(Q38337029)

2 September 2017

title

Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1. (English)

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2 September 2017

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17

Anne-Marie Gerdes

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2 September 2017

Malcolm Ferguson-Smith

object named as

Malcolm A Ferguson-Smith

19

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Stanley F Nelson

8

object named as

Stanley F Nelson

1 reference

2 September 2017

David R Goudie

1

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2 September 2017

Mariella D'Alessandro

2

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2 September 2017

Barry Merriman

3

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2 September 2017

Hane Lee

4

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2 September 2017

Ildikó Szeverényi

5

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2 September 2017

Stuart Avery

6

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2 September 2017

Brian D O'Connor

7

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2 September 2017

Stephanie E Coats

9

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2 September 2017

Arlene Stewart

10

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2 September 2017

Lesley Christie

11

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2 September 2017

Gabriella Pichert

12

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2 September 2017

Jean Friedel

13

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2 September 2017

Ian Hayes

14

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2 September 2017

Nigel Burrows

15

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2 September 2017

Sean Whittaker

16

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2 September 2017

Sigurd Broesby-Olsen

18

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2 September 2017

Chandra Verma

20

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2 September 2017

Declan P Lunny

21

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2 September 2017

Bruno Reversade

22

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2 September 2017

E Birgitte Lane

23

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2 September 2017

language of work or name

English

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publication date

27 February 2011

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2 September 2017

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2 September 2017

volume

43

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2 September 2017

issue

4

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2 September 2017

page(s)

365-369

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The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosity.

2 September 2017

cites work

1 reference

Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes

21 January 2018

1 reference

Multiple self-healing squamous epithelioma of Ferguson-Smith: observations in a Danish family covering four generations.

21 January 2018

1 reference

Severe exacerbation of multiple self-healing squamous epithelioma (Ferguson-Smith disease) with radiotherapy, which was successfully treated with acitretin

21 January 2018

1 reference

Multiple keratoacanthomas in a young woman: report of a case emphasizing medical management and a review of the spectrum of multiple keratoacanthomas

21 January 2018

1 reference

Ferguson Smith type multiple keratoacanthomas and a keratoacanthoma centrifugum marginatum in a woman from Japan

21 January 2018

1 reference

Transforming growth factor-beta signaling in epithelial-mesenchymal transition and progression of cancer

21 January 2018

1 reference

TGFbeta1, back to the future: revisiting its role as a transforming growth factor

21 January 2018

1 reference

Role of TGF-beta in cancer and the potential for therapy and prevention

21 January 2018

1 reference

TGFbeta1 inhibits the formation of benign skin tumors, but enhances progression to invasive spindle carcinomas in transgenic mice

21 January 2018

1 reference

Loss of TGFbeta signaling destabilizes homeostasis and promotes squamous cell carcinomas in stratified epithelia

21 January 2018

1 reference

Progressive tumor formation in mice with conditional deletion of TGF-beta signaling in head and neck epithelia is associated with activation of the PI3K/Akt pathway.

21 January 2018

1 reference

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

21 January 2018

1 reference

Recent progress in genetics of Marfan syndrome and Marfan-associated disorders

21 January 2018

1 reference

Duplication of the TGFBR1 gene causes features of Loeys-Dietz syndrome.

21 January 2018

1 reference

Aneurysm syndromes caused by mutations in the TGF-beta receptor

21 January 2018

1 reference

Mutation and cancer: statistical study of retinoblastoma

21 January 2018

1 reference

A "traffic control" role for TGFbeta3: orchestrating dermal and epidermal cell motility during wound healing

21 January 2018

1 reference

Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients

21 January 2018

1 reference

Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.

21 January 2018

1 reference

TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.

21 January 2018

1 reference

Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations.

21 January 2018

1 reference

Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.

21 January 2018

1 reference

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing

21 January 2018

1 reference

BFAST: an alignment tool for large scale genome resequencing

21 January 2018

1 reference

U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line

21 January 2018

1 reference

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

Avoiding recomputation in linkage analysis.

21 January 2018

1 reference

Ternary Complex of Transforming Growth Factor- 1 Reveals Isoform-specific Ligand Recognition and Receptor Recruitment in the Superfamily

21 January 2018

1 reference

Identification of 23TGFBR2and 6TGFBR1gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders

21 January 2018

1 reference

Phenotypic heterogeneity of Marfan-like connective tissue disorders associated with mutations in the transforming growth factor-beta receptor genes

21 January 2018

1 reference

12 December 2020

Multiple self-healing squamous epithelioma

1 reference

12 December 2020

FBN1, TGFBR1, and the Marfan-craniosynostosis/mental retardation disorders revisited.

1 reference

12 December 2020

TGFBR1*6A and cancer risk: a meta-analysis of seven case-control studies

1 reference

12 December 2020

Faster sequential genetic linkage computations

1 reference

12 December 2020

Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes

1 reference

12 December 2020

Self-healing epitheliomata of Ferguson-Smith: cytogenetic and histological studies, and the therapeutic effect of etretinate

1 reference

12 December 2020

Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry

1 reference

12 December 2020

Reversible inhibition of normal human prokeratinocyte proliferation by type beta transforming growth factor-growth inhibitor in serum-free medium

1 reference

12 December 2020

Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?

1 reference

12 December 2020

SeqWare Query Engine: storing and searching sequence data in the cloud

1 reference

12 December 2020

Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype

1 reference

12 December 2020

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Identifiers

1 reference

30 July 2022

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Dimensions Publication ID

1027823765

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Fatcat ID

release_qknjnxazrbcyvkmlnnrn6n7gam

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Fatcat

https://api.fatcat.wiki/v0/release/qknjnxazrbcyvkmlnnrn6n7gam

30 July 2022

mapped directly with Wikidata item

https://api.fatcat.wiki/v0/release/qknjnxazrbcyvkmlnnrn6n7gam

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30 July 2022