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17 in total

1. Segmental duplications in euchromatic regions of human chromosome 5: a source of evolutionary instability and transcriptional innovation.

Authors: Anouk Courseaux; Florence Richard; Josiane Grosgeorge; Christine Ortola; Agnes Viale; Claude Turc-Carel; Bernard Dutrillaux; Patrick Gaudray; Jean-Louis Nahon
Journal: Genome Res Date: 2003-03 Impact factor: 9.043

2. Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos.

Authors: B Schrank; R Götz; J M Gunnersen; J M Ure; K V Toyka; A G Smith; M Sendtner
Journal: Proc Natl Acad Sci U S A Date: 1997-09-02 Impact factor: 11.205

3. The CD28/CTLA-4:B7 receptor system in experimental autoimmune encephalomyelitis.

Authors: P S Linsley
Journal: J Clin Invest Date: 1995-06 Impact factor: 14.808

4. Distinct roles of yeast MEC and RAD checkpoint genes in transcriptional induction after DNA damage and implications for function.

Authors: G L Kiser; T A Weinert
Journal: Mol Biol Cell Date: 1996-05 Impact factor: 4.138

5. Gene deletions in spinal muscular atrophy.

Authors: N R Rodrigues; N Owen; K Talbot; S Patel; F Muntoni; J Ignatius; V Dubowitz; K E Davies
Journal: J Med Genet Date: 1996-02 Impact factor: 6.318

6. Heterogeneity of subcellular localization and electrophoretic mobility of survival motor neuron (SMN) protein in mammalian neural cells and tissues.

Authors: J W Francis; A W Sandrock; P G Bhide; J P Vonsattel; R H Brown
Journal: Proc Natl Acad Sci U S A Date: 1998-05-26 Impact factor: 11.205

7. Epstein-Barr virus vectors for gene delivery to B lymphocytes.

Authors: E S Robertson; T Ooka; E D Kieff
Journal: Proc Natl Acad Sci U S A Date: 1996-10-15 Impact factor: 11.205

8. New, Improved Version of the mCOP-PCR Screening System for Detection of Spinal Muscular Atrophy Gene (SMN1) Deletion.

Authors: Masakazu Shinohara; Mawaddah Ar Rochmah; Kenta Nakanishi; Nur Imma Fatimah Harahap; Emma Tabe Eko Niba; Toshio Saito; Kayoko Saito; Atsuko Takeuchi; Yoshihiro Bouike; Hisahide Nishio
Journal: Kobe J Med Sci Date: 2017-09-07

9. Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel.

Authors: N Mitrović; A L George; H Lerche; S Wagner; C Fahlke; F Lehmann-Horn
Journal: J Physiol Date: 1995-08-15 Impact factor: 5.182

10. Molecular diagnosis of spinal muscular atrophy.

Authors: H Stewart; A Wallace; J McGaughran; R Mountford; H Kingston
Journal: Arch Dis Child Date: 1998-06 Impact factor: 3.791