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1.
Genetic polymorphisms and intrauterine development. Evidence of decreased heterozygosity in light-for-dates human newborn babies 总被引:2,自引:0,他引:2
E. Bottini F. Gloria-Bottini P. Lucarelli A. Polzonetti F. Santoro A. Varveri 《Cellular and molecular life sciences : CMLS》1979,35(12):1565-1567
Summary In 2 independent samples of low-birth-weight infants the proportion of females and homozygotes for a series of polymorphic systems was higher in light-for-dates than in preterm babies. The observation seems to give support to the hypothesis that homozygosity for normal polymorphisms may decrease in general intrauterine growth rate. Since it is known that survival rate is strongly related to birth weight, a correlation between growth retardation and homozygosity may have a major role in the maintenance of such polimorphisms.We thank Prof. L. Ginzburg for helpful comments. 相似文献
2.
Riassunto Gli Autori dimostrano che lo spettro di diffrazione a basso angolo del tessuto osseo è determinato da micelle elissoidali (elissoidi di rivoluzione) delle dimensioni di 200 × 70 Å, pertinenti all'osseina e accolte in incavi delimitati dalla frazione inorganica. 相似文献
3.
Summary It is reported that Ca2+-induced discharge of in situ nematocytes of acontia ofCalliactis parasitica can occur by cell-to-cell transmission along the acontial filament at a speed that averages 9.8·10–3 cm–1. The discharge is preceded by protrusion of nematocytes that proceeds along the acontium at a slightly higher speed. 相似文献
4.
Molecular mechanism of cAMP modulation of HCN pacemaker channels. 总被引:26,自引:0,他引:26
Hyperpolarization-activated cation channels of the HCN gene family contribute to spontaneous rhythmic activity in both heart and brain. All four family members contain both a core transmembrane segment domain, homologous to the S1-S6 regions of voltage-gated K+ channels, and a carboxy-terminal 120 amino-acid cyclic nucleotide-binding domain (CNBD) motif. Homologous CNBDs are responsible for the direct activation of cyclic nucleotide-gated channels and for modulation of the HERG voltage-gated K+ channel--important for visual and olfactory signalling and for cardiac repolarization, respectively. The direct binding of cyclic AMP to the cytoplasmic site on HCN channels permits the channels to open more rapidly and completely after repolarization of the action potential, thereby accelerating rhythmogenesis. However, the mechanism by which cAMP binding modulates HCN channel gating and the basis for functional differences between HCN isoforms remain unknown. Here we demonstrate by constructing truncation mutants that the CNBD inhibits activation of the core transmembrane domain. cAMP binding relieves this inhibition. Differences in activation gating and extent of cAMP modulation between the HCN1 and HCN2 isoforms result largely from differences in the efficacy of CNBD inhibition. 相似文献
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Cornea regeneration in the Pacific giant octopus,Octopus dofleini,and the common octopus,O. vulgaris
Summary Cornea regeneration in a Pacific giant octopus,Octopus dofleini, occurred within 10 days after the injury was observed. Surgical removal of the cornea in 2 common octopi,O. vulgaris experimentally duplicated this cornea regeneration within a 10-day period. It is, therefore, concluded that besides sucking discs, arms, and nerve fibres, octopi can also regenerated corneal tissue.The authors would like to thank U. E. Friese, B. Borowski, P. Burn, J.W. Atz, G.J. Nelson, H. Feinberg, P. Fenimore, C. Roper, M. Nixon, M. Segalla, G. Clark, D.O. Calligaro, J.M. Anderson and R.J. Koestler for assistance and advice. Illustrations were drawn by G.D. This work was supported by the New York Aquarium of the New York Zoological Society, while G.D. was at the New York Aquarium. 相似文献
8.
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria. 总被引:22,自引:0,他引:22
J N Spelbrink F Y Li V Tiranti K Nikali Q P Yuan M Tariq S Wanrooij N Garrido G Comi L Morandi L Santoro A Toscano G M Fabrizi H Somer R Croxen D Beeson J Poulton A Suomalainen H T Jacobs M Zeviani C Larsson 《Nature genetics》2001,28(3):223-231
The gene products involved in mammalian mitochondrial DNA (mtDNA) maintenance and organization remain largely unknown. We report here a novel mitochondrial protein, Twinkle, with structural similarity to phage T7 gene 4 primase/helicase and other hexameric ring helicases. Twinkle colocalizes with mtDNA in mitochondrial nucleoids. Screening of the gene encoding Twinkle in individuals with autosomal dominant progressive external ophthalmoplegia (adPEO), associated with multiple mtDNA deletions, identified 11 different coding-region mutations co-segregating with the disorder in 12 adPEO pedigrees of various ethnic origins. The mutations cluster in a region of the protein proposed to be involved in subunit interactions. The function of Twinkle is inferred to be critical for lifetime maintenance of human mtDNA integrity. 相似文献
9.
Ligand recognition by the I domain-containing integrins 总被引:11,自引:0,他引:11
Seven of the integrin α subunits described to date, α
1 , α
2 , α
L , α
X , α
d , α
M and α
E , contain a highly conserved I (or A) domain of approximately 200 amino acid residues inserted near the amino-terminus of
the subunit. As the result of a variety of independent experimental approaches, a large body of data has recently accumulated
that indicates that the I domains are independent, autonomously folding domains capable of directly binding ligands that play
a necessary and important role in ligand binding by the intact integrins. Recent crystallographic studies have elucidated
the structures of recombinant α
M and α
L I domains and also delineated a novel divalent cation-binding motif within the I domains (metal ion-dependent adhesion site,
MIDAS) that appears to mediate the divalent cation binding of the I domains and the I domain-containing integrins to their
ligands. 相似文献
10.
Gerald F. Shields Gregory M. Clausen Christina S. Marchion Tracy L. Michel Kathryn C. Styren Callie N. Riggin Tonya D. Santoro Lindee M. Strizich 《西北部美国博物学家》2011,67(1)
At least 5 sibling species and an additional 11 cytotypes of the Simulium arcticum complex occur in Montana. Consequently, this speciose complex might allow study of environmental correlates with genetic differentiation. We used conventional methods of collection and cytogenetic analysis to study 1128 male larvae of the Simulium arcticum complex at 15 sites within 5 drainages in western Montana to test the hypothesis that distribution of siblings is associated with elevation. We sampled at the mouth, at the headwaters, and at an intermediate site to span the range of elevations within each drainage. We restricted our analyses to the most abundant taxa of the S. arcticum complex within our study area and observed a statistically significant presence of S. apricarium at low-elevation sites. Simulium arcticum IIL-18 appeared more frequently than expected at high elevation sites. Simulium brevicercum and S. arcticum sensu strictu appeared to be distributed randomly. We suggest potential causal reasons for these distributions including differential use of habitats along these elevational gradients. 相似文献