The CHRISTMAS, the 'Cys-His-Arg-Ile-Ser-Thr' (C-H-R-I-S-T) amino acid sequence and the SARS-CoV-2 Spike.

Merry Christmas to everyone, also to those who celebrate, enjoy, believe and remember traditions. This post was written on December 24-th, the Christmas Eve, the day of the year, many believe, including myself, Jesus was born.

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Updates:

4/16/2025: The content of this post is directly connected with this post titled “ERASING CHRIST THE QUIET REMOVAL OF JESUS FROM OUR TIMELINE“ by Ron:

ERASING CHRIST THE QUIET REMOVAL OF JESUS FROM OUR TIMELINE

12/25/2023 The bioinformatics analysis presented here will be continued, so checking occasionally for those who are interested would make sense. The post might become huge… Thank you for reading and not-unsubscribing;))

1/1/2024: HAPPY NEW YEAR WITH NEW HOPES for more JUSTICE, PEACE and LOVE and appreciation for our Creator, on this planet. An incredible scientist will REVOLUTIONIZE the world with new truths, FACTS: https://expose-news.com/2024/01/01/let-a-scientist-speak-presentation-goes-viral-because-its-true/ and music, can support our battled souls on a different level:

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There is only one word which relates to the night today and that is the word CHRIST.

It means a lot to many, special birth, love, wonders, devotion, forgiveness, peace, special death, but also the highest power.

This short post will relate molecular biology and religion, via this one word CHRIST. For people who read bible the meaning of WORD is very important. In todays world where religion is attacked on every level, where values are destroyed, and creation is being overwritten via GENETICS, one has to realize the level of hidden complexity by those who have the power to know and to decide what others know, and become. As usual, all will be based on bioinformatics, assumed as a known tool for the reader.

Natural proteins contain 20 amino acids described by a single letter code covering the entire alphabet except for the letters : B, J, O, U, Z, X. These missing letters in protein codes already exclude the existence of the short pentapeptide, like for example ‘J-E-S-U-S’. As a side note, there is one special artificial amino acid ‘hybrid’ called glyphosate. It represents a mix of glycine (the human inhibiting neurotransmitter) and a phosphono-group, together called N-phosphonomethylglycine. Wi-ki calls it broad-spectrum systemic herbicide and crop desiccant… And there are more, but will be left out for now.

One can start with opening the NIH BLAST page at https://blast.ncbi.nlm.nih.gov/Blast.cg (with ‘PROTEIN’ analysis option) and type into the search window the fasta code ‘CHRIST’ which is equivalent to ‘Cys-His-Arg-Ile-Ser-Thr’=’Cysteine-Histidine-aRginine-Isoleucine-Serine-Threonine’ or the string of letters ‘C-H-R-I-S-T’. Now search for ‘Reference Proteins’ with blastp algorithm and just hit BLAST button. Enough to choose the default first 100 hits, one can go much higher and deepen the analysis.

If the amino acid sequence ‘CHRIST’ (from now on it will be called ‘CHRIST section’ because in this search it represents a short peptide as defined by molecular biologists, an amino acid sequence) had no meaning in all the found proteins, their relation for example to SARS-CoV-2 Spike (its amino acid sequence is at https://www.ncbi.nlm.nih.gov/protein/YP_009724390.1) should be zero, but it is not.

The result shows proteins with 100% hit for the word ‘CHRIST’ from all possible organisms sorted after amino acids length, i.e. molecular weight. Let’s take the first one, non-ribosomal peptide synthetase with the NIH code WP_052438536.1, and compare it with the SARS-CoV-2 Spike (BLAST search with 2 entries in which Spike will be the line with query in all the examples below), one gets 78% coverage with 47% identities, using special parameters. Here just 3 hits, chosen according their importance in Spike features, among countless others:

Query  663   DIPIGAGICASYQTQTNSPRRAR  685 Spike's FURIN Site
             + P  AG+ A  ++ T + ++AR
Sbjct  6346  EAPTVAGVAARIESLTTTKKKAR  6368  WP_052438536.1
Query  460   NLKPFERDISTEIYQAGST  478 Spike's ACE2 binding site
             +L P  RD+S+  Y A +T
Sbjct  3323  SLAPLARDVSAA-YAARTT  3340 WP_052438536.1
Query  704   TMSLGAENSVAYSNNSIAIPTNFTISVTTEILPVSMTKTSVDCTMYICGDST  747
               +     S  +++ ++ +P+    +   E+     ++T  D T  + GD T
Sbjct  2581  DVAECHRISTEWNDTAVDLPA----ATLPELFAAQAARTP-DATALVFGDET  2619

Note the last line with the CHRIST sequence, Spike doesn’t have it. Let’s take the IgGFc-binding protein XP_030268704.1, which comes up for many organisms in this search. The first is the section containing the ‘ALLAG-TITS-G-WTF-GAGAA‘, it was mentioned many times in my posts, here it really looks like it was added into Spike with the conserved ‘TSGW’ tetrapeptide… Spike sequence is in query line, IgGFc sequence in Sbjct line:

Query  844  IAARDLICAQKFNG-LTVLPPLLTDEMIAQYTSALLAGTITSGWTFGAGAALQIPFAMQM  
            + ++D   A   NG L+ LP +L +  I  Y         TSGW     A ++  F +++
Sbjct  409  VISKDNPGAVVINGELSNLPMMLNNNTIHLY---------TSGWF----AVIETDFGVKL 
Query 1034  LGQSKRVDFCGKGYHLMSFPQSAPHGVVFLHVTYVPAQEKNFTTAPAICHDGKAHFPREG 
            +GQS   D C    H  S  Q A   VV  ++T  P +          C+  +      G
Sbjct  1067 VGQSIITDDC----HRISTCQ-ASGVVVSQNMTCDPNESCLVKNGVMGCYIQQCFLDSNG

The last line with the divided CHRIST sequence is not present in Spike, except for the C, H and S residues. Is IgG-Fc somewhat related with covid19? Just one citation^1 showing how important it is, with no further analysis. The next one, transmembrane channel-like protein 3 XP_049638825.1, with over 30% identities:

Query  1    MFVFLVLLPLVSSQCVNLTTRTQLPPAYTNS  31 Spike 
            M  F+V+  L++ Q    T+R ++PP +  S
Sbjct  154  MGAFVVIPELIAGQPFGSTARKRVPPEHVAS  184  XP_049638825.1

Query  1082  CHDGKAHFPREGVFVSNGTH  1101 Spike 
             CH   +  P+     +  TH
Sbjct  746   CHRISTCSPKGRCSRAPSTH  765 XP_049638825.1

The word ‘CHRIST’ disappears in Spike, except for the first CH and last T residues. despite of many similar sections. Try to run similarities with the transmembrane channel-like protein 3 and nsp3 from SARS-CoV-2, 67% sequence coverage and ~40% identities including section showing their direct electrostatic relationship:

Query  842  EEEGEEE  848 
            EEE EE+
Sbjct  154  EEEQEED  160

Next protein, XP_007803561.1, P-type cation-transporting ATPase, this time the ‘CHRIST’ section in the first hit is not conserved, but other fragments are, the special perverse one, even for this totally different protein, comes up, again:

Query  91   YFASTEKSNIIRGWIFGTTLDSK  113 Spike2020
            Y A T      R    G +LD +
Sbjct  141  YIAKTTGFTCHRISTHGQSLDIR  163 XP_007803561.1
Query  880  GTITSG-------------WTFGAGAALQI------PFAMQMAYRFNGIGVTQNVLYENQ  
            GT+T G              +  A  AL +      P +  +A      GV + VL EN 
Sbjct  581  GTLTKGELSVLAEDHFSESQSVAASIALGLTMNSKHPVSAALAAHLQARGV-EPVLIENM  

Cation transporting ATP-ase is involved in binding Mg, a process affected by SARS-CoV-2^2.

Next protein eukaryotic translation initiation factor 2-alpha (code XP_048641134.1), almost 38% identical with Spike:

Query  452  LYRLFRKSNLKPF-ERDISTE  471 Spike ACE2 binding domain
            ++  F     KPF E DI  +
Sbjct  277  IFAEFTSEKEKPFGECDIENQ  297 TIF2A
Query  485  GFNCYFPLQ-SYGFQP  489 SPIKE
            G  C      S    P
Sbjct  397  GHYCHRISTLSGQVCP  401      XP_048641134.1 = TIF2A

The ‘CHRIST’ section is gone again, except fot the first Cys residue.

Next protein reverse transcriptase/maturase family WP_087017951.1 with 71% identities(!!!) over 50% sequence coverage:

Query  446  GGNYNYLYRLFRKSNLKP  463 Spike 
            GG    +  L RKS   P
Sbjct  252  GGICHRISTLHRKSKNNP  269 WP_087017951.1 reverse transcriptase
Query 668 AGICASYQT-QTNSPRRARSVASQSIIAYTMSLGAEN---SVAYSNNS 711 FURINsite
           GIC    T    S     S   +  IA  + L  +     V   NN 
Sbjct 252 GGICHRISTLHRKSKNNPDSPDREKWIAEEVELKRQRVKIPVYQDNNK  299
Query  1246  GCCSCGSCCKFDEDDSEPVL  1265 Spike 
             G C    C      DSEPV+
Sbjct  541   GICELCGC------DSEPVV  554 WP_087017951.1
Query  1098  NGTHWFV  1104 Spike
             NGT+WF+
Sbjct  150   NGTKWFI  156 WP_087017951.1

In the above example 2 different Spike sections match the ‘CHRIST’ section from the reverse transcriptase. The high homology between Spike and reverse transcriptase is troubling, and like above, it does not contain the ‘CHRIST’ sections, except for one or two residues conservation.

The next protein chromatin modification-related protein EAF7-like XP_048006383.1 with less homology but still many highly homologous sections, just one as example:

Query  40   DKVFRSS--------VLHSTQDLFLPFFSNVTWFHAIHVSGTNGT  76
            D VFR+S        + H+T++     F  V   +    SG N +
Sbjct  406  DLVFRTSDSFENLEPIAHTTENFDNEEFEPVEEMREAQGSGANES  450

And when you see Nature articles title like this one:”SARS-CoV-2 restructures host chromatin architecture”, you might ask WTH (what the hell) is going on here? Have to put this new link to an interview with an incredibly suffering nurse:

VIDEO - Florida ER Nurse (Dawn) diagnosed with Alveolar Rhabdomyosarcoma (Turbo Cancer), 5 months after COVID-19 booster. She had 3 Moderna vaccines in total.

Dawn is mentioning a Forkhead protein related possibly to her cancers. The chromatin remodeling proteins do interact with forkheads in order to rearrange DNA strands. That’s why Forkheads do contains DNA binding domains (FOX-DBD) with known motifs, summary of which is accessible at https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501956/ . Table 1 of that pub lists the determined structures of these motifs, among others, one of those ‘GTAAACA’. Is it in the Spike? Sure it is (sorry for the increasing irony), right at the position 25091-25097 of the entire SARS-CoV-2 genome with 21563-25384 range covering the Spike (https://www.ncbi.nlm.nih.gov/nuccore/NC_045512). Pdb Data Bank entry at https://www.rcsb.org/fasta/entry/7CBY/display shows how that piece of HUMAN DNA (now in synthetic Spike genome) binds the human Forkhead box protein G1.

A large family of serine incorporator 4 proteins with example XP_045305889.1 contains the very unique cysteine rich section, very homologous to the Spike and very rare among proteins:

Query  1235  CCMTSCCSCLKGCC  1248 Spike
             CC  + C+C   CC
Sbjct  41    CCGPAPCTC---CC  51 serine incorporator 4
or by hand:
 CM-TSCCSCLKGCCSCGSCCK Spike
  +  SCC      C+C  CC+
 FYQVSCCGPAP--CTC--CCH Serine incorporator 4
 
Query  356  KRISN  360 Spike
             RIS 
Sbjct  510  HRIST  514 Serine incorporator 4
extention of the above by hand adding the C-terminal section
Query  356  YAWNRKRISNCV  360 Spike
            +    +RIS     <<< the highest homology with 'CHRIST' section
Sbjct  510  FRRQCHRISTAR  514 serine incorporator 4

The ‘CHRIST’ section in all Serine Incorporator Protein Families is located at the very C-terminal end and in case of this protein from Leopardus geoffroyi (Geoffroy's cat) (https://www.ncbi.nlm.nih.gov/protein/XP_045305889.1), it actually ends with almost the biblical inter-twinned words ‘CHRISTAR‘=CHRIST-STAR. Also in this case the serine incorporator 4 protein containing the sequence ‘CHRIST’ is connected with SARS-CoV-2^3.

Next WD-40 repeat protein located at https://www.ncbi.nlm.nih.gov/protein/PNY03708.1 . Here its few BLAST alignments with Spike:

Query 1109  FYEPQIITTDNTFVSGNCDVVIGIVNNTVYDPLQPE-----LDSFKEELD-KYFKNHTSP
            FY+P+++T +N+   G     +G   +TV  P+  E     +   ++ L+ +Y  +H   
Sbjct 733   FYQPEVLTNENSIDFGTTQ--LGGKLDTVKLPVWAENPIDFIHKHRKALESEYVSSHLHE 
here the ACE2 receptor bindinding domain:
Query  438  SNNLDSKVGGNYN--YLYR-LFRKSNLKPFERDISTEIYQAGST  478 Spike
            SN   +   G Y   +LYR L R+S L+ F  D S   +  GS+ <<IDENTITIES
Sbjct  483  SNETSATTDGVYKCEFLYRYLLRRSALELFMVDRSNFFFDFGSS  526 WD-40
Query  79   FDNPVLP-FNDGVYFAS  94 Spike 
            FD+PV+P F+ G +++S  << IDENTITIES
Sbjct  643  FDDPVIPKFHYGSHYSS  659 WD-40
and one of the highest scored aligned 'CHRIST' section:

Query  615  VNCTEVPVAIHADQLTPTWR  634 Spike 
            V C  +   IHA      WR
Sbjct  278  VTCHRISTGIHA------WR  291 WD-40 'CHRIST' section

and now the only best conserved 'CHRIST' section in Spike:
Query  354  NRKRISNCVADYSVLYNSASFSTFKC  379 Spike 
              +RI+  V +YS   ++ +   +KC
Sbjct  471  TSRRINFIVDNYSNETSATTDGVYKC  496 WD-40

Is there anything in common between WD-40 repeat like proteins with the WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly, and Spike??? Sure there is, the recent research, just published in the most prestigious journal, available at https://www.nature.com/articles/s41467-023-44076-3 ^4. This it the first time when the scientists talk about ‘genetic vaccines’, for a change… Here one sentence from their abstract, quote: “Because this C-terminal residue is the key determinant of SARS-CoV-2 assembly and fusogenicity our work provides a framework for the export of S protein encoded in genetic vaccines for surface display and immune activation“.

One more, this huge one, >5000 resides, its name MIDASIN (could be mid-a-SIN) with ~90% sequence coverage and ~40% IDENTITIES(!!) with Spike. It is s.c. AAA ATPase with vWA domain (i.e. Von Willebrand factor type A domain), involved in ribosome maturation (Translation, ribosomal structure and biogenesis):

Query  737   DCTMYICGDSTECSNLLLQYGSFCTQLNRALTG  769 Spike 
             D + Y CGDST  S+L+     F + L R + G
Sbjct  4956  DSSDYKCGDSTHSSSLM-----FYSNLKRIVMG  4983 Midasin
Query  132   EFQFCNDPFLGVYYHKNNKSWMESEFRVYSSANNCTFEYVSQPFLMDLEGKQGNFKN
             E   C   F  +   + N++W     RV S      F       +MD + K+GN+K 
Sbjct  1208  ERDLCVASFFVLVERQRNEAW---RARVKSIIEKWCF-------MMDRDDKKGNWKE
Query  1244  LKGCCSCG--SCCKFD-EDDSEP  1263 Spike 
             LK  C+ G     K D EDD E 
Sbjct  5140  LKRVCTVGVDRVLKLDSEDDQEN  5162 Mid-a-SIN

two Spike sections align with the 'CHRIST' motif in Mid-A-SIN

Query  1001 LQSLQTYVTQQLIRAAEIRA  1020 Spike
               + TYV+Q  I  + +RA
Sbjct  178  CHRISTYVSQHDIILSPVRA  197 Mid-A-SIN 'CHRIST-1'section
Query  354  NRKRISNCVADYSVLYNSASFSTFKCYGVSPTKLNDLCFTNVY  396 Spike
              +RIS  V+ + ++ +       K +     K++     N+Y
Sbjct  180  FCHRISTYVSQHDIILSPVRADDVKVFCDGIEKISTEIRKNLY  219 Mid-A-SIN
=> the 'KRIS'section of Spike shows the highest homology found by BLAST

And is that Mid-A-SIN with its Von Willebrand factor type A domain somewhat related to covid19?? Of course it is, a big time, here only two citations ^5,^6, out of countless more…

This one is also special, CRISPR/Cas system-associated protein Cas3, taken out of human oral metagenome with sequence in https://www.ncbi.nlm.nih.gov/protein/PIE47861.1. Here just few alignments, including the ‘CHRIST’ section in comparison with Spike:

Query  451  YLYRLFRKSNLKPFERDISTEIYQAGSTPCNGVEGFNCYFPLQS  494 Spike RBD
            ++Y  F  +N KP   DIS  I +      +     N  F + S
Sbjct  948  FIYPGFETNNFKPHSYDISELITENQLARIDAQARINNNFAMDS  991 Cas3
Query  134  QFCNDPFLGV-----YYHKNNKS  151 Spike
            Q CND   GV      YHK +KS
Sbjct  762  QLCNDLMQGVIQLHQRYHKLDKS  784 Cas3

and now THREE(!!!) Spike pieces aligned with 'CHRIST' section in Cas3:

Query  365  YSVLYNSASFST-FKCYGVSPTKL-------------NDLCFTNV  395 Spike
            Y +L +SAS ST   C  +S  KL             N+L +  V
Sbjct  46   YQLLKDSASRSTAVSCHRISTRKLTKLVWIVGNKRKFNELGYVAV  90 Cas3
Query  669  GICASYQTQTNSPRRARSVASQSIIAY  695       Spike FURIN site!!!
            G+ + YQ   +S  R+ +V+   I +
Sbjct  41   GLRTVYQLLKDSASRSTAVSCHRISTR  67        Cas3
Query  347  FASVYAWNRKRISNCVADYSVLYNSASFST-FKCYGVSPTKLNDLCF  392
              +V              Y +L +SAS ST   C+ +S  KL  L +
Sbjct  42   LRTV--------------YQLLKDSASRSTAVSCHRISTRKLTKLVW  74

For this one that’s not even a question to relate it to SARS-CoV-2, this time, to its detection^7,^8…

And few more examples:

DNA endonuclease rbbp8      KAI8505736.1 
Query  1069  PAQEKNFTTAPAICHDGKA 1086 Spike
             PA +      PA CH   +
Sbjct  43    PAADGAEPDTPAPCHRIST  60 rbb8

Toll/interleukin-1 receptor domain-containing protein [Oscillospiraceae bacterium] MBR4036625.1
Query  229  LPIGINITRFQTLLALHRSYL  246 Spike 
            L +GI    F   +  HR
Sbjct  538  LVMGIVENPFNWYVDCHRIST  555 Toll receptor

Pseudomonas phosphoenolpyruvate--protein phosphotransferase (PtsA)
Query  10   LVSSQCVNLTTRT-QLPPAYTNSFTRGVYYP  39
            L ++QC  ++T    LP A         ++P
Sbjct  805  LDAAQCHRISTDLLNLPSAAAVRQACHQHWP  835

A special addition, because of its importance in governmental interests (DOE, LBNL, Los Alamos National Laboratory), it is a fungal protein from HET-R family. A review from 2000^9 describes that cell fusions in fungi can lead to cells with different nuclear types forming s.c. heterokaryons, genetically controlled by specific loci termed het loci (for heterokaryon incompatibility). From that 2000 abstract: “Heterokaryotic cells formed between individuals of unlike het genotypes undergo a characteristic cell death reaction or else are severely inhibited in their growth.” Here some of the alignment of HET-R protein with Spike (this time in Sbjct line):

Query  79   PVRVVVYS  86  HET-R  
            P RVVV S
Sbjct  507  PYRVVVLS  514 SARS-CoV-2 Spike
Query  640   DVSGLNS  646 HET-R  
             D+SG+N+
Sbjct  1168  DISGINA  1174  SARS-CoV-2 Spike
Query  259  QIFSGSSDGTLRVWDVQSGTCRHTISGHGDNVNCVA  294  HET-R  
            ++F+ +   ++  W+      R  IS      NCVA
Sbjct  340  EVFNATRFASVYAWN------RKRIS------NCVA  363 SARS-CoV-2 Spike
Query  167  VYSPKGDQVASGCADSSVRLWNVASG  HET-R    
            VY+    ++++  AD SV L+N AS  
Sbjct  349  VYAWNRKRISNCVADYSV-LYNSASF  SARS-CoV-2 Spike
Query  391   YDGTMRLWDVDTGTCHRISTGHTS  414  HET-R  
             YD      D       +    HTS
Sbjct  1138  YDPLQPELDSFKEELDKYFKNHTS  1161 SARS-CoV-2 Spike
and last with manual adition:
              SPRRARSVASQ  >>SARS-CoV-2 Spike Furin Site
              SP+   VAS
Query  168  VYSPKGDQVASGCADSSVRLWNVASGECSHIF    HET-R  
            VY+    ++++  AD SV L+N AS      +
Sbjct  350  VYAWNRKRISNCVADYSV-LYNSASFSTFKCY    SARS-CoV-2 Spike
  

There are so many, many more proteins with the above features. But that above implies to me already, that Spike was build from relevant proteins which contain the amino acids sequence, that short peptide ‘CHRIST’, which during the incorporation was overwritten with different amino acids (code) in highly homologous sections. All those proteins carrying the word related to CHRISTmas are also closely related with specific SARS-CoV-2 characteristics. It is as if one can take all the proteins containing the special sequence ‘CHRIST’ (without even concentrating on species), and their functions will be related to Spike, while not having that sequence anymore in Spike.

On the other hand that highest homology tripeptide ‘RIS’ from the last BLAST output above, in the Spike and the ‘Serine Incorporator 4’has its short homolog in protein called luciferase (NIH data location at https://www.ncbi.nlm.nih.gov/protein/UUA44467.1 ). BLAST finds one hit with the Spike ‘RIS’ section, the second was found by human eyes:

Query  386  QRGELCV  392 Luciferase
         GVNQRGELCVRGPM
            +R   CV
         WNRKRISNCVADYS
Sbjct  356  KRISNCV  362 Spike
now by hand, a different part of Luciferase overlaps better with Spike:
GLNTNHRIVVCS Luciferase 
     ++I  C
YAWNRKRISNCV Spike2020
or when adding gaps:
GLNTNH-RIVVCS Luciferase 
    N+ RI  C
YAW-NRKRISNCV Spike2020

We know SARS-CoV-2, its Spike in particular, was designed over a period of many years, ending with countless patents. Current bioinformatics search for anything related to Spike, ends up with many, many thousands of Spike closely related ‘variants’, to a level where in fact one can’t find anything, but the Spike. A digital bio-invasion, in my opinion. If the ‘Spike origin idea’ presented here, has nevertheless some meaning in reality, if it is indeed true (it looks to me like it is), then imagine the amount of HATE that ‘somebody’ (who pays for all this ‘modern science’) must have against the ORIGINAL CREATOR, GOD. That hate must be immense, based on incredible jealousy, resulting in overwriting the original genetic code, with the one, which does not carry the word ‘CHRIST’ any more.

Dr. Fauci (Jesuit) and his connection with this special day was mentioned exactly a year ago, in a post at, with quite few non-existing links any more:

Thank you for your attention.

Literature:

1. David G Alleva et al. “Development of an IgG-Fc fusion COVID-19 subunit vaccine, AKS-452“ Vaccine 2021 Oct 29;39(45):6601-6613. https://pubmed.ncbi.nlm.nih.gov/34642088/

2. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955571/

3. Shaofen Xu et al. “The Emerging Role of the Serine Incorporator Protein Family in Regulating Viral Infection“ Front Cell Dev Biol. 2022; 10: 856468. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9010877/

4. Debajit Dey et al. “A single C-terminal residue controls SARS-CoV-2 spike trafficking and incorporation into VLPs” Nature Communications | (2023)14:8358 https://www.nature.com/articles/s41467-023-44076-3

5. Yoshihiro Fujimura ^{#  1} , Linda Z Holland “COVID-19 microthrombosis: unusually large VWF multimers are a platform for activation of the alternative complement pathway under cytokine storm“ Int J Hematol. 2022 Apr;115(4):457-469.https://pubmed.ncbi.nlm.nih.gov/35316498/

6. Kan Li et al. “SARS-CoV-2 Spike protein promotes vWF secretion and thrombosis via endothelial cytoskeleton-associated protein 4 (CKAP4)“ Signal Transduction and Targeted Therapy volume 7, Article number: 332 (2022). https://www.nature.com/articles/s41392-022-01183-9

7. Pallavi Deol et al. “CRISPR use in diagnosis and therapy for COVID-19“ Methods in Microbiology. 2022; 50: 123–150. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073596/

8. Kazuto Yoshimi e tal. “CRISPR-Cas3-based diagnostics for SARS-CoV-2 and influenza virus“ iScience. 2022 Feb 18; 25(2): 103830. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8801231/

9. Sven J. Saupe “Molecular Genetics of Heterokaryon Incompatibility in Filamentous Ascomycetes” Microbiol Mol Biol Rev. 2000 Sep; 64(3): 489–502. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC99001/