Sex attractant of the larch bud moth found by electroantennogram method

Zusammenfassung Mit Hilfe der Antennogramm-Methode wurdetrans-11-Tetracedenylacetat als spezifisches Attraktans für Männchen des LärchenwicklersZeiraphera diniana bestimmt. In geeigneter Konzentration ist die Attraktivität der synthetischen Substanz derjenigen virginer Weibchen ebenbürtig.

---

---

This research was supported in part by Environmental Protection Agency Grant No. EP-00802 and by the Rockefeller Foundation.

---

Contribution No. 46 of the research team for the investigation of the population dynamics of the larch bud moth, directed by Professor Dr.P. Bovey. The research was aided by the Swiss National Funds for Scientific Research.     

Effect of aluminium phosphate gel on whole-body retention of simultaneously administered226Ra,85Sr and47Ca in mice

Résumé L'administration presque simultanée d'un gel de phosphate d'alumine et de²²⁶RaCl₂ réduit de 800 fois l'absorption intestinale du²²⁶Ra chez la souris. La charge corporelle en⁸⁵Sr et⁴⁷Ca est réduite d'environ 10 resp. 3 fois.     

Suppression of immunization to tuberculosis and diphtheria by an extract of lymphoid tissue

Zusammenfassung Dank einer neuen Anwendung von Lymphknotenextrakten (statt Röntgenextrakten, Corticosteroiden, Antilymphozytenserum usw.) wird eine erhebliche Reduktion der immunologischen Reaktion erzielt, wenn die Tiere mit diesen Extrakten vorbehandelt und gleichzeitig mit Antigenen behandelt werden.

---

---

This investigation was supported in part by U.S.P.H.S. Research Grant No. CA-02624 from National Cancer Institute; and in part by an institutional grant to Detroit Institute of Cancer Research from United Foundation of greater Detroit allocated through Michigan Cancer Foundation and the Detroit General Hospital Research Corporation, and Newaygo County Cancer Society.     

Granular physics: creating a dry variety of quicksand

Sand can normally support a weight by relying on internal force chains. Here we weaken this force-chain structure in very fine sand by allowing air to flow through it: we find that the sand can then no longer support weight, even when the air is turned off and the bed has settled--a ball sinks into the sand to a depth of about five diameters. The final depth of the ball scales linearly with its mass and, above a threshold mass, a jet is formed that shoots sand violently into the air.     

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

CHARGE syndrome is a common cause of congenital anomalies affecting several tissues in a nonrandom fashion. We report a 2.3-Mb de novo overlapping microdeletion on chromosome 8q12 identified by array comparative genomic hybridization in two individuals with CHARGE syndrome. Sequence analysis of genes located in this region detected mutations in the gene CHD7 in 10 of 17 individuals with CHARGE syndrome without microdeletions, accounting for the disease in most affected individuals.     

Requirement of Src kinases Lyn, Hck and Fgr for BCR-ABL1-induced B-lymphoblastic leukemia but not chronic myeloid leukemia

The Abl kinase inhibitor imatinib mesylate is the preferred treatment for Philadelphia chromosome-positive (Ph(+)) chronic myeloid leukemia (CML) in chronic phase but is much less effective in CML blast crisis or Ph(+) B-cell acute lymphoblastic leukemia (B-ALL). Here, we show that Bcr-Abl activated the Src kinases Lyn, Hck and Fgr in B-lymphoid cells. BCR-ABL1 retrovirus-transduced marrow from mice lacking all three Src kinases efficiently induced CML but not B-ALL in recipients. The kinase inhibitor CGP76030 impaired the proliferation of B-lymphoid cells expressing Bcr-Abl in vitro and prolonged survival of mice with B-ALL but not CML. The combination of CGP76030 and imatinib was superior to imatinib alone in this regard. The biochemical target of CGP76030 in leukemia cells was Src kinases, not Bcr-Abl. These results implicate Src family kinases as therapeutic targets in Ph(+) B-ALL and suggest that simultaneous inhibition of Src and Bcr-Abl kinases may benefit individuals with Ph(+) acute leukemia.     

The knockout mouse project

Mouse knockout technology provides a powerful means of elucidating gene function in vivo, and a publicly available genome-wide collection of mouse knockouts would be significantly enabling for biomedical discovery. To date, published knockouts exist for only about 10% of mouse genes. Furthermore, many of these are limited in utility because they have not been made or phenotyped in standardized ways, and many are not freely available to researchers. It is time to harness new technologies and efficiencies of production to mount a high-throughput international effort to produce and phenotype knockouts for all mouse genes, and place these resources into the public domain.