Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2013 2
2014 2
2015 3
2016 2
2017 2
2018 2
2019 3
2021 2
2022 4
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

21 results

Results by year

Filters applied: . Clear all
Page 1
Enzyme assay of β1,3-glycosyltransferase family.
Togayachi A. Togayachi A. 2021 Dec 20 [updated 2022 Mar 28]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. 2021 Dec 20 [updated 2022 Mar 28]. In: Nishihara S, Angata K, Aoki-Kinoshita KF, Hirabayashi J, editors. Glycoscience Protocols (GlycoPODv2) [Internet]. Saitama (JP): Japan Consortium for Glycobiology and Glycotechnology; 2021–. PMID: 37590747 Free Books & Documents. Review. No abstract available.
TINAGL1 and B3GALNT1 are potential therapy target genes to suppress metastasis in non-small cell lung cancer.
Umeyama H, Iwadate M, Taguchi YH. Umeyama H, et al. BMC Genomics. 2014;15 Suppl 9(Suppl 9):S2. doi: 10.1186/1471-2164-15-S9-S2. Epub 2014 Dec 8. BMC Genomics. 2014. PMID: 25521548 Free PMC article.
These genes are potential target genes for the therapy of NSCLC. Among the eleven genes, TINAGL1 and B3GALNT1 are possible candidates for drug compounds that inhibit their gene expression....
These genes are potential target genes for the therapy of NSCLC. Among the eleven genes, TINAGL1 and B3GALNT1 are possible candidates …
Multiple miscarriages in two sisters of Thai origin with the rare P(k) phenotype caused by a novel nonsense mutation at the B3GALNT1 locus.
Ricci Hagman J, Hult AK, Westman JS, Hosseini-Maaf B, Jongruamklang P, Saipin J, Bejrachandra S, Olsson ML. Ricci Hagman J, et al. Transfus Med. 2019 Jun;29(3):202-208. doi: 10.1111/tme.12544. Epub 2018 Jun 6. Transfus Med. 2019. PMID: 29873420
Inactivating mutations in the 3-beta-N-acetylgalactosaminyltransferase gene (B3GALNT1) give rise to the rare P(k) phenotype, which lack the P and PX2 antigens. ...CONCLUSION: We describe a novel nonsense mutation (c.420T>G) in B3GALNT1 (GLOB*01N.13), which was ad …
Inactivating mutations in the 3-beta-N-acetylgalactosaminyltransferase gene (B3GALNT1) give rise to the rare P(k) phenotype, which la …
Promoter identification and analysis of key glycosphingolipid biosynthesis-globo series pathway genes in piglets.
Qin WY, Gan LN, Xia RW, Dong WH, Sun SY, Zhu GQ, Wu SL, Bao WB. Qin WY, et al. Genet Mol Res. 2017 Jun 29;16(2). doi: 10.4238/gmr16029574. Genet Mol Res. 2017. PMID: 28671252 Free article.
Glycosphingolipid biosynthesis-globo series pathway genes (FUT1, FUT2, ST3GAL1, HEXA, HEXB, B3GALNT1, and NAGA) play an important regulatory role in the defense against Escherichia coli F18 in piglets. ...The promoters of glycosphingolipid biosynthesis genes identified con …
Glycosphingolipid biosynthesis-globo series pathway genes (FUT1, FUT2, ST3GAL1, HEXA, HEXB, B3GALNT1, and NAGA) play an important reg …
An update on the GLOB blood group system and collection.
Hellberg A, Westman JS, Olsson ML. Hellberg A, et al. Immunohematology. 2013;29(1):19-24. Immunohematology. 2013. PMID: 24046919 Review.
The molecular genetic basis of globoside deficiency is absence of functional P synthase as a result of mutations at the B3GALNT1 locus. Other related glycolipid structures, the LKE and PX2 antigens, remain in the GLOB blood group collection pending further evidence about t …
The molecular genetic basis of globoside deficiency is absence of functional P synthase as a result of mutations at the B3GALNT1 locu …
Globoside Is Dispensable for Parvovirus B19 Entry but Essential at a Postentry Step for Productive Infection.
Bieri J, Ros C. Bieri J, et al. J Virol. 2019 Sep 30;93(20):e00972-19. doi: 10.1128/JVI.00972-19. Print 2019 Oct 15. J Virol. 2019. PMID: 31341051 Free PMC article.
With the aim of clarifying the role of Gb4 as a B19V receptor, we knocked out the gene B3GalNT1 coding for the enzyme globoside synthase in UT7/Epo cells. Consequently, B3GalNT1 transcripts and Gb4 became undetectable in the knockout (KO) cells without affecting cel …
With the aim of clarifying the role of Gb4 as a B19V receptor, we knocked out the gene B3GalNT1 coding for the enzyme globoside synth …
Identification of the Molecular and Genetic Basis of PX2, a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes.
Westman JS, Benktander J, Storry JR, Peyrard T, Hult AK, Hellberg Å, Teneberg S, Olsson ML. Westman JS, et al. J Biol Chem. 2015 Jul 24;290(30):18505-18. doi: 10.1074/jbc.M115.655308. Epub 2015 Jun 8. J Biol Chem. 2015. PMID: 26055721 Free PMC article.
We encountered a patient with mutations in B3GALNT1 causing the rare P-deficient P1 (k) phenotype and whose pretransfusion plasma was unexpectedly incompatible with p erythrocytes. ...Thin-layer chromatography, mass spectrometry, and flow cytometry were used to show that t …
We encountered a patient with mutations in B3GALNT1 causing the rare P-deficient P1 (k) phenotype and whose pretransfusion plasma was …
Expression of key glycosphingolipid biosynthesis-globo series pathway genes in Escherichia coli F18-resistant and Escherichia coli F18-sensitive piglets.
Dong WH, Dai CH, Sun L, Wang J, Sun SY, Zhu GQ, Wu SL, Bao WB. Dong WH, et al. Anim Genet. 2016 Aug;47(4):428-35. doi: 10.1111/age.12428. Epub 2016 Mar 11. Anim Genet. 2016. PMID: 26970430

The expression level of FUT1 was extremely significantly positively correlated with FUT2 and B3GALNT1 expression (P < 0.01) and also had a significant positive correlation with NAGA expression (P < 0.05). ...FUT1, ST3GAL1, B3GALNT1 and NAGA may also participat

…

The expression level of FUT1 was extremely significantly positively correlated with FUT2 and B3GALNT1 expression (P < 0.01) and al

…
An update on the GLOB blood group system (and former GLOB collection).
Ricci Hagman J, Westman JS, Hellberg Å, Olsson ML. Ricci Hagman J, et al. Immunohematology. 2018 Dec;34(4):161-163. Immunohematology. 2018. PMID: 30624951
The high-prevalence PX2 antigen, originally recognized as the x2 glycosphingolipid, is expressed on red blood cells of most individuals and is elevated in the rare PP1Pk-negative p blood group phenotype. P synthase, encoded by B3GALNT1, was found to elongate paragloboside …
The high-prevalence PX2 antigen, originally recognized as the x2 glycosphingolipid, is expressed on red blood cells of most individuals and …
21 results