✦ LIBER ✦

The spatial distribution of fixed mutations within genes coding for proteins

✍ Scribed by Richard Holmquist; Morris Goodman; Thomas Conroy; John Czelusniak

Book ID: 105463094
Publisher: Springer
Year: 1983
Tongue: English
Weight: 983 KB
Volume: 19
Category: Article
ISSN: 0022-2844
DOI: 10.1007/bf02102319

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations affecting the structural genes

Mutations affecting the structural genes and the genes coding for modifying enzymes for ribosomal proteins in Escherichia coli

✍ Isono, Setsuko ;Isono, Katsumi ;Hirota, Yukinori 📂 Article 📅 1978 🏛 Springer 🌐 English ⚖ 605 KB

Temperature-sensitive mutants of an Escherichia coli K-12 strain PA3092 have been isolated following mutagenesis with nitrosoguanidine, and their ribosomal proteins analyzed by two-dimensional gel electrophoresis. This method was found to be very efficient in obtaining mutants with various structura

Two mutations within the coding sequence

Two mutations within the coding sequence of the phenylalanine hydroxylase gene

✍ Elisabeth Svensson; Björn Andersson; Lars Hagenfeldt 📂 Article 📅 1990 🏛 Springer 🌐 English ⚖ 645 KB

Two previously unidentified mutations at the phenylalanine hydroxylase locus were found during a study of the relationship between genotype and phenotype in phenylketonuria and hyperphenylalaninemia. One mutation eliminates the BamHI site in exon 7 and the other eliminates the HindIII site in exon 1

The structural gene coding for myelin-as

The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

✍ Dautigny, A.; Mattei, M.-G.; Morello, D.; Alliel, P. M.; Pham-Dinh, D.; Amar, L. 📂 Article 📅 1986 🏛 Nature Publishing Group 🌐 English ⚖ 383 KB

Restricted distribution of loss-of-funct

Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patients

✍ Mark V. Clough; Jeanette D. Hamlington; Iain McIntosh 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 277 KB 👁 1 views

Nail-patella syndrome (NPS) is a pleiotropic condition characterized by dysplasia of the nails, hypoplasia of the patellae, elbow dysplasia, and progressive kidney disease. The syndrome is inherited in an autosomal dominant manner and has been shown to result from mutations in the LIMhomeodomain enc

The spatial distribution of human immuno

The spatial distribution of human immunoglobulin genes within the nucleus: evidence for gene topography independent of cell type and transcriptional activity

✍ L. Parreira; Margarida Telhada; Carlos Ramos; Rosa Hernandez; Hélia Neves; Maria 📂 Article 📅 1997 🏛 Springer 🌐 English ⚖ 181 KB

A novel mutation in the β-protein coding

A novel mutation in the β-protein coding region of the amyloid β-protein precursor (APP) gene

✍ Milagros Balbín; Magnus Abrahamson; Lars Gustafson; Karin Nilsson; Arne Brun; An 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 329 KB

A novel mutation, a C to T transition at base pair 2124 in exon 17 of the amyloid beta-protein precursor (APP) gene, has been identified by direct sequencing of amplified DNA from two Alzheimer's disease (AD) patients. A simple oligonucleotide-hybridization procedure was developed to allow populatio