(Q28294011)

16

0 references

Marie-Germaine Bousser

18

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Anne Ducros

A Ducros

3

0 references

Anne Joutel

A Joutel

Elisabeth Tournier-Lasserve

1

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E Tournier-Lasserve

19

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M M Ruchoux

15

M M Ruchoux

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author name string

C Corpechot

2

0 references

K Vahedi

4

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H Chabriat

5

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P Mouton

6

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S Alamowitch

7

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V Domenga

8

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M Cécillion

9

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E Marechal

10

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J Maciazek

11

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C Vayssiere

12

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E A Cabanis

14

0 references

J F Bach

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy

17

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language of work or name

English

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publication date

24 October 1996

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published in

Nature

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volume

383

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issue

6602

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page(s)

707-10

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cites work

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7 January 2021

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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7 January 2021

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

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Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

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7 January 2021

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

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7 January 2021

A transcription map of the region containing the Huntington disease gene

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7 January 2021

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments

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7 January 2021

The novel Notch homologue mouse Notch 3 lacks specific epidermal growth factor-repeats and is expressed in proliferating neuroepithelium

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7 January 2021

The Human NOTCH1, 2, and 3 Genes Are Located at Chromosome Positions 9q34, 1p13-p11, and 19p13.2-p13.1 in Regions of Neoplasia-Associated Translocation

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7 January 2021

Nucleotide sequence from the neurogenic locus notch implies a gene product that shares homology with proteins containing EGF-like repeats

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7 January 2021

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TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms

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7 January 2021

Human homologs of a Drosophila Enhancer of split gene product define a novel family of nuclear proteins

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7 January 2021

Structure and distribution of the Notch protein in developing Drosophila.

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7 January 2021

Specific EGF repeats of Notch mediate interactions with Delta and serrate: Implications for notch as a multifunctional receptor

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7 January 2021

The maternal genes apx-1 and glp-1 and establishment of dorsal-ventral polarity in the early C. elegans embryo

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7 January 2021

The suppressor of hairless protein participates in notch receptor signaling

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7 January 2021

Jagged: A mammalian ligand that activates notch1

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7 January 2021

Isolation and expression of scabrous, a gene regulating neurogenesis in Drosophila

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7 January 2021

Facilitation of lin-12-mediated signalling by sel-12, a Caenorhabditis elegans S182 Alzheimer's disease gene

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7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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7 January 2021

Epidermal growth factor-like modules

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7 January 2021

Specific truncations of Drosophila Notch define dominant activated and dominant negative forms of the receptor.

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7 January 2021

Mutations altering the structure of epidermal growth factor-like coding sequences at the Drosophila Notch locus

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7 January 2021

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

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7 January 2021

A hypervariable region at the D19S11 locus

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7 January 2021

The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression

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7 January 2021

An integrated metric physical map of human chromosome 19.

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7 January 2021