(Q57304636)

1

0 references

Elisabet Ars

object named as

Elisabet Ars

Xavier Estivill i Pallejà

5

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object named as

Xavier Estivill

6

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author name string

Thorsten Rosenbaum

2

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Ursula Winner

4

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Conxi Lázaro

https://scigraph.springernature.com/pub.10.1038/90148

7

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language of work or name

English

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publication date

July 2001

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published in

Nature Genetics

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volume

28

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page(s)

294-296

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issue

3

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exact match

0 references

cites work

Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations

1 reference

7 January 2021

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

1 reference

7 January 2021

Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene

1 reference

7 January 2021

Confirmation of a double-hit model for the NF1 gene in benign neurofibromas

1 reference

7 January 2021

Allelic loss of the NF1 gene in NF1-associated plexiform neurofibromas

1 reference

7 January 2021

Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.

1 reference

7 January 2021

A search for evidence of somatic mutations in the NF1 gene.

1 reference

7 January 2021

Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1

1 reference

7 January 2021

Somatic NF1 mutational spectrum in benign neurofibromas: mRNA splice defects are common among point mutations

1 reference

7 January 2021

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences.

1 reference

7 January 2021

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1 reference

7 January 2021

Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination

1 reference

7 January 2021

Culture of cytogenetically abnormal schwann cells from benign and malignant NF1 tumors

1 reference

7 January 2021

Unequal meiotic crossover: a frequent cause of NF1 microdeletions.

1 reference

7 January 2021

Interindividual variation in mitotic recombination

1 reference

7 January 2021

Cancer predisposition caused by elevated mitotic recombination in Bloom mice

1 reference

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

7 January 2021

A simple, rapid method for isolation of high quality genomic DNA from animal tissues

1 reference

7 January 2021

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

1 reference

7 January 2021

Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.

1 reference

7 January 2021