ACNP - Italian Periodicals Catalogue

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Results: 1-11 |

Results: 11

CONNEXIN32-NULL MICE DEVELOP DEMYELINATING PERIPHERAL NEUROPATHY

Authors: SCHERER SS XU YT NELLES E FISCHBECK K WILLECKE K BONE LJ

Citation: Ss. Scherer et al., CONNEXIN32-NULL MICE DEVELOP DEMYELINATING PERIPHERAL NEUROPATHY, Glia, 24(1), 1998, pp. 8-20

MYELIN GENE-MUTATIONS UNDERLYING INHERITED HUMAN MYELINOPATHIES

Authors: SCHERER SS ABEL A FISCHBECK K BALICEGORDON RJ BONE LJ

Citation: Ss. Scherer et al., MYELIN GENE-MUTATIONS UNDERLYING INHERITED HUMAN MYELINOPATHIES, Journal of neurochemistry, 70, 1998, pp. 79-79

FUNCTIONAL GAP-JUNCTIONS IN THE SCHWANN-CELL MYELIN SHEATH

Authors: BALICEGORDON RJ BONE LJ SCHERER SS

Citation: Rj. Balicegordon et al., FUNCTIONAL GAP-JUNCTIONS IN THE SCHWANN-CELL MYELIN SHEATH, The Journal of cell biology, 142(4), 1998, pp. 1095-1104

CONNEXIN32 AND X-LINKED CHARCOT-MARIE-TOOTH-DISEASE

Authors: BONE LJ DESCHENES SM BALICEGORDON RJ FISCHBECK KH SCHERER SS

Citation: Lj. Bone et al., CONNEXIN32 AND X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, Neurobiology of disease, 4(3-4), 1997, pp. 221-230

OBSERVATIONS IN CONNEXIN32 TRANSGENIC MICE ARE CONSISTENT WITH A LOSSOF FUNCTION MECHANISM IN CMTX

Authors: ABEL A BONE LJ SCHERER SS FISCHBECK KH

Citation: A. Abel et al., OBSERVATIONS IN CONNEXIN32 TRANSGENIC MICE ARE CONSISTENT WITH A LOSSOF FUNCTION MECHANISM IN CMTX, American journal of human genetics, 61(4), 1997, pp. 1899-1899

CONNEXIN32 AND X-LINKED CHARCOT-MARIE-TOOTH-DISEASE

Authors: FISCHBECK KH DESCHENES SM BONE LJ SCHERER SS

Citation: Kh. Fischbeck et al., CONNEXIN32 AND X-LINKED CHARCOT-MARIE-TOOTH-DISEASE, Cold Spring Harbor Symposia on Quantitative Biology, 61, 1996, pp. 673-677

NEW CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTHDISEASE

Authors: BONE LJ DAHL N LENSCH MW CHANCE PF KELLY T LEGUERN E MAGI S PARRY G SHAPIRO H WANG S FISCHBECK KH

Citation: Lj. Bone et al., NEW CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTHDISEASE, Neurology, 45(10), 1995, pp. 1863-1866

PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION IN 21Q22.3,EXCLUSION OF SIM2 AS A CANDIDATE GENE FOR HOLOPROSENCEPHALY, AND MAPPING OF SIM2 TO A REGION OF CHROMOSOME-21 IMPORTANT FOR DOWN-SYNDROME

Authors: MUENKE M BONE LJ MITCHELL HF HART I WALTON K HALLJOHNSON K IPPEL EF DIETZBAND J KVALOY K FAN CM TESSIERLAVIGNE M PATTERSON D

Citation: M. Muenke et al., PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION IN 21Q22.3,EXCLUSION OF SIM2 AS A CANDIDATE GENE FOR HOLOPROSENCEPHALY, AND MAPPING OF SIM2 TO A REGION OF CHROMOSOME-21 IMPORTANT FOR DOWN-SYNDROME, American journal of human genetics, 57(5), 1995, pp. 1074-1079

THE DISEASE MECHANISM FOR X-LINKED CHARCOT-MARIE-TOOTH DISEASE

Authors: BONE LJ SCHERER SS BALICEGORDON RJ PAUL DL FISCHBECK KH

Citation: Lj. Bone et al., THE DISEASE MECHANISM FOR X-LINKED CHARCOT-MARIE-TOOTH DISEASE, American journal of human genetics, 57(4), 1995, pp. 1366-1366

A YAC CONTIG FOR XQ13

Authors: BONE LJ JOHANSON R CHEN KL NIEUWENHUIJSEN BW PUCK JM FISCHBECK KH

Citation: Lj. Bone et al., A YAC CONTIG FOR XQ13, Cytogenetics and cell genetics, 67(4), 1994, pp. 331-331

CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE

Authors: BERGOFFEN J SCHERER SS WANG S SCOTT MO BONE LJ PAUL DL CHEN K LENSCH MW CHANCE PF FISCHBECK KH

Citation: J. Bergoffen et al., CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE, Science, 262(5142), 1993, pp. 2039-2042

Risultati: 1-11 |