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Human Mutation
Results: 293

#	Item
261	Exploring the gonad transcriptome of two extreme male pigs with RNA-seq Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Genomics Genetic mapping Mobile genetic elements Genome Mutation Retrotransposon Human genome Transposable element DNA Biology Genetics Molecular biology
262	Exploring the gonad transcriptome of two extreme male pigs with RNA-seq Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Molecular genetics Mutation Genomics Evolution by Gene Duplication Gene duplication Human genome Fis Copy-number variation Subfunctionalization Biology Genetics Molecular evolution
263	Modeling Effects of Human Single Nucleotide Polymorphisms on Protein-Protein Interactions Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Molecular biology Mutation Bioinformatics Chemical bonding Protein domain Salt bridge Point mutation Amino acid Synonymous substitution Biology Chemistry Protein structure
264	O਒ਉਇਉ਎ਁ਌ A਒ਔਉਃ਌ਅ The AQP1 mutation c.601delG causes the Co-negative phenotype in four patients belonging to the Romani (Gypsy) ethnic group Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Transfusion medicine Genetics Hematology Molecular biology Null allele Rh blood group system Blood type Colton antigen system Human blood group systems Biology Anatomy Blood
265	NIH Public Access Author Manuscript Science. Author manuscript; available in PMC 2011 April 29. Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Copy-number variation Segmental duplication Genomes Project Representation oligonucleotide microarray analysis Gene duplication Human genome Genome Gene Mutation Biology Genetics Philosophy of biology
266	CpGPAP: CpG island predictor analysis platform Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English DNA Genetic genealogy Mitochondrial genetics Heteroplasmy Deafness Homoplasmy Mitochondrial disease Mitochondrial DNA Human mitochondrial genetics Genetics Biology Mutation
267	Case report Congenital analbuminemia caused by a novel aberrant splicing in the albumin gene Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English RNA splicing Spliceosome DNA Blood proteins Human serum albumin Exon Mutation Complementary DNA Splice site mutation Biology Genetics Gene expression
268	Am. J. Hum. Genet. 65:1261–1267, 1999 The g-Crystallins and Human Cataracts: A Puzzle Made Clearer Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English CRYGC Cataract Molecular biology Alpha crystallin Crystallin Point mutation Mutation Lens Pseudogene Biology Genetics Protein families
269	Human Molecular Genetics, 2003, Vol. 12, No. 21 DOI: [removed]hmg/ddg306 Add to Reading List Source URL: hmg.oxfordjournals.org Language: English Genodermatoses Rare diseases Syndromes RECQL4 Rothmund–Thomson syndrome RecQ helicase Werner syndrome ATP-dependent helicase Mutation Molecular genetics Health Genetics Biology
270	doi:[removed]j.tree[removed] Add to Reading List Source URL: www.zoology.wisc.edu Language: English - Date: 2007-03-15 15:20:49 Molecular evolution Mutation Molecular biology Ka/Ks ratio Adaptive evolution in the human genome Neutral theory of molecular evolution McDonald–Kreitman test Mutation rate Neutral mutation Biology Evolutionary biology Genetics

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