Article
True vs. false inv(Y)(p11q11.2): A familial instance concurrent with trisomy 21
Fecha
2012Autor
Pisarchik, A.N.
Jaimes-Reategui, R.
Sevilla-Escoboza, J.R.
Ruiz-Oliveras, F.R.
García-Lopez, J.H.
Institución
Resumen
We propose and implement experimentally an opto-electronic chaotic communication system based on chaos synchronization, which uses two channels: the electronic channel for synchronization and the optical channel for information transmission. Both the transmitter and the receiver contain identical chaotic Rossler-like electronic circuits and identical continuous wave semiconductor lasers. The circuit in the receiver is synchronized with the circuit in the transmitter by one of the variables via the electronic channel, while another variable serves to drive the laser pump current chaotically. Due to the functional dependence of the circuit variables, the signals transmitted through the electronic and optical channels are also functionally dependent. A message is encrypted into the laser output in the transmitter and sent to the receiver via the optical channel, where the received waveform is compared with the laser output in the receiver. Since the lasers in the transmitter and in the receiver are completely synchronized, the message is retrieved with a very good precision. " 2012 The Franklin Institute.",,,,,,"10.1016/j.jfranklin.2012.10.005",,,"http://hdl.handle.net/20.500.12104/45519","http://www.scopus.com/inward/record.url?eid=2-s2.0-84870060164&partnerID=40&md5=fd988ee09fad2f0aee22a430e56eea45",,,,,,"10",,"Journal of the Franklin Institute",,"3194 3202",,"349",,"Scopus WOS",,,,,,,,,,,,"Two-channel opto-electronic chaotic communication system",,"Article"
"47264","123456789/35008",,"García-Cruz, D., Division de Genetica, Subjefatura de Investigation Cientifica, Unidad de Investigacion Biomedica, Centro Medico de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Mexico; García-Esquivel, L., Division de Genetica, Subjefatura de Investigation Cientifica, Unidad de Investigacion Biomedica, Centro Medico de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Mexico; Rivera, H., Division de Genetica, Subjefatura de Investigation Cientifica, Unidad de Investigacion Biomedica, Centro Medico de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Mexico",,"García-Cruz, D. García-Esquivel, L. Rivera, H.",,"1985",,"A 10 10/12 year-old boy with a de novo t(11;15) (q25;q23) leading to trisomy 15q23?pter was studied. The clinical features were compatible with other cases of distal trisomy 15q. The critical segment for this trisomy is tentatively assigned to bands 15q25?qter.",,,,,,,,,"http://hdl.handle.net/20.500.12104/45485","http://www.scopus.com/inward/record.url?eid=2-s2.0-0022413066&partnerID=40&md5=45edecd5594a1bdd236a583d4208ec0b",,,,,,"3",,"Annales de Genetique",,"192 196",,"28",,"Scopus",,,,,,,,,,,,"Trisomy 15q23?qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment",,
"47292","123456789/35008",,"González-Villarreal, L.M., Instituto de Botánica, Universidad de Guadalajara, Apartado Postal 139, Zapopan, Jalisco 45110, Mexico, Department of Botany, University of Wisconsin, 430 Lincoln Drive, Madison, WI 53706-1381, United States",,"Gonzalez-Villarreal, L.M.",,"2003",,"Two new species of oak (Fagaceae) with narrowly elliptic-lanceolate leaves from the Sierra Madre del Sur of western Jalisco, Mexico, are described and illustrated. Quercus cualensis is a local endemic and Q. iltisii a more widespread species; they are closely related to Q. salicifolia Nee.",,,,,,,,,"http://hdl.handle.net/20.500.12104/45513","http://www.scopus.com/inward/record.url?eid=2-s2.0-0038046356&partnerID=40&md5=01a907182d12b1607ab9e1c93bd9fabd http://dx.doi.org/10.1663/0007-196X(2003)055[0049:TNSOOF]2.0.CO;2",,,,,,"1",,"Brittonia",,"49 60",,"55",,"Scopus WOS BioOne",,,,,,"Endemic; Fagaceae; Mexico; Oaks; Quercus",,,,,,"Two new species of oak (Fagaceae, Quercus sect. Lobatae) from the Sierra Madre del Sur, Mexico",,"Article"
"47269","123456789/35008",,"Rivera, H., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Gutiérrez-Angulo, M., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Gómez-Sánchez, H., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico; Macías-Gómez, N., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico; Barros-Núñez, P., División De Genética, Instituto Mexicano del Seguro Social, Ap. Postal 1-3838, Guadalajara, Jalisco, Mexico, Doctorado En Genética Humana, Universidad De Guadalajara, Guadalajara, Jalisco, Mexico",,"Rivera, H. Gutierrez-Angulo, M. Gomez-Sanchez, H. Macias-Gomez, N. Barros-Nunez, P.",,"2002",,"A boy with Down syndrome due to a free trisomy 21 also had a metacentric Y chromosome with an arm euchromatic and the other heterochromatic inherited from his phenotypically normal father. This chromosome was mitotically stable and hybridized with the DYZ3 probe precisely at its primary constriction; in addition, a subtelomeric Xp/Yp probe gave the expected signal near the end of the euchromatic arm. So, the proband's karyotype was 47,X,inv(Y)(p11q11.2),+21. Given the high frequency of both chromosome anomalies, we regard its concurrence as a mere coincidence. This observation, along with previous reports, allows us to classify the apparent pericentric inversions of the Y chromosome into two types: "true" inversions characterized by an alphoid single centromere and mitotic stability, and "false" inversions in which a nonalphoid centromere has taken over the usual alphoid centromere; indeed, these chromosomes are dicentric and mitotically unstable. Finally, the inv(Y) polymorphism in man compares with that documented in other mammal species, in which the rearranged Y chromosome neither impairs the fertility nor has other phenotypical consequences. " 2002 editions scientifiques et médicales Elsevier SAS. All rights reserved.