Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. (Q44306011)

1 December 2017

title

Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. (English)

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1 December 2017

6

Roderick T Bronson

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1 December 2017

9

Muriel T Davisson

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1 December 2017

Kenneth R Johnson

1

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1 December 2017

Priscilla W Lane

2

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1 December 2017

Susan A Cook

3

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1 December 2017

Belinda S Harris

4

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1 December 2017

Patricia F Ward-Bailey

5

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1 December 2017

Bonnie L Lyons

7

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1 December 2017

Leonard D Shultz

8

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1 December 2017

publication date

1 January 2003

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1 December 2017

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1 December 2017

volume

81

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1 December 2017

issue

1

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1 December 2017

page(s)

6-14

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

1 December 2017

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Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene

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Uncv (uncovered): a new mutation causing hairloss on mouse chromosome 11

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

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

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A mutation in the epidermal growth factor receptor in waved-2 mice has a profound effect on receptor biochemistry that results in impaired lactation

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Molecular cloning of the mouse grb2 gene: differential interaction of the Grb2 adaptor protein with epidermal growth factor and nerve growth factor receptors

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Growth factor-induced tyrosine phosphorylation of Hrs, a novel 115-kilodalton protein with a structurally conserved putative zinc finger domain

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Mammalian Grb2 regulates multiple steps in embryonic development and malignant transformation.

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Hrs, a FYVE finger protein localized to early endosomes, is implicated in vesicular traffic and required for ventral folding morphogenesis

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Epiregulin, a novel member of the epidermal growth factor family, is an autocrine growth factor in normal human keratinocytes

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Cloning and biological activity of epigen, a novel member of the epidermal growth factor superfamily

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Transgenic expression of the human amphiregulin gene induces a psoriasis-like phenotype

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Prolonged survival of mouse skin allografts in recipients treated with donor splenocytes and antibody to CD40 ligand

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A new mouse mutation causing male sterility and histoincompatibility.

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Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins

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A Macintosh program for storage and analysis of experimental genetic mapping data

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7 January 2021

10.1016/S0888-7543(02)00013-7

Identifiers

DOI

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1 December 2017

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