✦ LIBER ✦

Analysis of amino-acid and nucleotide variants in the spinocerebellar ataxia type 1 (SCA1) gene in schizophrenic patients

✍ Scribed by Miguel Angel Pujana; Lourdes Martorell; Víctor Volpini; Joaquín Valero; Antonio Labad; Elisabet Vilella; X. Estivill

Publisher: Springer
Year: 1997
Tongue: English
Weight: 43 KB
Volume: 99
Category: Article
ISSN: 0340-6717
DOI: 10.1007/s004390050446

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Comparative studies of the CAG repeats i

Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene

✍ Limprasert, Pornprot; Nouri, Nassim; Nopparatana, Chamnong; Deininger, Prescott 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 42 KB 👁 2 views

The CAG repeat tract at the autosomal dominant spinocerebellar ataxia type 1 (SCA1) locus was analyzed in SCA1 families and French-Acadian, African-American, Caucasian, Greenland Inuit, and Thai populations. The normal alleles had 9-37 repeats, whereas disease alleles contained 44-64 repeats. The CA

Analysis of CAG repeats in SCA1, SCA2, S

Analysis of CAG repeats in SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci in spinocerebellar ataxia patients and distribution of CAG repeats at the SCA1, SCA2 and SCA6 loci in nine ethnic populations of eastern India

✍ Priyadarshi Basu; Biswanath Chattopadhyay; Prasanta K. Gangopadhaya; Subhas C. M 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 65 KB

Spinocerebellar ataxia 1 (SCA1) in the J

Spinocerebellar ataxia 1 (SCA1) in the Japanese: Analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission

✍ Yoshihiro Suzuki; Hidenao Sasaki; Akemi Wakisaka; Akio Takada; Takashi Yoshiki; 📂 Article 📅 1995 🏛 Nature Publishing Group 🌐 English ⚖ 920 KB

Analysis of the CAG repeats in the SCA1

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: Tentative association between B37 and schizophrenia

✍ Morris-Rosendahl, Deborah J.; Burgert, Edgar; Uyanik, Gökhan; Mayerova, Antonia; 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB 👁 2 views

We have genotyped unrelated French Alsatian schizophrenic and bipolar I disorder (BPD) patients and matched controls for the polymorphic CAG repeats within the genes for spinocerebellar ataxia type 1 (SCA1) and dentatorubral-pallidoluysian atrophy (B37), in order to test their possible involvement i

Abnormal activity of membrane phospholip

Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1

✍ Brian M. Ross; Klaus Eder; Anna Moszczynska; Nikolaos Mamalias; Jacques Lamarche 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 175 KB 👁 2 views

Much evidence, derived from biochemical studies of both blood and autopsied brain, has suggested that phospholipid metabolism is abnormal in patients with Friedreich's ataxia (FA), a disorder characterized by severe neuronal loss in the spinal cord and lower brain stem with no, or only modest, damag

Nucleotide and amino acid sequence varia

Nucleotide and amino acid sequence variations in the L1 open reading frame of human papillomavirus type 6

✍ Suzuki, Toshiyuki; Tomita, Yoshimi; Nagata, Hiroshi; Kono, Akiyoshi; Simizu, Bun 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 272 KB

Human papillomavirus (HPV) type 6 induces benign tumors such as condyloma acuminata and laryngeal papilloma. The HPV-6 DNA has been thought to be a heterogeneous group of subtypes and variant-types. To examine sequence variations of the HPV-6 L1 ORF, we analyzed by single-strand conformation polymor