi di Mendel, I Caratteri mendeliani e reincrocio IGenetica "oltre ...
FASANO,S, TOGNON,M, BARISANI,D, DE LEO,G, DI BELLA,MA, MENEVERI,R   +5 more
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