(Q28214767)

7

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author name string

K Grohmann

1

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M Schuelke

2

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A Diers

3

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K Hoffmann

4

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B Lucke

5

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C Adams

6

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H Leonhardt-Horti

8

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F Muntoni

9

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R Ouvrier

10

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A Pfeufer

11

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R Rossi

12

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L Van Maldergem

13

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J M Wilmshurst

14

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T F Wienker

15

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S Rudnik-Schöneborn

17

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K Zerres

18

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C Hübner

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

19

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language of work or name

English

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publication date

September 2001

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published in

Nature Genetics

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volume

29

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issue

1

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page(s)

75-7

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cites work

1 reference

7 January 2021

The role of the SMN gene in proximal spinal muscular atrophy

1 reference

7 January 2021

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems

1 reference

7 January 2021

Identification of survival motor neuron as a transcriptional activator-binding protein.

1 reference

7 January 2021

Direct interaction of Smn with dp103, a putative RNA helicase: a role for Smn in transcription regulation?

1 reference

7 January 2021

Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins

1 reference

7 January 2021

Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy

1 reference

7 January 2021

A functional interaction between the survival motor neuron complex and RNA polymerase II

1 reference

7 January 2021

Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: A variant of infantile spinal muscular atrophy

1 reference

7 January 2021

Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings.

1 reference

7 January 2021

Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.

1 reference

7 January 2021

59th ENMC International Workshop: Spinal Muscular Atrophies: recent progress and revised diagnostic criteria 17-19 April 1998, Soestduinen, The Netherlands.

1 reference

7 January 2021

Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele

1 reference

7 January 2021

Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration

1 reference

7 January 2021

Evidence for regulation of transcription and replication of the human neurotropic virus JCV genome by the human S(mu)bp-2 protein in glial cells

1 reference

7 January 2021

Association of the mammalian helicase MAH with the pre-mRNA splicing complex

1 reference

7 January 2021

Smubp-2 represses the Epstein-Barr virus lytic switch promoter

1 reference

7 January 2021

The rat ortholog of the presumptive flounder antifreeze enhancer-binding protein is a helicase domain-containing protein.

1 reference

7 January 2021

Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14.

1 reference

7 January 2021

Severe infantile axonal neuropathy with respiratory failure

1 reference

7 January 2021

Isolation of cDNA encoding a binding protein specific to 5'-phosphorylated single-stranded DNA with G-rich sequences

1 reference

7 January 2021

The R3H motif: a domain that binds single-stranded nucleic acids

1 reference

7 January 2021

The domain encoded by exon 2 of the survival motor neuron protein mediates nucleic acid binding.

1 reference

7 January 2021

Characterization of DP103, a novel DEAD box protein that binds to the Epstein-Barr virus nuclear proteins EBNA2 and EBNA3C

1 reference

7 January 2021