Zobrazeno 1 - 10
of 54
pro vyhledávání: '"M. S. Deol"'
Publikováno v:
Brain research. 258(1)
The autosomal recessive gene quivering in the mouse causes deafness. The cochlea in mutant animals is histologically normal, and the thresholds for compound action potentials at the round window are also normal. But the thresholds for potentials in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fbcaeb76215adc2edc2e24887f92adb
https://pubmed.ncbi.nlm.nih.gov/24010186
https://pubmed.ncbi.nlm.nih.gov/24010186
Autor:
M. S. Deol
Publikováno v:
Acta Oto-Laryngologica. 92:331-336
The gene Bronx waltzer in the mouse leads to the absence or malformation of the inner hair cells as well as to abnormalities of the rods of Corti and degeneration of the maculae and cristae. This degeneration is so severe and appears so early that th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f34b2c51c04cdbb76ec915096fe30aa7
https://doi.org/10.3109/00016488109133269
https://doi.org/10.3109/00016488109133269
Autor:
M. S. Deol
Publikováno v:
Acta Oto-Laryngologica. 81:429-435
The developmental basis of the association of congenital deafness with hypothyroidism observed in several human syndromes was earlier investigated by experiments on mice. The offspring of females with chemically induced hypothyroidism were found to h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03eb2e4335ff12935221f2ad4553d7c8
https://doi.org/10.3109/00016487609119981
https://doi.org/10.3109/00016487609119981
Publikováno v:
Development. 96:295-302
Cattanach’s insertion (Is(In7;X)lCt or XCt) includes the normal allele at the albino locus (c+), which is subject to inactivation of the X chromosome carrying it, so that XCtX; cc mice have albino and pigmented patches. The X-autosome translocation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14b580227bc75d77531e5838765fd99f
https://doi.org/10.1242/dev.96.1.295
https://doi.org/10.1242/dev.96.1.295
Autor:
Gillian M. Truslove, M. S. Deol
Publikováno v:
Development. 78:291-298
Pink-eyed unstable (pun), an autosomal gene in the mouse, causes variegation of the coat. In some melanocytes it functions as the normal allele p+, producing dark pigment, and in others as the mutant p, producing light pigment. As a study of another
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53da72f024c797d47a1678e408e9da12
https://doi.org/10.1242/dev.78.1.291
https://doi.org/10.1242/dev.78.1.291
Autor:
Margaret C. Green, M. S. Deol
Publikováno v:
Journal of Experimental Zoology. 170:301-309
The effects of the mutant gene shaker-1 (sh-1) in the mouse include degeneration of the neural epithelium in the inner ear, which in places is so constructed that degeneration of minute areas, even single cells, can be identified. In Cattanach's tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d467bd9bac070cfef024287b2a82e76
https://doi.org/10.1002/jez.1401700307
https://doi.org/10.1002/jez.1401700307
Autor:
M. S. Deol
Publikováno v:
Development. 23:773-784
The gene dominant spotting in the mouse affects coat colour. The heterozygotes for the viable allele (Wv) have one or two white spots and a general greying of the coat. The homozygotes are entirely white. There is evidence that the gene causes abnorm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::477a4d6cdaa2e47d9b49ea467da7c0c0
https://doi.org/10.1242/dev.23.3.773
https://doi.org/10.1242/dev.23.3.773
Publikováno v:
Genetical Research. 1:50-58
Sixty-six individual tests on an array of skeletal variants showed an essential absence of parent-offspring correlations in the inbred strains C57BL, A and CBA in the mouse. It is concluded that these strains, and inbred strains of mice in general, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f152323966614c3f85b9dfe020065fe9
https://doi.org/10.1017/s0016672300000069
https://doi.org/10.1017/s0016672300000069
Autor:
M. S. Deol
Publikováno v:
Development. 11:493-512
A reinvestigation of the effects of the gene sy on the inner ear showed that the first abnormalities appear several days earlier than had hitherto been believed, and that they concern the periotic labyrinth and not the otic labyrinth. An excessive am
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df642f6cf09063a00328071387b53823
https://doi.org/10.1242/dev.11.3.493
https://doi.org/10.1242/dev.11.3.493
Autor:
M. S. Deol
Publikováno v:
Proceedings of the Royal Society of London. Series B. Biological Sciences. 155:78-95
This paper is dedicated to Professor L. C. Dunn ( Columbia University, New York ) in recognition of his long and distinguished career . Mice heterozygous for the T s gene have shorter tails and smaller bodies than their normal litter-mates. A study o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f66b46579bae6a5a89ef163bf12bbce4
https://doi.org/10.1098/rspb.1961.0058
https://doi.org/10.1098/rspb.1961.0058