kwic
effects+of
effects+of
right
off
ON
31
1
100
500
strict
ELIZA cgi-bash version rev. 1.91
- Medical English LInking keywords finder for the PubMed Zipped Archive (ELIZA) -
return
kwic search for effects of out of >500 occurrences
291610 occurrences (No.83 in the rank) during 5 years in the PubMed. [cache]
--- ABSTRACT ---
--- ABSTRACT END ---
[frequency of next (right) word to effects of]
291610 occurrences (No.83 in the rank) during 5 years in the PubMed. [cache]
| 31) Thus, our results further support the role of ATP2C2 locus in language-related phenotypes and pinpoint the possible effects of a specific rare variant at molecular level. |
| PMID:33864365 DOI:10.1093/hmg/ddab111 |
| 2021 Human molecular genetics |
| * A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures. |
| - At least 5% of children present unexpected difficulties in expressing and understanding spoken language. This condition is highly heritable and often co-occurs with other neurodevelopmental disorders such as dyslexia and ADHD. Through an exome sequencing analysis, we identified a rare missense variant (chr16:84405221, GRCh38.p12) in the ATP2C2 gene. ATP2C2 was implicated in language disorders by linkage and association studies, and exactly the same variant was reported previously in a different exome sequencing study for language impairment (LI). We followed up this finding by genotyping the mutation in cohorts selected for LI and comorbid disorders. We found that the variant had a higher frequency in LI cases (1.8%, N = 360) compared with cohorts selected for dyslexia (0.8%, N = 520) and ADHD (0.7%, N = 150), which presented frequencies comparable to reference databases (0.9%, N = 24 046 gnomAD controls). Additionally, we observed that carriers of the rare variant identified from a general population cohort (N = 42, ALSPAC cohort) presented, as a group, lower scores on a range of reading and language-related measures compared to controls (N = 1825; minimum P = 0.002 for non-word reading). ATP2C2 encodes for an ATPase (SPCA2) that transports calcium and manganese ions into the Golgi lumen. Our functional characterization suggested that the rare variant influences the ATPase activity of SPCA2. Thus, our results further support the role of ATP2C2 locus in language-related phenotypes and pinpoint the possible effects of a specific rare variant at molecular level. |
[
right
kwic]
(1)26  the |
(19)3 exposure |
(37)2 blast |
(55)2 low-intensity |
| (2)7 a |
(20)3 microplastics |
(38)2 both |
(56)2 marijuana |
| (3)7 different |
(21)3 mutations |
(39)2 bushfire |
(57)2 medical |
| (4)7 these |
(22)3 neonatal |
(40)2 camel |
(58)2 metabolic |
| (5)6 alcohol |
(23)3 separation |
(41)2 chronic |
(59)2 mitochondrial |
| (6)6 physical |
(24)3 spatial |
(42)2 dietary |
(60)2 nelfinavir |
| (7)5 an |
(25)2 BBR |
(43)2 donepezil |
(61)2 noise |
| (8)5 chemotherapy |
(26)2 CTS |
(44)2 early |
(62)2 person-centered |
| (9)4 Caps |
(27)2 EPEs |
(45)2 estrogen |
(63)2 resistance |
| (10)4 school |
(28)2 FGF21 |
(46)2 flaps |
(64)2 severe |
| (11)4 two |
(29)2 IGF-1 |
(47)2 foam |
(65)2 sleep |
| (12)3 AKR1C1 |
(30)2 IMT |
(48)2 gene |
(66)2 social |
| (13)3 Ang |
(31)2 METTL3 |
(49)2 genetic |
(67)2 sorafenib |
| (14)3 COVID-19 |
(32)2 Malathion |
(50)2 high |
(68)2 three |
| (15)3 OIT |
(33)2 RT |
(51)2 high-dose |
(69)2 treatment |
| (16)3 acute |
(34)2 Rap |
(52)2 insulin |
|
| (17)3 each |
(35)2 adropin |
(53)2 lactate |
|
| (18)3 exercise |
(36)2 aging |
(54)2 local |
add keyword
--- WordNet output for effects ---