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3 This study will help to establish if such disease modifying effects will be evident in human subjects also.
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The authors point out that while limited studies have been done in humans, due to the lack of selective D1/D5 compounds available for human use, studies with non-selective compounds suggest that an "inverted-U" response may be evident in humans as well as animals.
This basal pro-apoptotic function of JNK1 is evident in human epithelial cancer cells (but not in non-cancer cells) and is constitutively inhibited by endogenous JNK2.
This "active search for regularity" is considered a universal process [5] that cuts across sensory modalities [6], [7] and is evident in human neonates [8], non-human primates [9] and rodents [10].
The gene expression of TRPM4, TRPM7, and GAPDH was evident in human atrial myocytes.
Intratumoural heterogeneity is evident in human cancers and most likely contributes to differing chemotherapeutic responses.
A similar phenomenon is evident in human Burkitt's lymphoma cell lines.
Two alternative splicing isoforms containing a 75-aa N-terminal truncation were evident in human CPEB1 (Fig. 1D).
For example, the currently available animal models are limited in their capacity to produce the metabolic alterations which are evident in human pre-eclamptic pregnancies [ 41, 42].
RT-PCR and Western immunoblot analysis revealed that in addition to TRPM4, TRPM7 channel current, mRNA and protein expression were evident in human atrial myocytes.
Dysfunction of the immune system is evident in human immunodeficiency virus (HIV -patients, even from tHIV -patientseven the HIV infromion.
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