(Q24655884)

1

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Suzanne M. Leal

4

object named as

S M Leal

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author name string

M Wajid

2

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W Ahmad

Journal of Medical Genetics

5

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language of work or name

English

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publication date

March 2006

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published in

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volume

43

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issue

3

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page(s)

274-9

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cites work

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Characterization of a 300 kbp region of human DNA containing the type II hair keratin gene domain

7 April 2017

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Characterization of new members of the human type II keratin gene family and a general evaluation of the keratin gene domain on chromosome 12q13.13

7 April 2017

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Comprehensive analysis of keratin gene clusters in humans and rodents

7 April 2017

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

7 April 2017

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A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes

7 April 2017

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Allegro, a new computer program for multipoint linkage analysis

7 April 2017

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Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

7 April 2017

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Faster sequential genetic linkage computations

7 April 2017

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The keratins and their disorders

7 April 2017

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Towards a new classification of ectodermal dysplasias.

28 September 2017

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Phenotypes, genotypes and their contribution to understanding keratin function

28 September 2017

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The Molecular Genetics of Keratin Disorders

28 September 2017

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A role for the 1A and L1 rod domain segments in head domain organization and function of intermediate filaments: structural analysis of trichocyte keratin

28 September 2017

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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

28 September 2017

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28 September 2017

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A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.

28 September 2017

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Expression of hair keratins in the adult nail unit: an immunohistochemical analysis of the onychogenesis in the proximal nail fold, matrix and nail bed.

28 September 2017

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Cytosine methylation and the fate of CpG dinucleotides in vertebrate genomes.

30 May 2018

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Family with "pure" hair-nail ectodermal dysplasia

28 November 2018

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Three keratin gene mutations account for the majority of dominant simplex epidermolysis bullosa cases within the population of Ireland

28 November 2018

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Computer programs for multilocus haplotyping of general pedigrees.

28 November 2018

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Divide-and-conquer crystallographic approach towards an atomic structure of intermediate filaments

28 November 2018

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12 December 2020

A novel mutation in the L12 domain of keratin 5 in the Köbner variant of epidermolysis bullosa simplex

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12 December 2020

Hypotrichosis and nail dysplasia: a novel hidrotic ectodermal dysplasia

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12 December 2020

Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia

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12 December 2020

Hair-nail dysplasia - a new pure autosomal dominant ectodermal dysplasia

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12 December 2020