Single-base sequencing for rapid screening of plasmids for inserts with known mutations and correct orientation

Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants.

Molecular genetics and metabolism·2008

4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?

Kidney international·2006

Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutations.

Molecular genetics and metabolism·2006

Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria.

Molecular genetics and metabolism·2001

Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).

Molecular genetics and metabolism·2001

Identification of the first reported splice site mutation (IVS7-1G-->A) in the aminomethyltransferase (T-protein) gene (AMT) of the glycine cleavage complex in 3 unrelated families with nonketotic hyperglycinemia.

Human mutation·2001

Detection of antisense oligonucleotides from biological samples by ligase detection reaction using T4 RNA ligase 2.

BioTechniques·2026

A PCR method to detect the mouse major histocompatibility complex H2-Ld gene that confers resistance to Toxoplasma encephalitis.

BioTechniques·2026

Investigating the interactomic landscape of survival motor neuron (SMN) and the SMNΔ7 truncated protein.

BioTechniques·2026

Antigen retrieval-immunofluorescence on free floating sections to visualize the liver lobule and its cellular makeup.

BioTechniques·2026

Special approach of droplet digital polymerase chain reaction (ddPCR) for transgene stability of a Chinese hamster ovary (CHO) cell line.

BioTechniques·2026

Strand-specific quantification of L1 ORF0 and related transcripts by multiplex reverse transcription with tagged primers.

BioTechniques·2026

Detection of the Novel HLA-A*01:522 Allele by Next-Generation Sequencing in a Brazilian Individual.

HLA·2026

Parental haplotype reconstruction in up to 440,209 UK and Estonian individuals reveals recent assortative mating dynamics.

Nature human behaviour·2026

Characterisation of HLA-C*12:118:02 in a Brazilian Volunteer Bone Marrow Donor.

HLA·2026

Viral Nuclease Inhibitors: Small molecule disruptors of the UL12 alkaline nuclease display broad anti-herpes virus activity.

PLoS pathogens·2026

Over-Representation of Sperm-Associated Deleterious Mutations Across Wild and Ex Situ Cheetah (Acinonyx jubatus) Populations.

Molecular ecology·2026

Predictive models of the genetic bases underlying budding yeast fitness in multiple environments.

NAR genomics and bioinformatics·2026

Related Experiment Videos

Single-base sequencing for rapid screening of plasmids for inserts with known mutations and correct orientation

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Partial trypsin digestion as an indicator of mis-folding of mutant alanine:glyoxylate aminotransferase and chaperone effects of specific ligands. Study of a spectrum of missense mutants.

4-Hydroxyproline metabolism and glyoxylate production: A target for substrate depletion in primary hyperoxaluria?

Consequences of missense mutations for dimerization and turnover of alanine:glyoxylate aminotransferase: study of a spectrum of mutations.

Three novel deletions in the alanine:glyoxylate aminotransferase gene of three patients with type 1 hyperoxaluria.

Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N145I): a strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH).

Identification of the first reported splice site mutation (IVS7-1G-->A) in the aminomethyltransferase (T-protein) gene (AMT) of the glycine cleavage complex in 3 unrelated families with nonketotic hyperglycinemia.

Detection of antisense oligonucleotides from biological samples by ligase detection reaction using T4 RNA ligase 2.

A PCR method to detect the mouse major histocompatibility complex H2-Ld gene that confers resistance to Toxoplasma encephalitis.

Investigating the interactomic landscape of survival motor neuron (SMN) and the SMNΔ7 truncated protein.

Antigen retrieval-immunofluorescence on free floating sections to visualize the liver lobule and its cellular makeup.

Special approach of droplet digital polymerase chain reaction (ddPCR) for transgene stability of a Chinese hamster ovary (CHO) cell line.

Strand-specific quantification of L1 ORF0 and related transcripts by multiplex reverse transcription with tagged primers.

Detection of the Novel HLA-A*01:522 Allele by Next-Generation Sequencing in a Brazilian Individual.

Parental haplotype reconstruction in up to 440,209 UK and Estonian individuals reveals recent assortative mating dynamics.

Characterisation of HLA-C*12:118:02 in a Brazilian Volunteer Bone Marrow Donor.

Viral Nuclease Inhibitors: Small molecule disruptors of the UL12 alkaline nuclease display broad anti-herpes virus activity.

Over-Representation of Sperm-Associated Deleterious Mutations Across Wild and Ex Situ Cheetah (Acinonyx jubatus) Populations.

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Single-base sequencing for rapid screening of plasmids for inserts with known mutations and correct orientation

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