Medial prefrontal cortex neurons integrate amygdala and hypothalamic oxytocin signals to mediate stress-induced social alterations.
The 1 match
- [1] § Material and methods › In vivo microendoscopic calcium imaging › Principal component analysis ↔ Functions_PCA.py, lines 549–585 · score 0.61 · Explained variance ratioes, PCs, component, PCA, behaviours
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The authors' code
Python · 662 lines · 20 KB · no license · 1 match
- # Functions.py
- #
- # Author: Xiaoqian Sun, Apr 2023
- #
- # Functions for projection project
- from IPython.core.debugger import set_trace
- # Import Packages
- #========================================================================================
- import os
- import cv2
- import math
- import itertools
- import scipy as sp
- import numpy as np
- import pandas as pd
- from PIL import Image
- import seaborn as sns
- import tifffile as tiff
- import matplotlib as mpl
- from itertools import groupby
- from operator import itemgetter
- import matplotlib.pyplot as plt
- from scipy.stats import pearsonr
- import matplotlib.colors as mcolors
- from sklearn.decomposition import PCA
- # from oasis.functions import deconvolve
- from sklearn.preprocessing import MinMaxScaler
- from scipy.ndimage.filters import gaussian_filter
- from sklearn.ensemble import RandomForestClassifier
- from sklearn.model_selection import train_test_split
- from scipy.signal import chirp, find_peaks, peak_widths
- import warnings
- warnings.filterwarnings('ignore')
- # Functions
- #========================================================================================
- def process_frame(df):
- '''
- Aim:
- frame 0 at trace file may not sart from time 0
- called in function `add_event_label()`
- '''
- # get frame list
- frame_list = df.index.values.tolist()
- # get starting value
- a = frame_list[0]
- new_frame_list = [(i-a) for i in frame_list]
- return(new_frame_list)
- def process_event_interval(df):
- '''
- Aim:
- time in event file doesn't always start from 0s, fix that
- called in function `add_event_label()`
- '''
- new_col = []
- for col in df.columns.tolist():
- new_col.append(col.strip())
- df.columns = new_col
- event_list = df[['From Second','To Second']].values.tolist()
- startTime = df['From Second'].values.tolist()[0]
- new_event_list = []
- for event in event_list:
- new_event = [x -startTime for x in event]
- new_event_list.append(new_event)
- return(new_event_list)
- # +
- def get_event_label(event_df):
- '''
- Aim:
- for OFT
- translate 'event' in eventFile to integer label
- each row (corresponding to each time interval) of event is assigned a label
- called in function `add_event_label()`
- '''
- # get event status list
- Event_status = event_df['Event'].values.tolist()
- # compact event label list for three sessions
- event_label = []
- # ['In_all',
- # 'In_right',
- # 'Investigating_RIGHT_SNIFF',
- # 'In_left',
- # 'Investigating_LEFT_SNIFF']
- # if which_status_to_check_frame == 'Investigating_RIGHT_SNIFF':
- # which_status_to_check_frame = str(11)
- # elif which_status_to_check_frame == 'Investigating_LEFT_SNIFF':
- # which_status_to_check_frame = str(12)
- # elif which_status_to_check_frame == 'In_right':
- # which_status_to_check_frame = str(21)
- # elif which_status_to_check_frame == 'In_all':
- # which_status_to_check_frame = str(22)
- # elif which_status_to_check_frame == 'In_left':
- # which_status_to_check_frame = str(23)
- # else:
- for i in Event_status:
- if i.strip() == 'In_right':
- event_label.append(21)
- elif i.strip() == 'Investigating_RIGHT_SNIFF' :
- event_label.append(11)
- elif i.strip() == 'In_left':
- event_label.append(23)
- elif i.strip() == 'Investigating_LEFT_SNIFF':
- event_label.append(12)
- else:
- event_label.append(22)
- # for i in Event_status:
- # if i.strip() == 'Area:Mouse 1 Center In floor':
- # event_label.append(10)
- # elif i.strip() == 'Area:Mouse 1 Center In All ' :
- # event_label.append(10)
- # elif i.strip() == 'Area:Mouse 1 Center In central area':
- # event_label.append(11)
- # elif i.strip() == 'Area:Mouse 1 Center In corner':
- # event_label.append(12)
- # elif i.strip() == 'Mouse 1 sniffing On wall':
- # event_label.append(30)
- # elif i.strip() == 'Mouse 1 Grooming in Area All':
- # event_label.append(31)
- # elif i.strip() == 'Mouse 1 Grooming in Area floor':
- # event_label.append(31)
- # elif i.strip() == 'Mouse 1 Locomotion in Area All':
- # event_label.append(32)
- # else:
- # event_label.append(90)
- return(event_label)
- # -
- def add_event_label(trace_df, event_path):
- '''
- Aim:
- add event_label to each frame
- one frame can have several label (since mouse can in a location and do something)
- Retrun:
- trace dataframe with one label column
- '''
- frame_list = process_frame(trace_df)
- #get event dataframe/eventIntervals/eventLabel
- # event_df = pd.read_csv(event_path)
- event_df = pd.read_excel(event_path)
- interval_list = process_event_interval(event_df)
- event_label = get_event_label(event_df)
- # add label to each frame
- frame_label_list = []
- for frame in frame_list:
- frame_label = str()
- for i in range(len(interval_list)): # one frame can be in several interval
- if min(interval_list[i]) <= frame <= max(interval_list[i]) :
- frame_label = frame_label+ str(event_label[i])
- # convert str to int
- if len(frame_label) == 0:
- frame_label = np.nan
- else:
- frame_label = int(frame_label)
- # append frame label to list
- frame_label_list.append(frame_label)
- # add label list to trace df
- new_df = trace_df.copy()
- new_df['Frame_Label'] = frame_label_list
- new_df = new_df.dropna()
- return(new_df)
- def find_compositeIntervals(df,
- which_status_to_check,
- intervalLength=20,
- if_CombineAdjacentChunks=True,
- gapMax=10):
- '''
- Aim:
- a mouse might get into a location/behavior several time during a whole session. this function is to
- find all intervals that the mouse gets into certain state.
- Arguments:
- - df: neuron activity df with status label for each frame (1-in state)
- - which_status_to_check: behavior/location (choose from center/corner/sniffing/grooming)
- - intervalLength: minimum size of state-interval, that is the interval must longer than #_frames, otherwise, this interval will be dumped
- - if_CombineAdjacentChunks: if merge 2 neighbours
- - gapMax: if gap between two chunks less than gapMax, merge the two
- Return:
- - kept chunks, sublists in list
- '''
- df_status = check_frame_interval(df, which_status_to_check, ifKeep=True)
- # get status list
- status_list = df_status['status'].values.tolist()
- # get 1 index
- index_1_list = [i for i, x in enumerate(status_list) if x == 1]
- # pick all consecutive chunks
- chunks = []
- try:
- for k, g in groupby(enumerate(index_1_list), lambda ix:ix[0]-ix[1]):
- chunk = list((map(itemgetter(1), g)))
- chunks.append([chunk[0], chunk[-1]])
- # combine small chunks
- if if_CombineAdjacentChunks:
- combinedchunks = []
- combinedchunks.append(chunks[0]) # initialize with first chunk
- #print('starting point', combinedchunks)
- combinedIndex = 0
- for chunkIndex in range(1, len(chunks)):
- chunkPre = combinedchunks[combinedIndex]
- chunkLat = chunks[chunkIndex]
- #print('1st round, pre:',chunkPre, ' lat:',chunkLat, ', diff=', chunkLat[0]-chunkPre[1] )
- if chunkLat[0]-chunkPre[1] <= gapMax:
- del combinedchunks[combinedIndex]
- #print('after del 0,', combinedchunks)
- combinedchunk = chunkPre+chunkLat
- #print('combined chunk is', combinedchunk)
- combinedchunks.append([combinedchunk[0], combinedchunk[-1]])
- else:
- combinedchunks.append(chunkLat)
- combinedIndex = combinedIndex + 1
- else:
- combinedchunks = chunks
- # remove small chunks
- keep_combinedchunks = []
- for chunk in combinedchunks:
- if chunk[1]-chunk[0] >= intervalLength:
- keep_combinedchunks.append(chunk)
- except Exception as e:
- keep_combinedchunks = chunks
- print(' ', e)
- return (keep_combinedchunks)
- def normBA(df,df_B_list,df_A_list,beforeB=False,baseSecond=2):
- '''
- Aim:
- normalize trace based on some frames before/start of the trace
- Arguments:
- - df: trace df
- - df_B_list: dataframe list BEFORE behavior/location onset
- - df_A_list: dataframe list AFTER behavior/location onset
- - beforeB: if use a period before df_B to calculate baseline.
- If True, than use baseSecond before de_B to calculate baselinse, otherwise use the entire df_B as baseline
- - baseSecond: how long before df_B are used to calculate baseline
- Return:
- - normalized df_B_list and df_A_list
- '''
- df_BN_list = []; df_AN_list = []
- if len(df_B_list)!=0 and len(df_A_list) !=0:
- for dfIndex in range(len(df_B_list)):
- dfB = df_B_list[dfIndex]
- dfA = df_A_list[dfIndex]
- # find baseline
- if beforeB:
- dfBM = df.loc[(dfB.index[0]-baseSecond):dfB.index[0]]
- else:
- dfBM = dfB.copy()
- dfBM.loc['mean'] = dfBM.mean(axis=0)
- # norm first/second half based on baseline
- dfBN = dfB-dfBM.loc['mean']
- dfAN = dfA-dfBM.loc['mean']
- df_BN_list.append(dfBN)
- df_AN_list.append(dfAN)
- return (df_BN_list, df_AN_list)
- def get_BonsetA(df,
- which_status_to_check,
- fps,
- secForward=10,
- secBackward=10,
- beforeB=False,baseSecond=2,intervalLength=20,if_CombineAdjacentChunks=True,gapMax=10,ifNorm=True):
- '''
- Aim:
- Through function find_compositeIntervals() we locate interval that mouse was in certain state.
- By calling this function, we enlarge each interval forward #secForward seconds and make it last #secBackward seconds
- For example (1 interval C), C=[second_10, second_25] or C=[second_10, second_15].
- By calling this function, we make C=[second_8, second_20]
- Arguments:
- df: dff
- which_status_to_check: the behavior of onset
- secForward: seconds to enlarge forward from onset
- secBackward: seconds to include backward from onset
- other arguments are either from function find_compositeIntervals() or normBA(), check there for more details
- '''
- df_status = check_frame_interval(df, which_status_to_check, ifKeep=True)
- combinedchunks = find_compositeIntervals(df,which_status_to_check,intervalLength=intervalLength,
- if_CombineAdjacentChunks=if_CombineAdjacentChunks,gapMax=gapMax)
- df_Bonset_list = []
- df_onsetA_list = []
- if len(combinedchunks) > 0:
- # enlargy each interval 100 frames (50 forward, 50 afterward)
- for interval in combinedchunks:
- if interval[0] >= secForward*fps:
- Bonset_start = interval[0] - secForward*fps
- Bonset_end = interval[0]
- onsetA_start = interval[0]
- if interval[0] + secBackward*fps < len(df):
- onsetA_end = interval[0] + secBackward*fps
- #----------------locate----------------#
- Bonset_df = df_status.iloc[Bonset_start:Bonset_end]
- Bonset_df = Bonset_df.drop('status', axis = 1)
- df_Bonset_list.append(Bonset_df)
- onsetA_df = df_status.iloc[onsetA_start:onsetA_end]
- onsetA_df = onsetA_df.drop('status', axis = 1)
- df_onsetA_list.append(onsetA_df)
- # norm
- if ifNorm:
- df_Bonset_listN, df_onsetA_listN = normBA(df_status,df_Bonset_list,df_onsetA_list,beforeB=beforeB,baseSecond=baseSecond)
- else:
- df_Bonset_listN, df_onsetA_listN = df_Bonset_list,df_onsetA_list
- return (df_Bonset_listN, df_onsetA_listN)
- def check_frame_interval(df, which_status_to_check_frame, ifKeep=True):
- # set_trace()
- # set up which_status_to_check_frame
- if which_status_to_check_frame == 'Investigating_RIGHT_SNIFF':
- which_status_to_check_frame = str(11)
- elif which_status_to_check_frame == 'Investigating_LEFT_SNIFF':
- which_status_to_check_frame = str(12)
- elif which_status_to_check_frame == 'In_right':
- which_status_to_check_frame = str(21)
- elif which_status_to_check_frame == 'In_all':
- which_status_to_check_frame = str(22)
- elif which_status_to_check_frame == 'In_left':
- which_status_to_check_frame = str(23)
- else:
- raise ValueError('Not approved status. choose from: Investigating_RIGHT_SNIFF, Investigating_LEFT_SNIFF, In_right, In_all, In_left')
- #df = add_event_label(df, event_1_path, event_2_path, event_3_path, mice_path)[which_session]
- frame_label_list = df['Frame_Label'].values.tolist()
- # to separate status label, eg:20214111
- n = 2
- check_frame_label_list = []
- for line in frame_label_list:
- line = str(line)
- line_list= [line[i:i+n] for i in range(0, len(line), n)]
- if which_status_to_check_frame in line_list:
- check_frame_label_list.append(1)
- else:
- check_frame_label_list.append(0)
- df['status'] = check_frame_label_list
- df_keep = df[ (df['status'] == 1)]
- # df_keep = df_keep.drop('status', axis = 1)
- # df_keep = df_keep.drop('Frame_Label', axis = 1)
- print('the shape of the dataframe in the status is:', df_keep.shape)
- return(df_keep)
- # +
- def average_nActEntries(df_list,neuron_list,fps,seconds):
- '''
- Aim:
- get average activity around onset for each neuron across entries
- Return:
- a dataframe with all mean activity of each neuron [num_frames, num_neurons]
- '''
- frames = seconds*fps
- avgNeuron_actEntries = pd.DataFrame()
- if len(df_list) > 0:
- for nCol in neuron_list:
- # get mean activity of this neuron across entries]
- nAct_entries = []
- for i in range(len(df_list)):
- if df_list[i].shape[0] == frames:
- # nAct_entries.append(df_list[i][nCol])
- nAct_entries.append(df_list[i][nCol].astype(float))
- # set_trace()
- nAct_mean = np.mean(np.array(nAct_entries), axis=0)
- avgNeuron_actEntries[nCol] = nAct_mean
- return(avgNeuron_actEntries)
- # -
- def filterOut_nonceONce(df, fps, secF):
- '''
- remove neurons that not showing ceON neurons around center
- specificly designed for 3-AverageTrace_4ONs_heatmap
- '''
- df_keep = df.copy()
- f, n = df.shape
- for i in range(n):
- act = df.iloc[:, i]
- Bavg = np.mean(act[:fps*secF])
- avgA = np.mean(act[fps*secF:fps*secF*3])
- if avgA<Bavg:
- df_keep = df_keep.drop(df.columns[i], axis=1)
- return(df_keep)
- def filterOut_nonceONco(df, fps, secF):
- '''
- remove neurons that not showing ceON neurons around corner (drop onset)
- specificly designed for 3-AverageTrace_4ONs_heatmap
- '''
- df_keep = df.copy()
- f, n = df.shape
- for i in range(n):
- act = df.iloc[:, i]
- Bavg = np.mean(act[:fps*secF])
- avgA = np.mean(act[fps*secF:fps*secF*3])
- if avgA>Bavg:
- df_keep = df_keep.drop(df.columns[i], axis=1)
- return(df_keep)
- def get_overlap(lists):
- ls=[set(l) for l in lists]
- fst=ls[0]
- for l in ls[1:]:
- fst.intersection_update(l)
- return (len(fst), fst)
- def fit_apply_PCA(input_df_Std, ifPrint=True):
- '''
- Aim:
- apply PCA
- '''
- pcaModel = PCA(n_components=4)
- input_Reduced_Std = pcaModel.fit_transform(input_df_Std)
- if ifPrint:
- print('first 3PCs explain', round(sum((pcaModel.explained_variance_ratio_[0:3])),3), \
- 'PC1='+str(round(pcaModel.explained_variance_ratio_[0],3))+\
- ' PC2='+str(round(pcaModel.explained_variance_ratio_[1],3))+\
- ' PC3='+str(round(pcaModel.explained_variance_ratio_[2],3)))
- #print('explained_variance_ratio_', pcaModel.explained_variance_ratio_)
- # reduced df
- input_Reduced_df = pd.DataFrame(input_Reduced_Std)
- input_Reduced_df.columns = ['PC1', 'PC2', 'PC3', 'PC4']
- return(input_Reduced_df, pcaModel)
- def generate_PCA_summaryDF(reduced_df, pcaModel, behaviorList, mouseName):
- '''
- Aim:
- generate PCA summary, 4 PCs
- eigenvector=features, eigenvalues=coefficient, mean=X.mean
- also generate df for running log, just explained variance ratio
- '''
- # PC summary
- #----------------------------------------------------
- dic_eigen = {'Eigenvector 1':pcaModel.components_[0],
- 'Eigenvector 2':pcaModel.components_[1],
- 'Eigenvector 3':pcaModel.components_[2],
- 'Eigenvector 4':pcaModel.components_[3],
- 'Sample Mean':pcaModel.mean_,
- 'Eigenvalues':pcaModel.explained_variance_,
- 'Explained Ratio':pcaModel.explained_variance_ratio_,
- 'singular Values':pcaModel.singular_values_,
- 'behavior':behaviorList}
- dic_eigen = dict([(k,pd.Series(v)) for k,v in dic_eigen.items() ])
- df_eigen = pd.DataFrame(dic_eigen)
- # concat PCs
- PCA_summary = pd.concat([df_eigen, reduced_df], axis=1)
- # running Log
- #----------------------------------------------------
- runningLog = pcaModel.explained_variance_ratio_
- runningLog_dic = {'mouseName':mouseName,
- 'first_3PCs': sum(runningLog),
- 'PC1':runningLog[0],
- 'PC2': runningLog[1],
- 'PC3':runningLog[2]}
- runningLog_dic = dict([(k,pd.Series(v)) for k,v in runningLog_dic.items() ])
- runningLog_df = pd.DataFrame(runningLog_dic)
- return(PCA_summary, runningLog_df)
- # Plot
- # ========================================================================================
- def plot_3D_4Behaviors(PCA_df,behaviors=['center', 'corner', 'sniffing', 'grooming'],cs=['r','g','b','black'],
- alphas=[0.6, 0.1, 0.8, 1], ifSave=True,savePath=None,filename=None):
- '''
- Aim:
- plot single 3D line plot and save
- different behavior, differetn scatter plot
- '''
- fig = plt.figure(figsize=(10,10))
- ax = fig.add_subplot(111, projection='3d')
- for bIndex in range(len(behaviors)):
- b = behaviors[bIndex]
- x = PCA_df[PCA_df['behavior']==b]['PC1']
- y = PCA_df[PCA_df['behavior']==b]['PC2']
- z = PCA_df[PCA_df['behavior']==b]['PC3']
- ax.scatter(x, y, z, c=cs[bIndex], marker='o', alpha=alphas[bIndex], label=b)
- plt.legend()
- if ifSave:
- if not os.path.exists(savePath):
- os.makedirs(savePath)
- plt.savefig(os.path.join(savePath, filename), dpi=300)
- plt.close()
- else:
- plt.show()
- def plot_2D_4Behaviors(PCA_df,
- behaviors=['center', 'corner', 'sniffing', 'grooming'],
- cs=['r','g','b','black'],
- alphas=[0.6, 0.1, 0.8, 1],
- ifSave=True,savePath=None,filename=None):
- '''
- Aim:
- plot single 3D line plot and save
- different behavior, differetn scatter plot
- '''
- fig = plt.figure(figsize=(10, 10))
- for bIndex in range(len(behaviors)):
- b = behaviors[bIndex]
- x = PCA_df[PCA_df['behavior']==b]['PC1']
- y = PCA_df[PCA_df['behavior']==b]['PC2']
- plt.scatter(x, y, marker='o', color=cs[bIndex], alpha=alphas[bIndex], label=b)
- plt.legend()
- if ifSave:
- if not os.path.exists(savePath):
- os.makedirs(savePath)
- plt.savefig(os.path.join(savePath, filename), dpi=300)
- plt.close()
- else:
- plt.show()
Functions_PCA.py at commit 4e3dd13, no license · at the source
Overview
- School of Clinical and Basic Medical Sciences, Shandong First Medical University,Jinan, China
- School of Public Health, Shandong First Medical University,Jinan, China
- College of Dentistry, Shandong First Medical University,Jinan, China
- Jinan Maternity and Child Care Hospital Affiliated to Shandong First Medical University,Jinan, China
- School of Public Health, Jining Medical University,Jining, China
Abstract
The abstract is not reproduced here: the paper's license (CC BY-NC-ND) does not allow it. Read it in the paper, at the publisher or on Europe PMC.
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Xulab-SDFMU/mPFC_circuits_Stress_Social
4e3dd1392abb925ec135fc911b8f023680e37e40, 1 August 2025Availability: 1 check, the latest on 29 September 2026: the link answers
- 29 September 2026: the link answers
8 files
- FWHM.ipynb, Jupyter, 1,201 lines
- Functions_PCA.py, Python, 662 lines, 1 match
- Neuron_Sample_Trace.ipyn
b , Jupyter, 839 lines - PCA_raletive_distance.ip
ynb , Jupyter, 269 lines - Transienttrate_Amplitude
.ipynb , Jupyter, 1,036 lines - convert_social_raw_data.
ipynb , Jupyter, 97 lines - merge_behavior_epochs.ip
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mPFC_circuits_Stress_Soc ial
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Data
Datasets cited
- figshare:30084418, at figshare; found in “Data availability”
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Recorded: type, language, journal, volume, issue, pages, dates, 10 authors, 3 keywords, 13 MeSH terms, 2 funders, 60 references.
Cite
This paper
Zhang, Y., Zhang, Z.-Q., Zhai, Z.-J., Ren, X., Zuo, S., Ma, Z., Liu, M., Li, D., Wang, Y., & Xu, P. (2026). Medial prefrontal cortex neurons integrate amygdala and hypothalamic oxytocin signals to mediate stress-induced social alterations. Communications biology, 9(1), 870. https://
BibTeX
@article{zhang2026medial
author = {Zhang, Yujing and Zhang, Zi-Qi and Zhai, Zi-Jie and Ren, Xuchao and Zuo, Siyi and Ma, Zheng and Liu, Min and Li, Dong and Wang, Yue and Xu, Pan},
title = {{Medial prefrontal cortex neurons integrate amygdala and hypothalamic oxytocin signals to mediate stress-induced social alterations}},
journal = {Communications biology},
year = {2026},
month = apr,
volume = {9},
number = {1},
pages = {870},
publisher = {Nature Publishing Group},
issn = {2399-3642},
doi = {10.1038/
url = {https://
pmid = {42026195},
pmcid = {PMC13316100}
}
RIS
TY - JOUR
AU - Zhang, Yujing
AU - Zhang, Zi-Qi
AU - Zhai, Zi-Jie
AU - Ren, Xuchao
AU - Zuo, Siyi
AU - Ma, Zheng
AU - Liu, Min
AU - Li, Dong
AU - Wang, Yue
AU - Xu, Pan
TI - Medial prefrontal cortex neurons integrate amygdala and hypothalamic oxytocin signals to mediate stress-induced social alterations
T2 - Communications biology
J2 - Commun Biol
PY - 2026
DA - 2026/
VL - 9
IS - 1
SP - 870
SN - 2399-3642
PB - Nature Publishing Group
DO - 10.1038/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.1038/
"type": "article-journal",
"title": "Medial prefrontal cortex neurons integrate amygdala and hypothalamic oxytocin signals to mediate stress-induced social alterations",
"container-title": "Communications biology",
"author": [
{
"family": "Zhang",
"given": "Yujing"
},
{
"family": "Zhang",
"given": "Zi-Qi"
},
{
"family": "Zhai",
"given": "Zi-Jie"
},
{
"family": "Ren",
"given": "Xuchao"
},
{
"family": "Zuo",
"given": "Siyi"
},
{
"family": "Ma",
"given": "Zheng"
},
{
"family": "Liu",
"given": "Min"
},
{
"family": "Li",
"given": "Dong"
},
{
"family": "Wang",
"given": "Yue"
},
{
"family": "Xu",
"given": "Pan"
}
],
"container-title-short":
"volume": "9",
"issue": "1",
"page": "870",
"DOI": "10.1038/
"PMID": "42026195",
"PMCID": "PMC13316100",
"ISSN": "2399-3642",
"publisher": "Nature Publishing Group",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
4,
23
]
]
}
}
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