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2011 1
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31 results

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Pedigree-based study to identify GOLGB1 as a risk gene for bipolar disorder.
Liu FR, Zhou Y, Wang Y, Huang LL, Zhang X, Luo H, Wu SY, Lyu HY, Huang LH, Xu H, Zhang YW. Liu FR, et al. Transl Psychiatry. 2022 Sep 17;12(1):390. doi: 10.1038/s41398-022-02163-x. Transl Psychiatry. 2022. PMID: 36115840 Free PMC article.
In the present study, we carried out whole genome sequencing for a Chinese BD family with three affected members and three unaffected members, and identified multiple candidate causal variations, including a frameshift mutation in the GOLGB1 gene. Since a GOLGB1 mis …
In the present study, we carried out whole genome sequencing for a Chinese BD family with three affected members and three unaffected member …
Golgb1 regulates protein glycosylation and is crucial for mammalian palate development.
Lan Y, Zhang N, Liu H, Xu J, Jiang R. Lan Y, et al. Development. 2016 Jul 1;143(13):2344-55. doi: 10.1242/dev.134577. Epub 2016 May 25. Development. 2016. PMID: 27226319 Free PMC article.
Through genetic linkage mapping and whole-exome sequencing, we identified a loss-of-function mutation in the Golgb1 gene that co-segregated with cleft palate in a new mutant mouse line. Golgb1 is a ubiquitously expressed large coiled-coil protein, also known as gian …
Through genetic linkage mapping and whole-exome sequencing, we identified a loss-of-function mutation in the Golgb1 gene that co-segr …
CIBERSORT analysis of TCGA and METABRIC identifies subgroups with better outcomes in triple negative breast cancer.
Craven KE, Gökmen-Polar Y, Badve SS. Craven KE, et al. Sci Rep. 2021 Feb 25;11(1):4691. doi: 10.1038/s41598-021-83913-7. Sci Rep. 2021. PMID: 33633150 Free PMC article.
Twenty-five genes showed mutational frequency differences between the TCGA high and low T cell groups, and many play important roles in inflammation or immune evasion (ATG2B, HIST1H2BC, PKD1, PIKFYVE, TLR3, NOTCH3, GOLGB1, CREBBP). Identification of these mutations suggest …
Twenty-five genes showed mutational frequency differences between the TCGA high and low T cell groups, and many play important roles in infl …
A novel low-grade nasopharyngeal adenocarcinoma characterized by a GOLGB1-BRAF fusion gene.
Bubola J, Antonescu CR, Weinreb I, Swanson D, De Almeida JR, MacMillan CM, Dickson BC. Bubola J, et al. Genes Chromosomes Cancer. 2021 Jan;60(1):49-53. doi: 10.1002/gcc.22897. Epub 2020 Sep 29. Genes Chromosomes Cancer. 2021. PMID: 32951290 Free PMC article.
Subsequent RNA sequencing was performed which identified a novel GOLGB1-BRAF fusion product. Based on its unique morphology and molecular findings, this is presumed to represent a novel subtype of nasopharyngeal adenocarcinoma. ...
Subsequent RNA sequencing was performed which identified a novel GOLGB1-BRAF fusion product. Based on its unique morphology and molec …
Association between GOLGB1 tag-polymorphisms and nonsyndromic cleft palate only in the Brazilian population.
Machado RA, Martelli-Júnior H, de Almeida Reis SR, Persuhn DC, Coletta RD. Machado RA, et al. Ann Hum Genet. 2018 Jul;82(4):227-231. doi: 10.1111/ahg.12242. Epub 2018 Feb 12. Ann Hum Genet. 2018. PMID: 29430628
Genetic variants in golgin subfamily B member 1 (GOLGB1), a gene that is essential for normal murine palatogenesis, were analyzed in this study to establish its potential association with NSCPO risk in the Brazilian population. ...Our results suggest that common polymorphi …
Genetic variants in golgin subfamily B member 1 (GOLGB1), a gene that is essential for normal murine palatogenesis, were analyzed in …
A Novel 65-bp Indel in the GOLGB1 Gene Is Associated with Chicken Growth and Carcass Traits.
Fu R, Ren T, Li W, Liang J, Mo G, Luo W, He D, Liang S, Zhang X. Fu R, et al. Animals (Basel). 2020 Mar 12;10(3):475. doi: 10.3390/ani10030475. Animals (Basel). 2020. PMID: 32178328 Free PMC article.
Golgin subfamily B member 1 (GOLGB1) gene encodes the coat protein 1 vesicle inhibiting factor, giantin. Previous study showed that mutations of the GOLGB1 gene are associated with dozens of human developmental disorders and diseases. However, the biological functio …
Golgin subfamily B member 1 (GOLGB1) gene encodes the coat protein 1 vesicle inhibiting factor, giantin. Previous study showed that m …
Insertional mutation in the Golgb1 gene is associated with osteochondrodysplasia and systemic edema in the OCD rat.
Katayama K, Sasaki T, Goto S, Ogasawara K, Maru H, Suzuki K, Suzuki H. Katayama K, et al. Bone. 2011 Nov;49(5):1027-36. doi: 10.1016/j.bone.2011.08.001. Epub 2011 Aug 7. Bone. 2011. PMID: 21851869
Fine linkage mapping localized the ocd locus within 84kb of positions 65,584-65,668kb containing a part of Golgb1 gene on chromosome 11. Expression of Golgb1 mRNA was found in limb buds, somite derivatives and calvaria. Sequence analysis identified a 10-bp insertion …
Fine linkage mapping localized the ocd locus within 84kb of positions 65,584-65,668kb containing a part of Golgb1 gene on chromosome …
Fusion of PDGFRB to MPRIP, CPSF6, and GOLGB1 in three patients with eosinophilia-associated myeloproliferative neoplasms.
Naumann N, Schwaab J, Metzgeroth G, Jawhar M, Haferlach C, Göhring G, Schlegelberger B, Dietz CT, Schnittger S, Lotfi S, Gärtner M, Dang TA, Hofmann WK, Cross NC, Reiter A, Fabarius A. Naumann N, et al. Genes Chromosomes Cancer. 2015 Dec;54(12):762-70. doi: 10.1002/gcc.22287. Epub 2015 Sep 10. Genes Chromosomes Cancer. 2015. PMID: 26355392
We here report the identification of three new PDGFRB fusion genes in three male MPN-eo patients: MPRIP-PDGFRB in a case with t(5;17)(q33;p11), CPSF6-PDGFRB in a case with t(5;12)(q33;q15), and GOLGB1-PDGFRB in a case with t(3;5)(q13;q33). The fusion proteins identified by …
We here report the identification of three new PDGFRB fusion genes in three male MPN-eo patients: MPRIP-PDGFRB in a case with t(5;17)(q33;p1 …
Polymorphisms in three genes are associated with hemorrhagic stroke.
Liu W, Ge S, Liu Y, Wei C, Ding Y, Chen A, Wu Q, Zhang Y. Liu W, et al. Brain Behav. 2015 Oct 1;5(11):e00395. doi: 10.1002/brb3.395. eCollection 2015 Nov. Brain Behav. 2015. PMID: 26664786 Free PMC article.
BACKGROUND: Multiligand receptor for advanced glycation end products (RAGE), osteoprotegerin, and Golgb1 genes may be implicated in atherosclerosis and vascular diseases. Single nucleotide polymorphisms (SNPs) rs1035798 in RAGE gene, rs2073617 and rs2073618 in TNFRSF11B, a …
BACKGROUND: Multiligand receptor for advanced glycation end products (RAGE), osteoprotegerin, and Golgb1 genes may be implicated in a …
Golga5 is dispensable for mouse embryonic development and postnatal survival.
McGee LJ, Jiang AL, Lan Y. McGee LJ, et al. Genesis. 2017 Jul;55(7):10.1002/dvg.23039. doi: 10.1002/dvg.23039. Epub 2017 Jun 2. Genesis. 2017. PMID: 28509431 Free PMC article.
Moreover, whereas Golga5 is structurally closely related to Golgb1, we show that inactivation of Golga5 does not enhance the severity of developmental defects in Golgb1-deficient mice. ...
Moreover, whereas Golga5 is structurally closely related to Golgb1, we show that inactivation of Golga5 does not enhance the severity …
31 results