105 related articles for article (PubMed ID: 18786629)
1. Analysis of human disease genes in the context of gene essentiality.
Park D; Park J; Park SG; Park T; Choi SS
Genomics; 2008 Dec; 92(6):414-8. PubMed ID: 18786629
[TBL] [Abstract][Full Text] [Related]
2. Interpreting neonatal lethal phenotypes in mouse mutants: insights into gene function and human diseases.
Turgeon B; Meloche S
Physiol Rev; 2009 Jan; 89(1):1-26. PubMed ID: 19126753
[TBL] [Abstract][Full Text] [Related]
3. The complex relationship of gene duplication and essentiality.
Makino T; Hokamp K; McLysaght A
Trends Genet; 2009 Apr; 25(4):152-5. PubMed ID: 19285746
[TBL] [Abstract][Full Text] [Related]
4. An essential gene mutagenesis screen across the highly conserved piebald deletion region of mouse chromosome 14.
Hagarman JA; O'Brien TP
Genesis; 2009 Jun; 47(6):392-403. PubMed ID: 19391113
[TBL] [Abstract][Full Text] [Related]
5. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
6. Single mutation at the amino acid position 627 of PB2 that leads to increased virulence of an H5N1 avian influenza virus during adaptation in mice can be compensated by multiple mutations at other sites of PB2.
Li J; Ishaq M; Prudence M; Xi X; Hu T; Liu Q; Guo D
Virus Res; 2009 Sep; 144(1-2):123-9. PubMed ID: 19393699
[TBL] [Abstract][Full Text] [Related]
7. Physicochemical property changes of amino acid residues that accompany missense mutations in SCN1A affect epilepsy phenotype severity.
Kanai K; Yoshida S; Hirose S; Oguni H; Kuwabara S; Sawai S; Hiraga A; Fukuma G; Iwasa H; Kojima T; Kaneko S
J Med Genet; 2009 Oct; 46(10):671-9. PubMed ID: 19586930
[TBL] [Abstract][Full Text] [Related]
8. Human herpesvirus 6 ganciclovir-resistant strain with amino acid substitutions associated with the death of an allogeneic stem cell transplant recipient.
Isegawa Y; Hara J; Amo K; Osugi Y; Takemoto M; Yamanishi K; Fukunaga R; Shibata M; Ohshima A; Horiguchi Y; Sugimoto N
J Clin Virol; 2009 Jan; 44(1):15-9. PubMed ID: 18952495
[TBL] [Abstract][Full Text] [Related]
9. Pathogenic or not? And if so, then how? Studying the effects of missense mutations using bioinformatics methods.
Thusberg J; Vihinen M
Hum Mutat; 2009 May; 30(5):703-14. PubMed ID: 19267389
[TBL] [Abstract][Full Text] [Related]
10. Incorporating the amino acid properties to predict the significance of missense mutations.
Lee TC; Lee AS; Li KB
Amino Acids; 2008 Oct; 35(3):615-26. PubMed ID: 18415037
[TBL] [Abstract][Full Text] [Related]
11. Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects.
Korstanje R; Desai J; Lazar G; King B; Rollins J; Spurr M; Joseph J; Kadambi S; Li Y; Cherry A; Matteson PG; Paigen B; Millonig JH
Physiol Genomics; 2008 Nov; 35(3):296-304. PubMed ID: 18796533
[TBL] [Abstract][Full Text] [Related]
12. Spatiotemporal distribution of Fras1/Frem proteins during mouse embryonic development.
Chiotaki R; Petrou P; Giakoumaki E; Pavlakis E; Sitaru C; Chalepakis G
Gene Expr Patterns; 2007 Feb; 7(4):381-8. PubMed ID: 17251066
[TBL] [Abstract][Full Text] [Related]
13. [Genes controlling ontogenesis: morphosis, phenocopies, dimorphs, and other visible expressions of mutant genes].
Chadov BF; Chadova EV; Kopyl SA; Khotskina EA; Fedorova NB
Genetika; 2004 Mar; 40(3):353-65. PubMed ID: 15125250
[TBL] [Abstract][Full Text] [Related]
14. Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency.
Monnot S; Serre V; Chadefaux-Vekemans B; Aupetit J; Romano S; De Lonlay P; Rival JM; Munnich A; Steffann J; Bonnefont JP
Hum Mutat; 2009 May; 30(5):734-40. PubMed ID: 19306334
[TBL] [Abstract][Full Text] [Related]
15. Comparative genomics and the study of evolution by natural selection.
Ellegren H
Mol Ecol; 2008 Nov; 17(21):4586-96. PubMed ID: 19140982
[TBL] [Abstract][Full Text] [Related]
16. The neurofilament light chain gene (NEFL) mutation Pro22Ser can be associated with mixed axonal and demyelinating neuropathy.
Bhagavati S; Maccabee PJ; Xu W
J Clin Neurosci; 2009 Jun; 16(6):830-1. PubMed ID: 19286384
[TBL] [Abstract][Full Text] [Related]
17. Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Law LK; Tang NL; Hui J; Fung SL; Ruiter J; Wanders RJ; Fok TF; Lam CW
Clin Chim Acta; 2009 Jun; 404(2):95-9. PubMed ID: 19265687
[TBL] [Abstract][Full Text] [Related]
18. Consequences of mutations within the C terminus of the FHL1 gene.
Schoser B; Goebel HH; Janisch I; Quasthoff S; Rother J; Bergmann M; Müller-Felber W; Windpassinger C
Neurology; 2009 Aug; 73(7):543-51. PubMed ID: 19687455
[TBL] [Abstract][Full Text] [Related]
19. Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: description of novel mutations and novel genotype-phenotype correlations.
Zenteno JC; Correa-Gomez V; Santacruz-Valdez C; Suarez-Sanchez R; Villanueva-Mendoza C
Exp Eye Res; 2009 Aug; 89(2):172-7. PubMed ID: 19303004
[TBL] [Abstract][Full Text] [Related]
20. Functional analysis of HNPCC-related missense mutations in MSH2.
Lützen A; de Wind N; Georgijevic D; Nielsen FC; Rasmussen LJ
Mutat Res; 2008 Oct; 645(1-2):44-55. PubMed ID: 18822302
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
