(Q28282762)

T Meitinger

19

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Katherine L Dry

K Dry

2

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Alfons Meindl

1

A Meindl

0 references

Eberhart Zrenner

13

E Zrenner

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author name string

K Herrmann

3

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A Ciccodicola

5

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A Edgar

6

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M R Carvalho

7

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H Achatz

8

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H Hellebrand

9

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A Lennon

10

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C Migliaccio

11

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K Porter

12

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A Bird

14

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M Jay

15

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B Lorenz

16

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B Wittwer

17

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M D'Urso

18

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A Wright

https://scigraph.springernature.com/pub.10.1038/ng0596-35

20

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language of work or name

English

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publication date

May 1996

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published in

Nature Genetics

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volume

13

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page(s)

35-42

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issue

1

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exact match

0 references

cites work

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

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Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

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Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families.

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Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families

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Identification of a gene from Xp21 with similarity to the tctex-1 gene of the murine t complex

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Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype

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A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

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Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3).

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Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

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Chromosomal assignments of 3'-directed partial cDNA sequences representing novel genes expressed in granulocytoid cells

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A human RNase E-like activity that cleaves RNA sequences involved in mRNA stability control

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RCC1 in the cell cycle: the regulator of chromosome condensation takes on new roles

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Isolation and characterization of the active cDNA of the human cell cycle gene (RCC1) involved in the regulation of onset of chromosome condensation

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Cloning of Xenopus RCC1 cDNA, a homolog of the human RCC1 gene: complementation of tsBN2 mutation and identification of the product.

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Protein translocation: nuclear export--out of the dark

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Protein kinase recognition sequence motifs

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Complete nucleotide sequence of the human RCC1 gene involved in coupling between DNA replication and mitosis

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Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome

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Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

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Catalysis of guanine nucleotide exchange on Ran by the mitotic regulator RCC1

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Crystal structure of the nuclear Ras-related protein Ran in its GDP-bound form.

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Diverse effects of the guanine nucleotide exchange factor RCC1 on RNA transport

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The Ran/TC4 GTPase-binding domain: identification by expression cloning and characterization of a conserved sequence motif

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The RCC1 protein interacts with Ran, RanBP1, hsc70, and a 340-kDa protein in Xenopus extracts.

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Tissue-specific expression of Ran isoforms in the mouse

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Retinal degeneration in choroideremia: deficiency of rab geranylgeranyl transferase

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Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries

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Improved tools for biological sequence comparison

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