𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Expression of peripheral myelin protein-22 (PMP22)-mRNA in hereditary motor and sensory neuropathy type 1 (HMSN 1)

✍ Scribed by H. Grehl; T. Liehr; B. Neundörfer; B. Rautenstrauβ


Book ID
117670886
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
258 KB
Volume
7
Category
Article
ISSN
0960-8966

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Differential expression of two mRNA spec
✍ F. Bosse; G. Zoidl; S. Wilms; C. P. Gillen; H. G. Kuhn; H. W. Müller 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 988 KB

Two peripheral myelin protein PMP22 transcripts, CD25 and SR13, have been identified by Northern blot and RNA-polymerase chain reaction (PCR) methods in rat. The 0 2 5 and SR13 mRNA species (each approximately 1.8 kb in size) differ significantly in their 5'-untranslated region (5'-UTR) sequences bu

Severe Charcot-Marie-Tooth neuropathy ty
✍ Victor V. Ionasescu; Charles C. Searby; Rebecca Ionasescu; Ricardo Reisin; Victo 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB 👁 1 views

A 27-year-old man with negative family history and both parents with normal neurological evaluation and motor nerve conduction velocities (MNCVs) showed onset of severe weakness of feet at 4 years of age. Subsequently he developed left equinovarus deformity, thoracic scoliosis, ulnar nerve enlargeme

Elevated expression of messenger RNA for
✍ Dr. Hiroo Yoshikawa; Tomoya Nishimura; Yuji Nakatsuji; Harutoshi Fujimura; Masat 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 553 KB

The human peripheral myelin protein 22 (PMP-22) gene has been mapped to chromosome 1 7 ~1 1 . 2 in the duplicated region associated with Charcot-Marie-Tooth disease type 1A. Southern blot analysis using PMP-22 as a probe indicated that the PMP-22 gene was duplicated in 5 patients from unrelated Japa