These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
44 related articles for article (PubMed ID: 36044908)
1. Pathogenic postzygotic mosaicism in the tyrosine receptor kinase pathway: potential unidentified human disease hidden away in a few cells. Tiemann-Boege I; Mair T; Yasari A; Zurovec M FEBS J; 2021 May; 288(10):3108-3119. PubMed ID: 32810928 [TBL] [Abstract][Full Text] [Related]
2. Genomic Mosaicism of the Brain: Origin, Impact, and Utility. Graham JH; Schlachetzki JCM; Yang X; Breuss MW Neurosci Bull; 2024 Jun; 40(6):759-776. PubMed ID: 37898991 [TBL] [Abstract][Full Text] [Related]
3. Human embryonic genetic mosaicism and its effects on development and disease. Waldvogel SM; Posey JE; Goodell MA Nat Rev Genet; 2024 Apr; ():. PubMed ID: 38605218 [TBL] [Abstract][Full Text] [Related]
4. Building the brain mosaic: an expanded view. Sran S; Ringland A; Bedrosian TA Trends Genet; 2024 Sep; 40(9):747-756. PubMed ID: 38853120 [TBL] [Abstract][Full Text] [Related]
5. Shikonin reactivates TSGs GADD45B and PPP3CC to block NSCLC cell proliferation and migration through JNK/P38/MAPK signaling pathways. Zhao Y; Wu D; Fu Z; Liu W; Yao Y; Liang Y BMC Complement Med Ther; 2024 Jan; 24(1):10. PubMed ID: 38167059 [TBL] [Abstract][Full Text] [Related]
6. Comprehensive genetic and phenotype analysis of 95 individuals with mosaic tuberous sclerosis complex. Klonowska K; Giannikou K; Grevelink JM; Boeszoermenyi B; Thorner AR; Herbert ZT; Afrin A; Treichel AM; Hamieh L; Kotulska K; Jozwiak S; Moss J; Darling TN; Kwiatkowski DJ Am J Hum Genet; 2023 Jun; 110(6):979-988. PubMed ID: 37141891 [TBL] [Abstract][Full Text] [Related]
7. Unexpected Findings in Hereditary Breast and Ovarian Cancer Syndrome: Low-Level Constitutional Mosaicism in Hidalgo Mayoral I; Almeida Santiago A; Sánchez-Zapardiel JM; Hidalgo Calero B; de la Hoya M; Gómez-Sanz A; de Miguel Reyes M; Robles L Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833429 [TBL] [Abstract][Full Text] [Related]
8. Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes? Kehrer-Sawatzki H; Cooper DN J Med Genet; 2008 Oct; 45(10):622-31. PubMed ID: 18511569 [TBL] [Abstract][Full Text] [Related]
9. Genetics, genomics, and genotype-phenotype correlations of TSC: Insights for clinical practice. Peron A; Au KS; Northrup H Am J Med Genet C Semin Med Genet; 2018 Sep; 178(3):281-290. PubMed ID: 30255984 [TBL] [Abstract][Full Text] [Related]
10. Mosaicism in Tumor Suppressor Gene Syndromes: Prevalence, Diagnostic Strategies, and Transmission Risk. Chen JL; Miller DT; Schmidt LS; Malkin D; Korf BR; Eng C; Kwiatkowski DJ; Giannikou K Annu Rev Genomics Hum Genet; 2022 Aug; 23():331-361. PubMed ID: 36044908 [TBL] [Abstract][Full Text] [Related]
11. Low-level mosaicism in tuberous sclerosis complex: prevalence, clinical features, and risk of disease transmission. Giannikou K; Lasseter KD; Grevelink JM; Tyburczy ME; Dies KA; Zhu Z; Hamieh L; Wollison BM; Thorner AR; Ruoss SJ; Thiele EA; Sahin M; Kwiatkowski DJ Genet Med; 2019 Nov; 21(11):2639-2643. PubMed ID: 31160751 [TBL] [Abstract][Full Text] [Related]
12. Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. Kim SH; Kwon SS; Park MR; Lee HA; Kim JH; Cha J; Kim S; Baek ST; Kim SH; Lee JS; Kim HD; Choi JR; Lee ST; Kang HC J Mol Diagn; 2023 Aug; 25(8):583-591. PubMed ID: 37088138 [TBL] [Abstract][Full Text] [Related]
13. Ultra deep sequencing detects a low rate of mosaic mutations in tuberous sclerosis complex. Qin W; Kozlowski P; Taillon BE; Bouffard P; Holmes AJ; Janne P; Camposano S; Thiele E; Franz D; Kwiatkowski DJ Hum Genet; 2010 Mar; 127(5):573-82. PubMed ID: 20165957 [TBL] [Abstract][Full Text] [Related]
14. Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing. Tyburczy ME; Dies KA; Glass J; Camposano S; Chekaluk Y; Thorner AR; Lin L; Krueger D; Franz DN; Thiele EA; Sahin M; Kwiatkowski DJ PLoS Genet; 2015 Nov; 11(11):e1005637. PubMed ID: 26540169 [TBL] [Abstract][Full Text] [Related]
15. Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations. Kozlowski P; Roberts P; Dabora S; Franz D; Bissler J; Northrup H; Au KS; Lazarus R; Domanska-Pakiela D; Kotulska K; Jozwiak S; Kwiatkowski DJ Hum Genet; 2007 May; 121(3-4):389-400. PubMed ID: 17287951 [TBL] [Abstract][Full Text] [Related]