Paper · 468260
Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).
Dallapiccola B and 4 others. Hum Genet, 1979. Cited by 20 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12). Papers, record 468260. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/468260
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Increased HK1 activity levels in the red cells of a patient with a de novo trisomy 10p: t(Y;10)(p11;p12).
- PubMed
Topics13
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Chromosomes, Human, 6-12 and X | Major topic |
| Erythrocytes | Major topic |
| Hexokinase | Major topic |
| Sex Chromosomes | Major topic |
| Trisomy | Major topic |
| Y Chromosome | Major topic |
| Cell Survival | |
| Chromosome Mapping | |
| Congenital Abnormalities | |
| Humans | |
| Intellectual Disability | |
| Male | |
| Syndrome |
Source PubMed
Grants0
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
None in this release.
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References7
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 640,658 | Partial trisomy 10p in two generations. | Hum Genet | 1978 | https://conductscience.org/library/papers/640658 | PubMed |
| 2 | 17,494,625 | Localization of the structural genes for hexokinase-1 and inorganic pyrophosphatase on region (pter-->q24) of human chromosome 10. | Cytogenet Cell Genet | 1976 | https://conductscience.org/library/papers/17494625 | PubMed |
| 3 | 4,827,482 | Proceedings: Synteny of human genes for glutamic oxalacetic transaminase and hexokinase in somatic cell hybrids. | Cytogenet Cell Genet | 1974 | https://conductscience.org/library/papers/4827482 | PubMed |
| 4 | 669,709 | 10q(q23 leads to qter) duplication: GOTs, HK1, and other gene markers. | Hum Genet | 1978 | https://conductscience.org/library/papers/669709 | PubMed |
| 5 | 913,435 | New chromosomal dysmorphic syndromes. 2. Trisomy 10p. | Eur J Pediatr | 1977 | https://conductscience.org/library/papers/913435 | PubMed |
| 6 | 929,180 | Mapping the locus of the H-Y gene on the human Y chromosome. | Science | 1977 | https://conductscience.org/library/papers/929180 | PubMed |
| 7 | 703,400 | Relationship between glucose phosphorylating activities and erythrocyte age. | Mech Ageing Dev | 1978 | https://conductscience.org/library/papers/703400 | PubMed |
Cited by9
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 20 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 34,513,343 | Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature. | Cureus | 2021 | https://conductscience.org/library/papers/34513343 | PubMed |
| 28,458,900 | Congenital hyperinsulinism and Poland syndrome in association with 10p13-14 duplication. | Endocrinol Diabetes Metab Case Rep | 2017 | https://conductscience.org/library/papers/28458900 | PubMed |
| 21,438,145 | Familial 6p22.2 duplication associates with mild developmental delay and increased SSADH activity. | Am J Med Genet B Neuropsychiatr Genet | 2011 | https://conductscience.org/library/papers/21438145 | PubMed |
| 7,160,850 | Regional mapping of the locus for hexokinase-1 (HK1) | Hum Genet | 1982 | https://conductscience.org/library/papers/7160850 | PubMed |
| 7,106,753 | Regional mapping of the locus for hexokinase-1 (HK1) to 10p11 equals to q23 by gene dosage in human fibroblasts. | Hum Genet | 1982 | https://conductscience.org/library/papers/7106753 | PubMed |
| 7,017,147 | Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome. | J Med Genet | 1981 | https://conductscience.org/library/papers/7017147 | PubMed |
| 6,842,544 | Partial monosomy of chromosome 10 short arms. | J Med Genet | 1983 | https://conductscience.org/library/papers/6842544 | PubMed |
| 6,236,690 | Duplication of chromosome 10p: confirmation of regional assignments of platelet-type phosphofructokinase. | Am J Hum Genet | 1984 | https://conductscience.org/library/papers/6236690 | PubMed |
| 6,146,563 | A de novo case of trisomy 10p: gene dosage studies of hexokinase, inorganic pyrophosphatase and adenosine kinase. | Hum Genet | 1984 | https://conductscience.org/library/papers/6146563 | PubMed |
Genes4
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| G6PD | 2,539 | PubTator's text mining | https://conductscience.org/library/genes/2539 | NCBI Gene |
| GPI | 2,821 | PubTator's text mining | https://conductscience.org/library/genes/2821 | NCBI Gene |
| HK1 | 3,098 | PubTator's text mining | https://conductscience.org/library/genes/3098 | NCBI Gene |
| PGD | 5,226 | PubTator's text mining | https://conductscience.org/library/genes/5226 | NCBI Gene |
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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