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8 in total

1. Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols.

Authors: M Angers; J F Cloutier; A Castonguay; R Drouin
Journal: Nucleic Acids Res Date: 2001-08-15 Impact factor: 16.971

2. Two-step cycle sequencing improves base ambiguities and signal dropouts in DNA sequencing reactions using energy-transfer-based fluorescent dye terminators.

Authors: L Wen
Journal: Mol Biotechnol Date: 2001-02 Impact factor: 2.695

3. Betaine improves the PCR amplification of GC-rich DNA sequences.

Authors: W Henke; K Herdel; K Jung; D Schnorr; S A Loening
Journal: Nucleic Acids Res Date: 1997-10-01 Impact factor: 16.971

4. A fundamental study of the PCR amplification of GC-rich DNA templates.

Authors: T G Mamedov; E Pienaar; S E Whitney; J R TerMaat; G Carvill; R Goliath; A Subramanian; H J Viljoen
Journal: Comput Biol Chem Date: 2008-07-25 Impact factor: 2.877

5. A mammalian adaptor protein with conserved Src homology 2 and phosphotyrosine-binding domains is related to Shc and is specifically expressed in the brain.

Authors: J P O'Bryan; Z Songyang; L Cantley; C J Der; T Pawson
Journal: Proc Natl Acad Sci U S A Date: 1996-04-02 Impact factor: 11.205

Use of deoxyinosine in PCR to improve amplification of GC-rich DNA.

1. Optimal conditions to use Pfu exo(-) DNA polymerase for highly efficient ligation-mediated polymerase chain reaction protocols.

2. Two-step cycle sequencing improves base ambiguities and signal dropouts in DNA sequencing reactions using energy-transfer-based fluorescent dye terminators.

3. Betaine improves the PCR amplification of GC-rich DNA sequences.

4. A fundamental study of the PCR amplification of GC-rich DNA templates.

5. A mammalian adaptor protein with conserved Src homology 2 and phosphotyrosine-binding domains is related to Shc and is specifically expressed in the brain.

6. Betaine, dimethyl sulfoxide, and 7-deaza-dGTP, a powerful mixture for amplification of GC-rich DNA sequences.

7. Molecular cloning and expression of high GC-rich novel tumor suppressor gene HIC-1.

8. Polymerase chain reaction amplification of a GC rich region by adding 1,2 propanediol.