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

Year Number of Results
1991 1
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2010 1
2011 2
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2017 1
2022 2
2024 0

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11 results

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Page 1
Venous Invasion in Colorectal Cancer: Impact of Morphologic Findings on Detection Rate.
Hwang C, Lee S, Kim A, Kim YG, Ahn SJ, Park DY. Hwang C, et al. Cancer Res Treat. 2016 Oct;48(4):1222-1228. doi: 10.4143/crt.2015.429. Epub 2016 Feb 12. Cancer Res Treat. 2016. PMID: 26875194 Free PMC article.
PURPOSE: Venous invasion (VI) is widely accepted as a poor prognostic factor in colorectal cancer (CRC), and is indicated as a high-risk factor determining the use of adjuvant chemotherapy in CRC. ...
PURPOSE: Venous invasion (VI) is widely accepted as a poor prognostic factor in colorectal cancer (CRC), and is indicated as a high-r …
Niemann-Pick type A disease with new mutation: a case report.
Aghamahdi F, Nirouei M, Savad S. Aghamahdi F, et al. J Med Case Rep. 2022 Jul 27;16(1):288. doi: 10.1186/s13256-022-03486-5. J Med Case Rep. 2022. PMID: 35883096 Free PMC article.
Type A is a rare, untreatable disease with early manifestations and a poor prognosis, with newborns rarely surviving for 2-3 years. CASE PRESENTATION: A 1-year-old Persian boy was referred to our clinic due to abdominal distention and poor weight gain. ...
Type A is a rare, untreatable disease with early manifestations and a poor prognosis, with newborns rarely surviving for 2-3 years. C …
Human newborns match tongue protrusion of disembodied human and robotic mouths.
Soussignan R, Courtial A, Canet P, Danon-Apter G, Nadel J. Soussignan R, et al. Dev Sci. 2011 Mar;14(2):385-94. doi: 10.1111/j.1467-7687.2010.00984.x. Dev Sci. 2011. PMID: 22213907
Results also showed progressively more accurate matching (full tongue protrusion) throughout repeated exposure to each kind of stimulus. Such findings are not in line with the predictions of the innate releasing mechanism (IRM) model or of the oral exploration hypothesis. …
Results also showed progressively more accurate matching (full tongue protrusion) throughout repeated exposure to each kind of stimulus. Suc …
A novel mutation in CLCN1 associated with feline myotonia congenita.
Gandolfi B, Daniel RJ, O'Brien DP, Guo LT, Youngs MD, Leach SB, Jones BR, Shelton GD, Lyons LA. Gandolfi B, et al. PLoS One. 2014 Oct 30;9(10):e109926. doi: 10.1371/journal.pone.0109926. eCollection 2014. PLoS One. 2014. PMID: 25356766 Free PMC article.
Direct sequencing of CLCN1 revealed a mutation disrupting a donor splice site downstream of exon 16 in only the affected cats. In vitro translation of the mutated protein predicted a premature truncation and partial lack of the highly conserved CBS1 (cystathionine beta-syn …
Direct sequencing of CLCN1 revealed a mutation disrupting a donor splice site downstream of exon 16 in only the affected cats. In vitro tran …
A FOXG1 mutation in a boy with congenital variant of Rett syndrome.
Le Guen T, Bahi-Buisson N, Nectoux J, Boddaert N, Fichou Y, Diebold B, Desguerre I, Raqbi F, Daire VC, Chelly J, Bienvenu T. Le Guen T, et al. Neurogenetics. 2011 Feb;12(1):1-8. doi: 10.1007/s10048-010-0255-4. Epub 2010 Aug 24. Neurogenetics. 2011. PMID: 20734096 Review.
Altogether the presentation in this male patient is highly reminiscent of that observed in FOXG1-mutated females with the congenital variant of Rett syndrome. This new case confirms the prediction that congenital variant of Rett syndrome should be found also in males, with …
Altogether the presentation in this male patient is highly reminiscent of that observed in FOXG1-mutated females with the congenital variant …
A homozygous frame-shift variant in PROSER1 is associated with developmental delay, hypotonia, genitourinary malformations, and distinctive facial features.
Salah A, Almannai M, Al Ojaimi M, Radefeldt M, Gulati N, Iqbal M, Alawbathani S, Al-Ali R, Beetz C, El-Hattab AW. Salah A, et al. Clin Genet. 2022 May;101(5-6):565-570. doi: 10.1111/cge.14126. Epub 2022 Mar 13. Clin Genet. 2022. PMID: 35229282
Therefore, PROSER1 may play vital and potentially general roles in gene regulation, consistent with the wide phenotypic spectrum observed in the individuals presented here. The consistent phenotype, the loss-of-function predicted from the frame-shift, the co-segregation of …
Therefore, PROSER1 may play vital and potentially general roles in gene regulation, consistent with the wide phenotypic spectrum observed in …
Venous invasion in colorectal cancer: impact of an elastin stain on detection and interobserver agreement among gastrointestinal and nongastrointestinal pathologists.
Kirsch R, Messenger DE, Riddell RH, Pollett A, Cook M, Al-Haddad S, Streutker CJ, Divaris DX, Pandit R, Newell KJ, Liu J, Price RG, Smith S, Parfitt JR, Driman DK. Kirsch R, et al. Am J Surg Pathol. 2013 Feb;37(2):200-10. doi: 10.1097/PAS.0b013e31826a92cd. Am J Surg Pathol. 2013. PMID: 23108018
Venous invasion (VI) is an independent prognostic indicator in colorectal cancer and may prompt consideration for adjuvant chemotherapy in patients with stage II tumors. ...
Venous invasion (VI) is an independent prognostic indicator in colorectal cancer and may prompt consideration for adjuvant chemothera …
Use of an elastic stain to show venous invasion in colorectal carcinoma: a simple technique for detection of an important prognostic factor.
Howlett CJ, Tweedie EJ, Driman DK. Howlett CJ, et al. J Clin Pathol. 2009 Nov;62(11):1021-5. doi: 10.1136/jcp.2009.065615. J Clin Pathol. 2009. PMID: 19861561
BACKGROUND: Venous invasion (VI) is an important prognostic factor in colorectal cancer; it is positively associated with visceral metastases and may affect the decision to treat with adjuvant therapy. AIMS: To evaluate whether an elastic tissue (Movat) stain facilitates i …
BACKGROUND: Venous invasion (VI) is an important prognostic factor in colorectal cancer; it is positively associated with visceral me …
A Novel Kleefstra Syndrome-associated Variant That Affects the Conserved TPLX Motif within the Ankyrin Repeat of EHMT1 Leads to Abnormal Protein Folding.
Blackburn PR, Tischer A, Zimmermann MT, Kemppainen JL, Sastry S, Knight Johnson AE, Cousin MA, Boczek NJ, Oliver G, Misra VK, Gavrilova RH, Lomberk G, Auton M, Urrutia R, Klee EW. Blackburn PR, et al. J Biol Chem. 2017 Mar 3;292(9):3866-3876. doi: 10.1074/jbc.M116.770545. Epub 2017 Jan 5. J Biol Chem. 2017. PMID: 28057753 Free PMC article.
In this report, we describe two unrelated patients with complex medical histories consistent with KS in whom next generation sequencing identified the same novel c.2426C>T (p.P809L) missense variant in EHMT1 To examine the functional significance of this novel variant, we perf …
In this report, we describe two unrelated patients with complex medical histories consistent with KS in whom next generation sequencing iden …
11 results