✦ LIBER ✦

The molecular characterization of an A:T to G:C transition in theHbb-b1gene of the murine homologue of hemoglobin Rainier

✍ Scribed by Janet Jones; Josephine Peters

Book ID: 105569577
Publisher: Springer
Year: 1991
Tongue: English
Weight: 529 KB
Volume: 29
Category: Article
ISSN: 0006-2928
DOI: 10.1007/bf02426875

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The molecular characterization of an A:T

The molecular characterization of an A:T to G:C transition in theHbb-b1gene of the murine homologue of hemoglobin Rainier

✍ Janet Jones,Josephine Peters 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 529 KB

Hemoglobin M Iwate is caused by a C→T tr

Hemoglobin M Iwate is caused by a C→T transition in codon 87 of the human α1-globin gene

✍ J. Horst; G. Assum; E. U. Griese; A. Eigel; W. Hampl; E. Kohne 📂 Article 📅 1987 🏛 Springer 🌐 English ⚖ 473 KB

DNA restriction, molecular cloning, and sequencing methods have been used to characterize the mutation leading to the methemoglobinemia HbM Iwate. It could be demonstrated that the HbM Iwate defect is caused by a point mutation involving a transition from C to T in the first position of codon 87 of

C to T transition at the first nucleotid

C to T transition at the first nucleotide of codon 63 of the β-globin gene corresponding to hemoglobin M-Saskatoon in an Indonesian boy

✍ Purnomo Suryantoro; Yasuhiro Takeshima; Alimsardjono Haryanto; Masafumi Matsuo 📂 Article 📅 1995 🏛 Nature Publishing Group 🌐 English ⚖ 476 KB

Induction of A:T to G:C transition mutat

Induction of A:T to G:C transition mutations by 5-(2-chloroethyl)-2′-deoxyuridine (CEDU), an antiviral pyrimidine nucleoside analogue, in the bone marrow of Muta™Mouse

✍ Frank Staedtler; Willi Suter; Hans-Joerg Martus 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 176 KB

Molecular characterization of the murine

Molecular characterization of the murine SIGNR1 gene encoding a C-type lectin homologous to human DC-SIGN and DC-SIGNR

✍ Stephen A Parent; Theresa Zhang; Gary Chrebet; Joseph A Clemas; David J Figueroa 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 680 KB

GγAγ(β+) hereditary persistence of fetal

GγAγ(β+) hereditary persistence of fetal hemoglobin: The Gγ – 158 C → T mutation in cis to the − 175 T → C mutation of the Aγ-globin gene results in increased Gγ-globin synthesis

✍ M. B. Coleman; J. G. Adams III; M. H. Steinberg; M. W. Plonczynski; A. H. Harrel 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 483 KB 👁 1 views