(Q57315048)

8

0 references

author name string

Fabian Runkel

1

0 references

Matthias Klaften

2

0 references

Kerstin Koch

3

0 references

Volker Böhnert

4

0 references

Heinrich Büssow

5

0 references

Helmut Fuchs

6

0 references

Thomas Franz

7

0 references

publication date

December 2006

0 references

number of pages

11

1 reference

https://scigraph.springernature.com/pub.10.1007/s00335-006-0084-9

inferred from page(s)

published in

Mammalian Genome

0 references

volume

17

0 references

issue

12

0 references

page(s)

1172-1182

0 references

exact match

0 references

cites work

Induction of gene mutations in mice: the multiple endpoint approach.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-006-0084-9

Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-006-0084-9

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.

21 January 2018

1 reference

12 December 2020

The two-chain coiled-coil molecule of native epidermal keratin intermediate filaments is a type I-type II heterodimer

1 reference

12 December 2020

Screening for dysmorphological abnormalities—a powerful tool to isolate new mouse mutants

1 reference

12 December 2020

Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans.

1 reference

12 December 2020

Exposing the human nude phenotype.

1 reference

12 December 2020

The coiled coil of in vitro assembled keratin filaments is a heterodimer of type I and II keratins: use of site-specific mutagenesis and recombinant protein expression

1 reference

12 December 2020

Phenotypes, genotypes and their contribution to understanding keratin function

1 reference

12 December 2020

Functional analysis of keratin components in the mouse hair follicle inner root sheath

1 reference

12 December 2020

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

1 reference

12 December 2020

A comprehensive guide for the accurate classification of murine hair follicles in distinct hair cycle stages

1 reference

12 December 2020

Mutations in gasdermin 3 cause aberrant differentiation of the hair follicle and sebaceous gland

1 reference

12 December 2020

Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).

1 reference

12 December 2020

A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis

1 reference

12 December 2020

A Small Deletion Hotspot in the Type II Keratin Gene mK6irs1/Krt2-6g on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (Ca) Mutation

1 reference

12 December 2020

Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families

1 reference

12 December 2020

Keratins and the skin

1 reference

12 December 2020

Keratins of the human hair follicle

1 reference

12 December 2020

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

1 reference

12 December 2020

The catalog of human hair keratins. I. Expression of the nine type I members in the hair follicle

1 reference

12 December 2020

A splice site mutation in the gene of the human type I hair keratin hHa1 results in the expression of a tailless keratin isoform

1 reference

12 December 2020

New consensus nomenclature for mammalian keratins

1 reference

12 December 2020

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

1 reference

12 December 2020

The biology of hair follicles

1 reference

12 December 2020

1 reference

12 December 2020

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

1 reference

12 December 2020

Keratins and skin disorders

1 reference

12 December 2020

Schwann cell myelin ensheathing C.N.S. axons in the nerve fibre layer of the cat retina

1 reference

12 December 2020

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

1 reference

12 December 2020

BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

1 reference

12 December 2020

Towards defining the pathogenesis of the hairless phenotype.

1 reference

12 December 2020

The dominant alopecia phenotypes Bareskin, Rex-denuded, and Reduced Coat 2 are caused by mutations in gasdermin 3

1 reference

12 December 2020

Genes for intermediate filament proteins and the draft sequence of the human genome: novel keratin genes and a surprisingly high number of pseudogenes related to keratin genes 8 and 18

1 reference

12 December 2020

A structural scaffolding of intermediate filaments in health and disease

1 reference

12 December 2020

Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.

1 reference

12 December 2020

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

1 reference

12 December 2020

Human keratin diseases: hereditary fragility of specific epithelial tissues

1 reference

12 December 2020

The catalog of human hair keratins. II. Expression of the six type II members in the hair follicle and the combined catalog of human type I and II keratins

1 reference

12 December 2020

Cytokeratins as markers of follicular differentiation: an immunohistochemical study of trichoblastoma and basal cell carcinoma

1 reference

12 December 2020