(Q24323110)

intermediate filament organization

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Manabu Ohyama

5

0 references

Junken Aoki

object named as

Junken Aoki

10

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author name string

Atsushi Fujimoto

1

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Muhammad Farooq

2

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Hiroki Fujikawa

3

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Asuka Inoue

4

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Ritsuko Ehama

6

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Jotaro Nakanishi

7

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Motofumi Hagihara

8

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Tokuro Iwabuchi

9

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Masaaki Ito

11

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Yutaka Shimomura

Journal of Investigative Dermatology

12

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language of work or name

English

0 references

publication date

October 2012

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published in

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volume

132

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issue

10

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page(s)

2342-9

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cites work

A novel type II cytokeratin, mK6irs, is expressed in the Huxley and Henle layers of the mouse inner root sheath

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Unveiling the roots of monogenic genodermatoses: genotrichoses as a paradigm

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Coat variation in the domestic dog is governed by variants in three genes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Hereditary woolly hair and keratosis pilaris

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

'Hard' and 'soft' principles defining the structure, function and regulation of keratin intermediate filaments

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

LPA-producing enzyme PA-PLA₁α regulates hair follicle development by modulating EGFR signalling

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Pathogenesis of monilethrix: computer stereography and electron microscopy

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Identification of the rat Rex mutation as a 7-bp deletion at splicing acceptor site of the Krt71 gene.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

A novel epithelial keratin, hK6irs1, is expressed differentially in all layers of the inner root sheath, including specialized huxley cells (Flügelzellen) of the human hair follicle

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

K6irs1, K6irs2, K6irs3, and K6irs4 represent the inner-root-sheath-specific type II epithelial keratins of the human hair follicle

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

The mouse waved-2 phenotype results from a point mutation in the EGF receptor tyrosine kinase

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mice with a null mutation of the TGF alpha gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

The human keratins: biology and pathology

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Efficient selection for high-expression transfectants with a novel eukaryotic vector

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Identification of p2y9/GPR23 as a Novel G Protein-coupled Receptor for Lysophosphatidic Acid, Structurally Distant from the Edg Family

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

An essential role for ectodomain shedding in mammalian development

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Biology and genetics of hair

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

A novel phosphatidic acid-selective phospholipase A1 that produces lysophosphatidic acid

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Primers for exon-specific amplification of the KRT5 gene: identification of novel and recurrent mutations in epidermolysis bullosa simplex patients

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Identification and characterization of a novel lysophosphatidic acid receptor, p2y5/LPA6

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion

1 reference

https://api.crossref.org/works/10.1038%2FJID.2012.154

7 January 2021