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Myotonic dystrophy type 1 (DM1) clinical subtypes and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent
(2021)
Myotonic dystrophy type 1 (DM1) is a complex disease with a wide spectrum of symptoms. The exact relationship between
mutant CTG repeat expansion size and clinical outcome remains unclear. DM1 congenital patients (CDM) ...
Induced mutations in crop plants at Instituto de Genética "Ewald A. Favret": mutants of scientific and/or agronomic interest: Induced mutations in crop plants at Instituto de Genética "Ewald A. Favret"
(USFQ PRESS, departamento editorial de la Universidad San Francisco de Quito USFQ, 2021)
Frequency of the MDR1 mutant allele associated with multidrug sensitivity in dogs from Brazil
(2015)
To date, a 4-bp deletion in the MDR1 gene has been detected in more than ten dog breeds, as well as in mixed breed dogs, in several countries, however information regarding this mutation in dogs from Brazil is lacking. For ...
Teste de alelismo entre os mutantes de amadurecimento alcobaça e non-ripening em tomateiroAllelism test between the alcobaça and non-ripening mutants in tomato plants
(Editora da Universidade Federal de Lavras, 2010)
Parasexuality in asexual development mutants of Aspergillus nidulans
(Sociedad de Biología de Chile, 2006)
Mutantes letais termossensíveis em Aspergillus nidulans
(Fundação Oswaldo Cruz. Instituto Oswaldo Cruz., 2020)
Frequencies of-308G/A (TNFA) and-509C/T (TGFB1) polymorphisms in sickle cell anemia patients from Brazil
(Funpec-editora, 2013-01-01)
Sickle cell anemia is an affection that causes chronic inflammation, with consequences for vaso-occlusion, oxidative stress and cytokine production. Genetic polymorphisms in markers involved in this process can modulate ...
Alelo doble mutante en el gen EXT1 no informado previamente en una adolescente con exostosis múltiple hereditariaDouble mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses
(Sociedad Argentina de Pediatría, 2015-04)
Las formas hereditarias de exostosis múltiple, actualmente denominada EXT1/EXT2-CDG dentro de los desórdenes congénitos de la glicosilación, son los tumores óseos benignos más comunes y se caracterizan por la formación de ...