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1 foods remain to be evaluated in light of CYP pharmacogenetics.
2 l implementation of clopidogrel and warfarin pharmacogenetics.
3 edicine, and future clinical implications of pharmacogenetics.
4 obehavioral mechanisms of naltrexone and its pharmacogenetics.
5 h particular design features of relevance in pharmacogenetics.
6  with, previous findings in antihypertensive pharmacogenetics.
7        We provide a current review of opiate pharmacogenetics.
8 tcomes, which are of particular relevance in pharmacogenetics.
9 mechanism of action will lead to advances in pharmacogenetics.
10 could link to normal reversal learning using pharmacogenetics.
11 ashion, and by combining this with selective pharmacogenetic activation and optogenetic mapping techn
12 ns to ambient temperature changes, and their pharmacogenetic activation drives robust suppression of
13                                              Pharmacogenetic activation of c-Fos-labelled sleep-activ
14                                              Pharmacogenetic activation of Mrgprb4-expressing neurons
15                                    Moreover, pharmacogenetic activation of Nos1(PVH) neurons suppress
16 changes of L5 PNs are prevented by selective pharmacogenetic activation of PV+INs in the barrel corte
17                                              Pharmacogenetic activation of somatostatin-expressing ce
18                                              Pharmacogenetic activation of the mouse CT equivalent ha
19                                 Furthermore, pharmacogenetic activation of these neurons using design
20 antly more accurate (all p < 0.001) with the pharmacogenetic algorithm (52%) than with all other meth
21              Furthermore, we developed a new pharmacogenetic algorithm that permits the stratificatio
22 n dose stratified by genotype), and 1 formal pharmacogenetic algorithm, using both clinical and genet
23 d Clinical Effectiveness Trial Comparing Two Pharmacogenetic Algorithms and Standard Care for Individ
24                                              Pharmacogenetic algorithms based on regression equations
25 re the accuracy of genetic tables and formal pharmacogenetic algorithms for warfarin dosing.
26  demonstrate that racially informed warfarin pharmacogenetic algorithms perform better than tradition
27  conducting 1000 simulations of the applying pharmacogenetic algorithms to individualize dosing of wa
28 arin dose better than empiric dosing, formal pharmacogenetic algorithms were the most accurate.
29 eclinical trial design of target population, pharmacogenetic algorithms, and dosing protocols to opti
30             This study evaluated the largest pharmacogenetic AMD cohort reported to date.
31                                              Pharmacogenetic analysis in the placebo controlled trial
32                      The authors performed a pharmacogenetic analysis of antipsychotic treatment resp
33                              This study is a pharmacogenetic analysis of the effects of genetic varia
34 evalence (<2%) of most variants hinder their pharmacogenetic analysis with population sizes often ina
35                                              Pharmacogenetics analysis showed single nucleotide polym
36                                              Pharmacogenetics analysis showed that exm-rs1321744 achi
37                      Of these, 15 genetic, 2 pharmacogenetic and 6 biochemical studies were included
38 lysis of candidate gene association studies, pharmacogenetic and biochemical (metabolomics) studies p
39 we found that there were not enough genetic, pharmacogenetic and biochemical studies of ADHD in adult
40 Ca(2)(+) and glutamate indicators as well as pharmacogenetic and electrical control of neurotransmitt
41                             Pharmacological, pharmacogenetic and environmental approaches to prevent
42 on of neuronal CB2Rs, as shown by a combined pharmacogenetic and immunohistochemical approach.
43 sleep-wake regulation in humans and combined pharmacogenetic and neurophysiologic methods to analyze
44 in the time in therapeutic range between the pharmacogenetic and standard arm (78.8% versus 73.8%; P=
45 or candidate gene association studies, 5 for pharmacogenetics and 21 for biochemical studies.
46 ncluding histocompatibility, immunogenetics, pharmacogenetics and anthropology studies, among many ot
47                    This review will focus on pharmacogenetics and pharmacogenomics and their role in
48 f AA in patients treated with TNF inhibitors.Pharmacogenetics and the inherent physiologic levels of
49                                 First, using pharmacogenetics and two-photon calcium imaging, we vali
50                                              Pharmacogenetics and, more recently, pharmacogenomics ha
51 ocompatibility, immunology, epidemiology and pharmacogenetics) and population genetics.
52  clinical pharmacology, pharmacokinetics and pharmacogenetics, and biostatistics and a patient repres
53 n microscopy, morphological reconstructions, pharmacogenetics, and diffusible dye, calcium, and gluta
54 ate with advances in genetics, genomics, and pharmacogenetics; and how they can apply this knowledge
55                         Therefore, we used a pharmacogenetic approach based on a virus-mediated expre
56 ulation of sleep/wakefulness and highlight a pharmacogenetic approach for the amelioration of narcole
57 d, we evaluated the feasibility of a reverse pharmacogenetic approach in a preclinical mouse model.
58                                    We used a pharmacogenetic approach in mice to diminish MD neuron a
59 we bypass this lethality using a noninvasive pharmacogenetic approach to inducibly perturb neuron act
60                                      Using a pharmacogenetic approach to model MD hypofunction, we re
61                    The authors propose a new pharmacogenetic approach using ondansetron to treat seve
62 eptor exclusively activated by designer drug pharmacogenetic approach, transient inhibition of MeA PT
63                                      Using a pharmacogenetic approach, we find PKMzeta-antisense in h
64                                      Using a pharmacogenetic approach, we find that mTOR-dependent ph
65 lbumin interneurons in the mPFC with a novel pharmacogenetic approach, we restored gamma-aminobutyric
66                                      Using a pharmacogenetic approach, we show that the predicted Dro
67 eptor exclusively activated by designer drug pharmacogenetic approach.
68 between correlation and causality, we used a pharmacogenetic approach.
69                                 This study's pharmacogenetics approach strongly implicates the role o
70 ORC1 activity in the adult brain, we used a "pharmacogenetic" approach that relies on the synergistic
71 ethodologically, these results highlight how pharmacogenetic approaches allow neuron function to be q
72                            Here, we used two pharmacogenetic approaches in transgenic mice to selecti
73                          In the near future, pharmacogenetic approaches may facilitate personalized p
74 tions of molecular genetic, optogenetic, and pharmacogenetic approaches that overcome previous limita
75 ults highlight the requirement for stringent pharmacogenetic approaches to separate specific on-targe
76                              Optogenetic and pharmacogenetic approaches were used to bidirectionally
77 and subunit-specific deletion, combined with pharmacogenetic approaches, demonstrate that amygdala ex
78 ur findings advance the understanding of the pharmacogenetic architecture of statin response.
79  REVIEW: The fields of clinical genetics and pharmacogenetics are rapidly expanding.
80 70.6% and 72.2% (P=0.47) in the standard and pharmacogenetic arms, respectively.
81                  We identified a significant pharmacogenetic association at SNP rs37972, replicated i
82      The CATT and IVAN data do not support a pharmacogenetic association between the 2 VEGFR2 SNPs, r
83  A previously published study demonstrated a pharmacogenetic association between the minor alleles of
84 anisms and the clinical implications of this pharmacogenetic association remain unknown.
85                  With the rapid emergence of pharmacogenetic association studies of single nucleotide
86                                              Pharmacogenetic association with anti-VEGF treatments ma
87 priori-selected candidate genes did not show pharmacogenetic associations above a chance level, but a
88         This study provides evidence that no pharmacogenetic associations exist between the studied V
89                                     Numerous pharmacogenetic associations have been discovered for im
90 unctional variants in GALR1 and to replicate pharmacogenetic associations is warranted.
91  The objectives were to replicate 3 reported pharmacogenetic associations of response in nAMD and to
92                              We investigated pharmacogenetic associations of the previously studied G
93          This review highlights the germline pharmacogenetic associations that are currently being us
94                                 We estimated pharmacogenetic associations using high-quality phenotyp
95                          The most consistent pharmacogenetic associations were observed for the corre
96 atment in neovascular AMD, suggesting strong pharmacogenetic associations with anti-VEGF treatment.
97 standing of pathogenic mechanisms underlying pharmacogenetic associations.
98  warfarin doses were prescribed according to pharmacogenetic-based algorithms for the first 5 days.
99                                              Pharmacogenetic-based dosing was associated with a highe
100 ational Warfarin Pharmacogenetics Consortium pharmacogenetic-based warfarin dosing algorithm (based o
101 y provides the first demonstration that host pharmacogenetics can influence therapeutic response in C
102 nes from participants of the Cholesterol and Pharmacogenetics (CAP) simvastatin clinical trial, we fo
103 ding rs7856096 to the International Warfarin Pharmacogenetic Consortium pharmacogenetic dosing algori
104 arin were obtained at International Warfarin Pharmacogenetics Consortium (IWPC) sites and the Univers
105 ntries as part of the International Warfarin Pharmacogenetics Consortium effort.
106 he recently published International Warfarin Pharmacogenetics Consortium pharmacogenetic-based warfar
107                            Rapid advances in pharmacogenetics, continuous decrease in genotyping cost
108                                      Growing pharmacogenetic data make it evident that many opiate-re
109 vity, there are relatively little actionable pharmacogenetic data with antiplatelet agents.
110 improving patient management on the basis of pharmacogenetic data.
111 parameters, drug interaction parameters, and pharmacogenetics data have been unevenly collected in di
112 g these barriers to routine incorporation of pharmacogenetics data into clinical care.
113                        Here application of a pharmacogenetic deactivation technique enabled us to inv
114                    Moreover, few studies use pharmacogenetic designs that permit testing of genotype
115                            Thus, NUDT15 is a pharmacogenetic determinant for thiopurine-induced leuko
116 m, and are largely independent of, the major pharmacogenetic determinants of rosuvastatin-induced LDL
117 omewide association study would reveal novel pharmacogenetic determinants of the response to inhaled
118                               The effects of pharmacogenetic determinants on platelet function and ca
119 eagents and has a great potential for future pharmacogenetic diagnostics and therapy.
120  cues, personality traits, neurochemical and pharmacogenetic differences.
121  Ca(2+) channel (CaV1.1 R174W) linked to the pharmacogenetic disorder malignant hyperthermia.
122 gnant hyperthermia (MH) is potentially fatal pharmacogenetic disorder of skeletal muscle caused by in
123                  Malignant hyperthermia is a pharmacogenetic disorder typically triggered by potent i
124 national Warfarin Pharmacogenetic Consortium pharmacogenetic dosing algorithm resulted in a 5.8 mg/we
125           Incorporation of this variant into pharmacogenetic dosing algorithms could improve warfarin
126         These findings may have an important pharmacogenetic effect on the development of new PAR ant
127 tion of platelet PAR1 function, but a strong pharmacogenetic effect was observed with the PAR4-specif
128 in the complement factor H (CFH) gene have a pharmacogenetics effect on the anti-vascular endothelial
129 tive of this study is to test the naltrexone pharmacogenetic effects of the Asn40Asp SNP in a sample
130                             We also examined pharmacogenetic effects on cognition in the context of a
131                                     We found pharmacogenetic evidence for a role of 5-HT in mediating
132                                        Thus, pharmacogenetic evidence suggests that increased 5-HT le
133                            Abcb5 alleles are pharmacogenetic factors that affect susceptibility to HI
134 ht the pharmacokinetic, pharmacodynamic, and pharmacogenetic factors that can influence analgesic, se
135  ERN and error positivity were unaffected by pharmacogenetic factors, but ERN was decoupled from beha
136                                          The pharmacogenetic findings also implicate the kainate rece
137                                        These pharmacogenetic findings are in contrast to observations
138 ar mixture of significant and nonsignificant pharmacogenetic findings that are sometimes consistent w
139 ch for PD and highlight the applicability of pharmacogenetics for enhancing cellular signaling in rep
140                                        Using pharmacogenetic gain- and loss-of-function studies, we f
141                                              Pharmacogenetics genetically re-engineers neurons to pro
142 n a few small studies relating to the use of pharmacogenetics-guided dosing in the initiation of warf
143             With its particular relevance to pharmacogenetic GWAS, SurvivalGWAS_SV will aid in the id
144  RECENT FINDINGS: Evidence now suggests that pharmacogenetics has a role in the effects of analgesic,
145    Since its first description, the field of pharmacogenetics has expanded to study a broad range of
146                                              Pharmacogenetics has led to the identification of severa
147 oncology, systematic application of efficacy pharmacogenetics has not been integrated into drug disco
148                                              Pharmacogenetics has offered compelling evidence toward
149                              The third area, pharmacogenetics, has utility for some therapies today.
150 ic cells and hosts (eg, pharmacokinetics and pharmacogenetics) have pushed the cure rate of childhood
151  integration of research on neuroimaging and pharmacogenetics holds promise for improving treatment f
152 techniques, such as excitability studies and pharmacogenetics, holds promise in elucidating the under
153                                              Pharmacogenetics identifies the likelihood of adverse ev
154  Substance dependence can be thought of as a pharmacogenetic illness, and most likely hundreds and mo
155 cogenomics Research Network and the Clinical Pharmacogenetics Implementation Consortium are partnersh
156 ical-subcortical networks in humans, and the pharmacogenetic implications of dopamine-related genes o
157  define the role of clopidogrel and warfarin pharmacogenetics in clinical practice.
158 ew Orleans in October 2012, Optogenetics and Pharmacogenetics in Neuronal Function and Dysfunction, b
159 drug pharmacokinetics, pharmacodynamics, and pharmacogenetics in view of the absence of easily measur
160                                              Pharmacogenetics in warfarin clinical trials have failed
161 ement strategies based on modifier genes, to pharmacogenetics, in which individual genetic informatio
162                                              Pharmacogenetic inactivation of FosB-expressing neuron e
163                                    Selective pharmacogenetic inactivation of these neurons inhibited
164   In this article, we provide an overview of pharmacogenetics, including pharmacokinetics (PK), pharm
165 tandardized dose escalation, and to evaluate pharmacogenetics influences on PK and PD parameters.
166                                              Pharmacogenetic inhibition of C1 neurons bilaterally res
167                          We investigated the pharmacogenetic interaction between A118G variation and
168        This study demonstrates a significant pharmacogenetic interaction between anti-IL-4 receptor a
169 nconsistent, suggesting the possibility of a pharmacogenetic interaction.
170 t effects of OPRM1 allelic variation, or for pharmacogenetic interactions between genotype and drug t
171 nctional variants on schizophrenia risk, and pharmacogenetic interactions of AKT1 with the effects on
172 esearch paradigms may be needed to translate pharmacogenetics into clinical tools.
173                                 In the first pharmacogenetic investigation of the efficacy of varenic
174                      This is the first large pharmacogenetic investigation of the inflammatory IL-4/I
175 rs of ICS response by conducting the largest pharmacogenetic investigation to date in 2672 ICS-treate
176                     A synthesis of opto- and pharmacogenetics is beginning to reveal how various inte
177                                              Pharmacogenetics is being used to develop personalized t
178                                              Pharmacogenetics is one example of how gene-environment
179  rare variants to detect and replicate novel pharmacogenetic loci.
180 on studies (GWAS) can rapidly identify novel pharmacogenetic loci.
181 ciation has identified the T gene as a novel pharmacogenetic locus for inhaled corticosteroid respons
182                                              Pharmacogenetic manipulation revealed the individual con
183 rkers for these neurons, and optogenetic and pharmacogenetic manipulations demonstrate that several p
184                   Our study discovered novel pharmacogenetic markers and provided detailed insight in
185  interest, our finding may aid in developing pharmacogenetic markers for ADHD.
186                   Three principle classes of pharmacogenetic markers have emerged: 1) pharmacokinetic
187 hesia and analgesia generated some hope that pharmacogenetics may guide anesthesiologists to provide
188  variants for monitoring treatment response (pharmacogenetics) may usher in a new era of personalized
189                            Here we perform a pharmacogenetic meta-analysis of genome-wide association
190                                    Opto- and pharmacogenetic methods have played an important role in
191                                        Using pharmacogenetic methods to conditionally ablate adult ne
192  these results indicate that a comprehensive pharmacogenetic model integrating NUDT15 variants may in
193 ress and inhibition of neurogenesis in a rat pharmacogenetic model.
194 electively inhibiting these neurons with the pharmacogenetic neuromodulator hM4D.
195  II- study (n = 745, age: 8-21, USA) and the Pharmacogenetics of adrenal suppression cohort (n = 391,
196 atric Asthma Gene Environment Study, and the Pharmacogenetics of Adrenal Suppression with Inhaled Ste
197                     While recent advances in pharmacogenetics of adverse drug reactions show promise,
198             Although preliminary work on the pharmacogenetics of alcoholism and its treatment has bee
199 med a meta-analysis of three cohort studies: Pharmacogenetics of Asthma Medication in Children: Medic
200 namics (colonic transit, bowel function) and pharmacogenetics of CDC in constipation-predominant irri
201                               In conclusion, pharmacogenetics of CFH Y402H polymorphism may play a ro
202 rge transfusion requirements and the complex pharmacogenetics of clopidogrel may have played a role.
203 will discuss the most recent developments in pharmacogenetics of commonly used perioperative medicati
204 stigated the population pharmacokinetics and pharmacogenetics of efavirenz in 307 patients coinfected
205 eliminary results of this pilot study on the pharmacogenetics of FcgammaR and biological therapy in p
206          We summarize recent progress in the pharmacogenetics of IBD with respect to partitioning pat
207                                          The pharmacogenetics of methotrexate (MTX) was investigated
208 dependence; however, less is known about the pharmacogenetics of smoking cessation.
209  to describe what has heretofore been called pharmacogenetics or chemicogenetics.
210 plicated by acute ketamine administration or pharmacogenetic parvalbumin-interneuron suppression.
211 ic ligand--GPCR pairs (aka DREADDs, RASSLS, 'pharmacogenetics') permits the study of pharmacology usi
212                                              Pharmacogenetics (PG) could improve dosing efficiency an
213                                              Pharmacogenetic/pharmacogenomic (PGx) approaches to psyc
214 ts are likely to have an important effect on pharmacogenetic phenotypes.
215 l implementation of clopidogrel and warfarin pharmacogenetics possible.
216 ine learning approaches for high-dimensional pharmacogenetic prediction, and for prediction of clinic
217   This study provides a platform to evaluate pharmacogenetic predictors of response or severe adverse
218                                              Pharmacogenetics primarily uses genetic variation to ide
219 that this hyperkinetic disorder has a unique pharmacogenetic profile.
220 3A5 gene is likely to contribute to multiple pharmacogenetic profiles across the continent.
221 s individual susceptibility, prognostic, and pharmacogenetic profiles to maximize the efficacy and mi
222 research settings for causal gene discovery, pharmacogenetic purposes, and gene-gene and gene-environ
223 ight deprivation blocks ODP and, conversely, pharmacogenetic reduction of PV cell firing rates can ex
224 ton magnetic resonance spectroscopy data and pharmacogenetic response to stimulant medication.
225 treated subjects, demonstrating a successful pharmacogenetic screen in MS.
226               In the realm of cardiovascular pharmacogenetics, significant advances have identified m
227 of optical activation and cell type-specific pharmacogenetic silencing in vitro, we found that dendri
228 on cell-type-specific optical activation and pharmacogenetic silencing in vitro, we show that tempora
229                                              Pharmacogenetic silencing of VMHvl reversibly inhibits i
230       Here, using optogenetic activation and pharmacogenetic silencing, we found that type 6 bipolar
231 an ancestry who participated in one of three pharmacogenetic smoking cessation clinical trials and we
232             Moreover, optogenetic as well as pharmacogenetic specific activation of the vHipp-mPFC pa
233                              Here, we used a pharmacogenetic strategy to decrease mediodorsal thalami
234 was performed on data from three genome-wide pharmacogenetic studies (the Genome-Based Therapeutic Dr
235                                              Pharmacogenetic studies aiming to personalize the treatm
236                                   Currently, pharmacogenetic studies are at an impasse as the low pre
237                                              Pharmacogenetic studies can be conducted in multicenter
238                                     To date, pharmacogenetic studies have been primarily performed in
239                         Importance: Previous pharmacogenetic studies have shown the prognostic impact
240 his assay may be useful to complement future pharmacogenetic studies in asthma.
241                                              Pharmacogenetic studies in larger cohorts are needed to
242 hese data may provide proof-of-principle for pharmacogenetic studies in schizophrenia.
243 NP-drug response association dataset for 650 pharmacogenetic studies involving 257 drugs in this upda
244                                              Pharmacogenetic studies of admixed ethnic groups have be
245 nally, the authors discuss unique aspects of pharmacogenetic studies that may distinguish them from s
246                                Although most pharmacogenetic studies to date have assessed the associ
247                                        Prior pharmacogenetic studies usually measure exposure via sin
248                           Additional, larger pharmacogenetic studies would help to validate these res
249 s: in vivo pharmacokinetics studies, in vivo pharmacogenetic studies, in vivo drug interaction studie
250                                   Concerning pharmacogenetic studies, no association was found for th
251 ed populations, which can be used for future pharmacogenetic studies.
252 ance of maximizing adherence to treatment in pharmacogenetic studies.
253                                              Pharmacogenetics studies are the platform for discoverin
254 rom non-responders via genetic predictors in pharmacogenetics studies have not met their anticipated
255 ssion Network [DeNT] study; N=332), and 3) a pharmacogenetic study (the Genome-Based Therapeutic Drug
256                                         This pharmacogenetic study evaluated the impact of high-risk
257 ant that samples be collected and stored for pharmacogenetic study in future clinical trials.
258 We conducted a multicenter observational and pharmacogenetic study of 200 patients with DLE treated w
259 mine treatment in a prospective double-blind pharmacogenetics study in first-generation Mexican Ameri
260 ed by Genetic Haplotype Markers) study was a pharmacogenetics study of statin efficacy and safety.
261   This is the largest and most comprehensive pharmacogenetics study to date examining clinical respon
262           Design, Setting, and Participants: Pharmacogenetic substudy of 1545 patients who participat
263 ity to HIT, but it is likely that additional pharmacogenetic susceptibility factors will be discovere
264  intracellular signaling, as well as through pharmacogenetic targeting.
265 encephalogram (EEG) power spectrum using the pharmacogenetic technique, the 'designer receptors exclu
266                                 Here we used pharmacogenetic techniques to show a causal relation bet
267                                              Pharmacogenetic techniques used on tumour and host tissu
268 s to feeding behaviour using optogenetic and pharmacogenetic techniques.
269 ghlight which variants and in which contexts pharmacogenetic testing can be implemented by practicing
270                                              Pharmacogenetic testing combined with monitoring of hair
271 ng may be beneficial, the data today support pharmacogenetic testing for certain variants on an indiv
272                                 In contrast, pharmacogenetic testing for HLA-B*1502 before carbamazep
273           One blood sample was collected for pharmacogenetic testing from each patient who elected to
274 lso presents the current recommendations for pharmacogenetic testing in clinical practice and explore
275 ical trials will determine if routine use of pharmacogenetic testing may be beneficial, the data toda
276 tes that they stand to benefit the most from pharmacogenetic testing.
277 abeling in 2007 to suggest, but not mandate, pharmacogenetic testing.
278 ves for translating clopidogrel and warfarin pharmacogenetic tests to clinical practice.
279                                              Pharmacogenetics, though presently confined to the asses
280 search into the role of pharmacokinetics and pharmacogenetics to guide appropriate dosing of obese pa
281  extension of previous studies of naltrexone pharmacogenetics to individuals of Asian descent, an eth
282 ngs, two-photon microscopy, optogenetics and pharmacogenetics to show how repeated cocaine exposure a
283 olecular genetics along with optogenetic and pharmacogenetic tools for perturbing neuron function hav
284                                 Anatomic and pharmacogenetic tools were used to identify the pathways
285 etically encoded anatomical, optogenetic and pharmacogenetic tools, we demonstrate that activation of
286 ls represent a promising novel target in the pharmacogenetic treatment of alcohol and drug addiction.
287 ogy of the disease could help development of pharmacogenetic treatments.
288 ) project, a partially randomized open-label pharmacogenetic trial.
289 vergent findings reported by recent warfarin pharmacogenetic trials.
290 examine the association between clinical and pharmacogenetic variables and statin concentrations in p
291 ative or opiate doses and pharmacokinetic or pharmacogenetic variables, such as drug plasma levels (e
292 ne uncertain variants in cancer genes (98%), pharmacogenetic variants (89%), and recessive carrier mu
293 to review the association data for the major pharmacogenetic variants associated with commonly used c
294 nificant racial differences in prevalence of pharmacogenetic variants were observed, although small s
295  perturbation enables identification of true pharmacogenetic variants.
296 is table may potentially increase the use of pharmacogenetic warfarin dosing in clinical practice; ho
297 gly popular, predominantly in the context of pharmacogenetics, where the survival endpoint could be d
298                                  Ultimately, pharmacogenetics will give providers the options for imp
299                           Future utility for pharmacogenetics will wax or wane depending on the natur
300 Optogenetics with microbial opsin genes, and pharmacogenetics with designer receptors, represent pote

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