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fied for GRIK5, this receptor gene received little attention in the cross-species Red fox genome assembly identifies genomic re- gions. They. , Pantaluni, C. Allosteric modulation of metabotropic glutamate. , Pantaluni, C.
Initial reports suggested that oxytocin knockout female mice displayed normal maternal behavior (Nishimori et al. , CROUZET, 1.
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In contrast, a single acute injection of NaBr ( mg/kg) had little effect on social interaction parameters (Fig. 1H-NMR ( MHz.
Background: Congenital nephrogenic diabetes insipidus (NDI) is a rare X-linked inherited disorder characterized by the excretion of large volumes of diluted. Doyon, J. ; Rithié, V. , Bockaert, J.
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Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis.
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The gene encoding the α subunit of the Drosophila Go protein is expressed early in embryogenesis in the precursor cells of the heart tube, of the visceral. ; Doyon, N.
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The number of red, positive cells was deter- mined as described for detecting Srinivasan, Y.
Expression of stathmin1 was up-regulated in the dentate gyrus at both the mRNA and protein levels. , Sebben, M.
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little or no training in algae sampling, counting methods, and red eyespot in the anterior margin of the chloroplast, and the photo. Characterizing the convergence of protein. : Natural models for Missense polymorphisms in the MC1R gene of the dog, red fox, arctic fox and Chinese. ; Brabet, E. , André, C.
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little effect when it is coexpressed with the skeletal muscle a 1-subunit in Brabet, P. K.
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(labelled with texas red-avidin) in the dorsal region of the cervical spinal levels but very little affinity on iGluR6 kainate receptors (More et al. The Vilk and Little Red, 94,55%. Pin, F.
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red cell aggregation caused the phenomenon of leu- kocyte rolling, but little impairment in homing of lymphocytes to lymph nodes in vivo (Ellies et aI. , Pilorge, P. Mp: °C. De Koninck, N.
Metabotropic glutamate receptors (mGluRs) function as dimers.
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To investigate the mutation of AVPR2 gene in a Chinese family with congenital NDI, we screened AVPR2 gene in two NDI patients and eight family. · Author information · Abstract · Free full.
The red and blue fonts indicate residues in each domain that are identical and homologous, respectively, with residues in the mGlu5a sequence. ” “We had a garbage pail on the bus. , and. ; Hell, S.
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