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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 2 |
2010 | 2 |
2016 | 1 |
2017 | 1 |
2019 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 54872
7 results
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Page 1
PIGG variant pathogenicity assessment reveals characteristic features within 19 families.
Genet Med. 2021 Oct;23(10):1873-1881. doi: 10.1038/s41436-021-01215-9. Epub 2021 Jun 10.
Genet Med. 2021.
PMID: 34113002
Free PMC article.
Identification and In Silico Characterization of a Novel Point Mutation within the Phosphatidylinositol Glycan Anchor Biosynthesis Class G Gene in an Iranian Family with Intellectual Disability.
Parsamanesh N, Safarpour H, Etesam S, Shadmehri AA, Miri-Moghaddam E.
Parsamanesh N, et al.
J Mol Neurosci. 2019 Dec;69(4):538-545. doi: 10.1007/s12031-019-01376-y. Epub 2019 Aug 14.
J Mol Neurosci. 2019.
PMID: 31414351
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Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of function.
Zhao JJ, Halvardson J, Knaus A, Georgii-Hemming P, Baeck P, Krawitz PM, Thuresson AC, Feuk L.
Zhao JJ, et al.
Hum Mutat. 2017 Oct;38(10):1394-1401. doi: 10.1002/humu.23268. Epub 2017 Jun 12.
Hum Mutat. 2017.
PMID: 28581210
Free PMC article.
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Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia.
Makrythanasis P, Kato M, Zaki MS, Saitsu H, Nakamura K, Santoni FA, Miyatake S, Nakashima M, Issa MY, Guipponi M, Letourneau A, Logan CV, Roberts N, Parry DA, Johnson CA, Matsumoto N, Hamamy H, Sheridan E, Kinoshita T, Antonarakis SE, Murakami Y.
Makrythanasis P, et al.
Am J Hum Genet. 2016 Apr 7;98(4):615-26. doi: 10.1016/j.ajhg.2016.02.007. Epub 2016 Mar 17.
Am J Hum Genet. 2016.
PMID: 26996948
Free PMC article.
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Association of genetic variants with hemorrhagic stroke in Japanese individuals.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y.
Yoshida T, et al.
Int J Mol Med. 2010 Apr;25(4):649-56. doi: 10.3892/ijmm_00000388.
Int J Mol Med. 2010.
PMID: 20198315
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Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals.
Oguri M, Kato K, Yokoi K, Yoshida T, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y.
Oguri M, et al.
Am J Hypertens. 2010 Jan;23(1):70-7. doi: 10.1038/ajh.2009.190. Epub 2009 Oct 22.
Am J Hypertens. 2010.
PMID: 19851296
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Association of gene polymorphisms with chronic kidney disease in Japanese individuals.
Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nozawa Y, Yamada Y.
Yoshida T, et al.
Int J Mol Med. 2009 Oct;24(4):539-47. doi: 10.3892/ijmm_00000263.
Int J Mol Med. 2009.
PMID: 19724895
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