Anatomical aspects of the gynoecium of species of Anthurium sect. Urospadix Engl. (Araceae, Alismatales)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Morphology of trichomes in Tibouchina sect. Pleroma (D-Don) Cogn. (Melastomataceae)

The Melastomataceae display greater trichome diversity. Dr. Wurdack, in his Atlas of hairs, recognized 46 types of trichomes for the Neotropical Melastomataceae through the Scanning Electron Microscope (SEM), and referred 17 of them to the genus Tibouchina. The trichome morphology has been extensively used in the delimitation of the taxa in Melastomataceae, as well as in previous studies by Cogniaux, the monograph of Brazilian Melastomataceae published in 1885. The morphology of the trichomes was essential for the delimitation of several species in Tibouchina section Pleroma. The use of SEM provided the best characterization of the 15 different types of trichomes recognized among the 41 species examined. These were described based on the morphological appearance, both optical microscopy and scanning electron microscopy, and illustrated by scanning electron micrographs and photomicrographs.

Morfologia dos tricomas em Tibouchina sect. Pleroma (D. Don) cogn. (melastomataceae)

Melastomataceae é a família que apresenta a maior diversidade de tricomas. Dr. Wurdack em seu Atlas of hairs reconheceu 46 tipos de tricomas para as Melastomataceae neotropicais com o uso de MEV, e referiu 17 destes para o gênero Tibouchina. em Melastomataceae a morfologia dos tricomas tem sido extensivamente usada na delimitação dos táxons, assim como em estudos que antecederam ao trabalho de Cogniaux, a monografia das Melastomataceae brasileiras publicada em 1885. em Tibouchina sect. Pleroma a morfologia dos tricomas foi substancial para a circunscrição de várias espécies. O uso da MEV permitiu uma caracterização dos 15 tipos diferentes de tricomas observados nas 41 espécies examinadas. Os diferentes tipos são descritos com base no aspecto morfológico tanto em MO como em MEV e ilustrados através de eletromicrografias de varredura e fotomicrografias.

Anatomia de escapos, folhas e brácteas de Syngonanthus sect. Eulepis (Bong. ex Koern.) Ruhland (Eriocaulaceae)

Estudou-se a anatomia de escapos, folhas e brácteas de 24 espécimes de Syngonanthus sect. Eulepis, que ocorrem nos campos rupestres do Brasil. Os escapos apresentam número variado de costelas, epiderme unisseriada, com células de paredes totalmente espessadas; córtex com esclerênquima e parênquima clorofiliano alternados; endoderme contínua ou descontínua; periciclo estrelado; feixes vasculares colaterais; medula com células de paredes finas ou espessadas. As folhas e as brácteas apresentam epiderme com células de paredes total ou parcialmente espessadas, estômatos na face abaxial, margem com parênquima clorofiliano ou esclerênquima; mesofilo com hipoderme constituída de esclerênquima ou parênquima aqüífero, feixes vasculares colaterais envolvidos externamente pela endoderme e internamente pelo periciclo. Escapos, folhas e brácteas de Syngonanthus sect. Eulepis apresentam células com paredes espessadas e grande quantidade de esclerênquima, provavelmente como resposta adaptativa dessas plantas ao vento e à radiação excessiva comum nos campos rupestres. Epiderme com células de paredes espessadas, estômatos com câmara subestomática não especializada, presença de hipoderme, esclerênquima, e parênquima clorofiliano compacto, caracterizam anatomicamente escapos, folhas e brácteas de Syngonanthus sect. Eulepis. No geral, os caracteres anatômicos não são consistentes para separar os táxons dentro da seção.

Embryology and seed development of Paepalanthus sect. Actinocephalus (Koern.) Ruhland (Eriocaulaceae)

The embryology and seed structure of Paepalanthus sect. Actinocephalus species were studied. The embryological and structural seed characters fit well with those of the other commelinaceous families. Within the Commelinales sensu Dahlgren, Eriocaulaceae and Xyridaceae represent two embryologically close families. In Paepalanthus sect. Actinocephalus the ovule is orthotropus, bitegmic, and tenuicellate with a micropyle formed by the inner integument. The seeds are endotestal. The outer cell layer of the testa and the outer periclinal wall of the endotesta disintegrate during development. The endotegmen is tanniniferous. The outer layer of the tegmen becomes compressed and is no longer recognizable in the mature seed. The seeds are operculate.

A revision of Leptogium species with spherical-celled hairs (section Mallotium p.p.)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Seed morphology of bladderworts: a survey on Utricularia sect. Foliosa and sect. Psyllosperma (Lentibulariaceae) with taxonomic implications

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Purificação, imobilização e caracterização bioquímica de lipase produzida por Penicillium sect. Gracilenta CBMAI 1583 em cultivo submerso

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Mormonism and the Mormons : a historical view of the rise and progress of the sect self-styled Latter-Day Saints /

Mode of access: Internet.

Mormonism and the Mormons; a historical view of the rise and progress of the sect self-styled Latter-day saints.

Mode of access: Internet.

Pyrimidine-5'-nucleotidase Campinas, A New Mutation (p.r56g) In The Nt5c3 Gene Associated With Pyrimidine-5'-nucleotidase Type I Deficiency And Influence Of Gilbert's Syndrome On Clinical Expression.

Pyrimidine-5'-nucleotidase type I (P5'NI) deficiency is an autosomal recessive condition that causes nonspherocytic hemolytic anemia, characterized by marked basophilic stippling and pyrimidine nucleotide accumulation in erythrocytes. We herein present two African descendant patients, father and daughter, with P5'N deficiency, both born from first cousins. Investigation of the promoter polymorphism of the uridine diphospho glucuronosyl transferase 1A (UGT1A) gene revealed that the father was homozygous for the allele (TA7) and the daughter heterozygous (TA6/TA7). P5'NI gene (NT5C3) gene sequencing revealed a further change in homozygosity at amino acid position 56 (p.R56G), located in a highly conserved region. Both patients developed gallstones; however the father, who had undergone surgery for the removal of stones, had extremely severe intrahepatic cholestasis and, liver biopsy revealed fibrosis and siderosis grade III, leading us to believe that the homozygosity of the UGT1A polymorphism was responsible for the more severe clinical features in the father. Moreover, our results show how the clinical expression of hemolytic anemia is influenced by epistatic factors and we describe a new mutation in the P5'N gene associated with enzyme deficiency, iron overload, and severe gallstone formation. To our knowledge, this is the first description of P5'N deficiency in South Americans.

Crystal Structure Of (3e)-3-[(4-nitro-phen-oxy)-meth-yl]-4-phenyl-but-3-en-2-one.

In the title compound, C17H15NO4, the conformation about the C=C double bond [1.348 (2) Å] is E with the ketone group almost co-planar [C-C-C-C torsion angle = 7.2 (2)°] but the phenyl group twisted away [C-C-C-C = 160.93 (17)°]. The terminal aromatic rings are almost perpendicular to each other [dihedral angle = 81.61 (9)°] giving the mol-ecule an overall U-shape. The crystal packing feature benzene-C-H⋯O(ketone) contacts that lead to supra-molecular helical chains along the b axis. These are connected by π-π inter-actions between benzene and phenyl rings [inter-centroid distance = 3.6648 (14) Å], resulting in the formation of a supra-molecular layer in the bc plane.

Crystal Structure Of (3e)-3-(2,4-di-nitro-phen-oxy-meth-yl)-4-phenyl-but-3-en-2-one.

In the title compound, C17H14N2O6, the conformation about the C=C double bond [1.345 (2) Å] is E, with the ketone moiety almost coplanar [C-C-C-C torsion angle = 9.5 (2)°] along with the phenyl ring [C-C-C-C = 5.9 (2)°]. The aromatic rings are almost perpendicular to each other [dihedral angle = 86.66 (7)°]. The 4-nitro moiety is approximately coplanar with the benzene ring to which it is attached [O-N-C-C = 4.2 (2)°], whereas the one in the ortho position is twisted [O-N-C-C = 138.28 (13)°]. The mol-ecules associate via C-H⋯O inter-actions, involving both O atoms from the 2-nitro group, to form a helical supra-molecular chain along [010]. Nitro-nitro N⋯O inter-actions [2.8461 (19) Å] connect the chains into layers that stack along [001].

Preserved Fertility In A Patient With Gynecomastia Associated With The P.pro695ser Mutation In The Androgen Receptor.

The androgen insensitivity syndrome (AIS) is described as a dysfunction of the androgen receptor (AR) in 46,XY individuals, which can be associated with mutations in the AR gene or can be due to unknown mechanisms. Different mutations in AIS generally cause variable phenotypes that range from a complete hormone resistance to a mild form usually associated with male infertility. The purpose of this study was to search for mutations in the AR gene in a fertile man with gynecomastia and to evaluate the influence of the mutation on the AR transactivation ability. Sequencing of the AR gene revealed the p.Pro695Ser mutation. It is located within the AR ligand-binding domain. Bioinformatics analysis indicated a deleterious role, which was verified after testing transactivation activity and N-/C-terminal (N/C) interaction by in vitro expression of a reporter gene and 2-hybrid assays. p.Pro695Ser showed low levels of both transactivation activity and N/C interaction at low dihydrotestosterone (DHT) conditions. As the ligand concentration increased, both transactivation activity and N/C interaction also increased and reached normal levels. Therefore, this study provides functional insights for the p.Pro695Ser mutation described here for the first time in a patient with mild AIS. The expression profile of p.Pro695Ser not only correlates to the patient's phenotype, but also suggests that a high-dose DHT therapy may overcome the functional deficit of the mutant AR.

Glicoproteína-P, resistência a múltiplas drogas (MDR) e relação estrutura-atividade de moduladores

Multidrug resistance, MDR is a major obstacle for cancer chemotherapy. MDR can be reversed by drugs that vary in their chemical structure and main biological activity. Many efforts have been done to overcome MDR based on studies of structure-activity relationships and in this review we summarize some aspects of MDR mediated by P-glycoprotein (P-gp), as the most experimentally and clinically tested form of drug resistance. The most significant MDR mechanisms revealed until now are shortly discussed. Physicochemical and structural properties of MDR modulators, measures of the MDR reversal, and QSAR studies are included.