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Admin24.07.2021

Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency — MD Anderson Cancer Center

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Skin lesions were characterized by sparse rough coat, bare patches around the eyes and neck, and a scratching behavior throughout life.
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Admin18.07.2021

Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency — MD Anderson Cancer Center

Linkage analysis using a set of molecular markers and an F2 intersubspecific cross indicated that the mutation maps to the central region of mouse chromosome 13, in a region homologous to human chromosome 5q22-q35.
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Admin06.07.2021

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AB - A spontaneous recessive mutation named nackt symbol: nkt affecting hair growth and T-cell development was discovered in a moderately inbred stock of mice.
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Admin10.07.2021

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PY - 1999 Y1 - 1999 N2 - A spontaneous recessive mutation named nackt symbol: nkt affecting hair growth and T-cell development was discovered in a moderately inbred stock of mice.
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Admin03.09.2021

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Linkage analysis using a set of molecular markers and an F 2 intersubspecific cross indicated that the mutation maps to the central region of mouse chromosome 13, in a region homologous to human chromosome 5q22-q35.
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Linkage analysis using a set of molecular markers and an F2 intersubspecific cross indicated that the mutation maps to the central region of mouse chromosome 13, in a region homologous to human chromosome 5q22-q35.
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Admin10.06.2021

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That may not sound promising, but it is.
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Admin29.06.2021

Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency — MD Anderson Cancer Center

Skin lesions were characterized by sparse rough coat, bare patches around the eyes and neck, and a scratching behavior throughout life.
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Admin05.09.2021

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Admin17.06.2021

Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency — MD Anderson Cancer Center

Linkage analysis using a set of molecular markers and an F2 intersubspecific cross indicated that the mutation maps to the central region of mouse chromosome 13, in a region homologous to human chromosome 5q22-q35.
1001