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1

Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome

Wei Lu, Carrie L. Phillips, Paul D. Killen, Tommy Hlaing, Wilbur R. Harrison, F.F.B. Elder, Jeffrey H. Miner, Paul A. Overbeek, Miriam H. Meisler

Journal:

Year:

1999

Language:

english

File:

PDF, 675 KB

english, 1999

2

Mouse Brca1 : localization, sequence analysis and identification of evolutionarily conserved domains

Abel, Kenneth J., Xu, Junzhe, Yin, Gui-Ying, Lyons, Robert H., Meisler, Miriam H., Weber, Barbara L.

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 4.33 MB

english, 1995

3

Identification of Epilepsy Genes in Human and Mouse 1

Meisler, Miriam H., Kearney, Jennifer, Ottman, Ruth, Escayg, Andrew

Journal:

Annual Review of Genetics

Year:

2001

Language:

english

File:

PDF, 327 KB

english, 2001

4

Genetic interaction between Wnt7a and Lrp6 during patterning of dorsal and posterior structures of the mouse limb

Maja Adamska, Allison C. Billi, Susannah Cheek, Miriam H. Meisler

Journal:

Developmental Dynamics

Year:

2005

Language:

english

File:

PDF, 1.11 MB

english, 2005

5

Genetic interaction between Wnt7a and Lrp6 during patterning of dorsal and posterior structures of the mouse limb

Maja Adamska, Allison C. Billi, Susannah Cheek, Miriam H. Meisler

Journal:

Developmental Dynamics

Year:

2005

Language:

english

File:

PDF, 40 KB

english, 2005

6

Floxed allele for conditional inactivation of the voltage-gated sodium channel Scn8a (Nav1.6)

Stephen I. Levin, Miriam H. Meisler

Journal:

Year:

2004

Language:

english

File:

PDF, 229 KB

english, 2004

7

A hot spot for hotfoot mutations in the gene encoding the δ2 glutamate receptor

Ying Wang, Shinji Matsuda, Valerie Drews, Takashi Torashima, Miriam H. Meisler, Michisuke Yuzaki

Journal:

European Journal of Neuroscience

Year:

2003

Language:

english

File:

PDF, 481 KB

english, 2003

8

Conserved linkage of neurotrophin-3 and von Willebrand factor on mouse Chromosome 6

Lon L. Barrow, Karl Simin, Karen Mohlke, William C. Nichols, David Ginsburg, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 376 KB

english, 1993

9

Mouse chromosome 3

Michael F. Seldin, Jan-Bas Prins, Nanda R. Rodrigues, John A. Todd, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 799 KB

english, 1993

10

Insertional mutation of the hairless locus on mouse Chromosome 14

Julie M. Jones, James T. Elder, Karl Simin, Scott A. Keller, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 1.21 MB

english, 1993

11

Mapping of the neural retina leucine zipper gene,Nrl, to mouse Chromosome 14

Irina N. Bespalova, Qais Farjo, Douglas P. Mortlock, Anne U. Jackson, Miriam H. Meisler, Anand Swaroop, Margit Burmeister

Journal:

Mammalian Genome

Year:

1993

Language:

english

File:

PDF, 410 KB

english, 1993

12

Linkage of the structural gene for uroporphyrinogen I synthase to markers on mouse chromosome 9 in a cross between feral and inbred mice

Tammy K. Antonucci, Verne C. Chapman, Miriam H. Meisler

Journal:

Biochemical Genetics

Year:

1982

Language:

english

File:

PDF, 399 KB

english, 1982

13

Effects of theBgslocus on mouse β-galactosidase

Miriam H. Meisler

Journal:

Biochemical Genetics

Year:

1976

Language:

english

File:

PDF, 641 KB

english, 1976

14

Evidence that the same structural gene encodes testicular and adrenal 3β-hydroxysteroid dehydrogenase-isomerase

John R. D. Stalvey, Miriam H. Meisler, Anita H. Payne

Journal:

Biochemical Genetics

Year:

1987

Language:

english

File:

PDF, 494 KB

english, 1987

15

Cadmium metabolism incdm/cdmmice

Miriam Meisler, Craig Orlowski, Ellen Gross, John H. Bloor

Journal:

Biochemical Genetics

Year:

1979

Language:

english

File:

PDF, 260 KB

english, 1979

16

Three ENU-induced neurological mutations in the pore loopof sodium channelScn8a(Nav1.6) and a genetically linkedretinal mutation,rd13

David A. Buchner, Kevin L. Seburn, Wayne N. Frankel, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

2004

Language:

english

File:

PDF, 246 KB

english, 2004

17

Identification of evolutionarily conserved, functional noncoding elements in the promoter region of the sodium channel geneSCN8A

Valerie L. Drews, Kehui Shi, Georgius de Haan, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

2007

Language:

english

File:

PDF, 398 KB

english, 2007

18

DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes

Weizhen Ji, Feng Chen, Trang Do, Anh Do, Bruce A. Roe, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

2001

Language:

english

File:

PDF, 998 KB

english, 2001

19

Mutation watch

Journal:

Mammalian Genome

Year:

1997

Language:

english

File:

PDF, 891 KB

english, 1997

20

Meeting report: 10th international mouse genome conference

Sally A. Camper, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1997

Language:

english

File:

PDF, 1.02 MB

english, 1997

21

Mutation watch: PEX PLUS? gene(s) for X-linked hypophosphatemia and deafness

Journal:

Mammalian Genome

Year:

1997

Language:

english

File:

PDF, 151 KB

english, 1997

22

Mutation watch: Mouse brachyury (T), the T-box gene family, and human disease

Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1997

Language:

english

File:

PDF, 920 KB

english, 1997

23

Identification of genes within theKrddeletion on mouse Chromosome 19

Weizhen Ji, Bruce Herron, Julie M. Jones, Nancy A. Jenkins, Debra J. Gilbert, Neal G. Copeland, Richard Swank, Lorraine Flaherty, Miriam H. Meisler

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 57 KB

english, 1999

24

Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions

Miriam H. Meisler, Nicholas W. Plummer, Daniel L. Burgess, David A. Buchner, Leslie K. Sprunger

Journal:

Year:

2004

Language:

english

File:

PDF, 162 KB

english, 2004

25

Gene interactions and modifiers in epilepsy

Miriam H. Meisler

Journal:

Year:

2010

Language:

english

File:

PDF, 31 KB

english, 2010

26

DNA polymorphisms

MEISLER, MIRIAM H.

Journal:

Year:

1983

File:

PDF, 146 KB

1983

27

10.1038/74159

Meisler, Miriam H., Escayg, Andrew, MacDonald, Bryan T., Baulac, Stéphanie, Huberfeld, Gilles, An-Gourfinkel, Isabelle, Brice, Alexis, LeGuern, Eric, Moulard, Bruno, Chaigne, Denys, Buresi, Catherine,

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 304 KB

english, 2000

28

Induction of the Wnt antagonist, Dickkopf-1, contributes to the development of neuronal death in models of brain focal ischemia

Mastroiacovo, Federica, Busceti, Carla L, Biagioni, Francesca, Moyanova, Slavianka G, Meisler, Miriam H, Battaglia, Giuseppe, Caricasole, Andrea, Bruno, Valeria, Nicoletti, Ferdinando

Journal:

Journal of Cerebral Blood Flow and Metabolism

Year:

2008

Language:

english

File:

PDF, 802 KB

english, 2008

29

Mutation of a new sodium channel gene, Scn8a, in the mouse mutant ‘motor endplate disease’

Burgess, Daniel L., Kohrman, David C., Galt, James, Plummer, Nicholas W., Jones, Julie M., Spear, Brett, Meisler, Miriam H.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 498 KB

1995

30

Persistent Nav1.6 current at axon initial segments tunes spike timing of cerebellar granule cells

Nancy Osorio, Laurence Cathala, Miriam H. Meisler, Marcel Crest, Jacopo Magistretti, Patrick Delmas

Journal:

The Journal of Physiology

Year:

2010

Language:

english

File:

PDF, 1.34 MB

english, 2010

31

GM1-gangliosidosis: Chromosome 3 assignment of theβ-galactosidase-A gene (βGALA)

Thomas B. Shows, Linda R. Scrafford-Wolff, Judith A. Brown, Miriam H. Meisler

Journal:

Somatic Cell and Molecular Genetics

Year:

1979

Language:

english

File:

PDF, 1.07 MB

english, 1979

32

Insertional mutation of ‘classical’ and novel genes in transgenic mice

Miriam H. Meisler

Journal:

Trends in Genetics

Year:

1992

Language:

english

File:

PDF, 520 KB

english, 1992

33

De Novo Pathogenic SCN8A Mutation Identified by Whole-Genome Sequencing of a Family Quartet Affected by Infantile Epileptic Encephalopathy and SUDEP

Krishna R. Veeramah, Janelle E. O'Brien, Miriam H. Meisler, Xiaoyang Cheng, Sulayman D. Dib-Hajj, Stephen G. Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E. Eichler, Linda L. Restifo, Robert P. Eri

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 458 KB

english, 2012

34

Reduced spontaneous activity in the dorsal cochlear nucleus of Scn8a mutant mice

Kejian Chen, Leslie K. Sprunger, Miriam H. Meisler, Hardress J. Waller, Donald A. Godfrey

Journal:

Year:

1999

Language:

english

File:

PDF, 191 KB

english, 1999

35

Mouse p150Glued(Dynactin 1) cDNA Sequence and Evaluation as a Candidate for the Neuromuscular Disease Mutationmnd2

Wonhee Jang, John S. Weber, Mariko K. Tokito, Erika L.F. Holzbaur, Miriam H. Meisler

Journal:

Biochemical and Biophysical Research Communications

Year:

1997

Language:

english

File:

PDF, 122 KB

english, 1997

36

Progressive Loss of Striatal Neurons Causes Motor Dysfunction in MND2 Mutant Mice and Is Not Prevented by Bcl-2

Silvia Rathke-Hartlieb, Uwe Schlomann, Peter Heimann, Miriam H. Meisler, Harald Jockusch, Jörg W. Bartsch

Journal:

Experimental Neurology

Year:

2002

Language:

english

File:

PDF, 909 KB

english, 2002

37

Human PCK1 Encoding Phosphoenolpyruvate Carboxykinase Is Located on Chromosome 20q13.2

Hua Yu, Rachel Thun, Settara Chandrasekharappa, J.M. Trent, Ji Zhang, Miriam H. Meisler

Journal:

Year:

1993

File:

PDF, 166 KB

1993

38

The Genes Encoding Gonadal and Nongonadal Forms of 3β-Hydroxysteroid Dehydrogenase/Δ5-Δ4 Isomerase Are Closely Linked on Mouse Chromosome 3

Paul A. Bain, Miriam H. Meisler, Benjamin A. Taylor, Anita H. Payne

Journal:

Year:

1993

File:

PDF, 393 KB

1993

39

mnd2: A New Mouse Model of Inherited Motor Neuron Disease

Julie M. Jones, Roger L. Albin, Eva L. Feldman, Karl Simin, Timothy G. Schuster, Wesley A. Dunnick, John T. Collins, C.E. Chrisp, Benjamin A. Taylor, Miriam H. Meisler

Journal:

Year:

1993

File:

PDF, 928 KB

1993

40

Phosphoenolpyruvate Carboxykinase (GTP): Characterization of the Human PCK1 Gene and Localization Distal to MODY on Chromosome 20

Chao-Nan Ting, Daniel L. Burgess, Jeffrey S. Chamberlain, Tim P. Keith, Kathleen Falls, Miriam H. Meisler

Journal:

Year:

1993

File:

PDF, 566 KB

1993

41

Conserved Linkage of Early Growth Response 4, Annexin 4, and Transforming Growth Factor α on Mouse Chromosome 6

Lon L. Barrow, Karl Simin, Julie M. Jones, David C. Lee, Miriam H. Meisler

Journal:

Year:

1994

File:

PDF, 153 KB

1994

42

Kidney and Retinal Defects (Krd), a Transgene-Induced Mutation with a Deletion of Mouse Chromosome 19 That Includes the Pax2 Locus

Scot A. Keller, Julie M. Jones, Ann Boyle, Lon L. Barrow, Paul D. Killen, Daniel G. Green, Natalia V. Kapousta, Peter F. Hitchcock, Richard T. Swank, Miriam H. Meisler

Journal:

Year:

1994

File:

PDF, 1.26 MB

1994

43

Genetic and Physical Mapping at the Limb-Girdle Muscular Dystrophy Locus (LGMD2B) on Chromosome 2p

Rumaisa Bashir, Sharon Keers, Tom Strachan, Rita Passos-Bueno, Mayana Zatz, Jean Weissenbach, Denis Le Paslier, Miriam Meisler, Kate Bushby

Journal:

Year:

1996

Language:

english

File:

PDF, 272 KB

english, 1996

44

Localization of the Homolog of a Mouse Craniofacial Mutant to Human Chromosome 18q11 and Evaluation of Linkage to Human CLP and CPO

Andrew J. Griffith, Daniel L. Burgess, David C. Kohrman, Jennifer Yu, Jillian Blaschak, Susan H. Blanton, Michael Boehnke, Jacqueline T. Hecht, Joan Overhauser, Miriam H. Meisler

Journal:

Year:

1996

Language:

english

File:

PDF, 118 KB

english, 1996

45

Aup1, a Novel Gene on Mouse Chromosome 6 and Human Chromosome 2p13

Wonhee Jang, John S. Weber, Rumaisa Bashir, Kate Bushby, Miriam H. Meisler

Journal:

Year:

1996

Language:

english

File:

PDF, 113 KB

english, 1996

46

Localization of the Rhotekin GeneRTKNon the Physical Maps of Mouse Chromosome 6 and Human Chromosome 2p13 and Exclusion as a Candidate formnd2andLGMD2B

Wonhee Jang, John S. Weber, Emily B. Harkins, Miriam H. Meisler

Journal:

Year:

1997

Language:

english

File:

PDF, 90 KB

english, 1997

47

Calcium Channel β4 (CACNB4): Human Ortholog of the Mouse Epilepsy Genelethargic

Andrew Escayg, Julie M. Jones, Jennifer A. Kearney, Peter F. Hitchcock, Miriam H. Meisler

Journal:

Year:

1998

Language:

english

File:

PDF, 287 KB

english, 1998

48

Exon Organization, Coding Sequence, Physical Mapping, and Polymorphic Intragenic Markers for the Human Neuronal Sodium Channel GeneSCN8A

Nicholas W. Plummer, James Galt, Julie M. Jones, Daniel L. Burgess, Leslie K. Sprunger, David C. Kohrman, Miriam H. Meisler

Journal:

Year:

1998

Language:

english

File:

PDF, 662 KB

english, 1998

49

High-Resolution Genetic, Physical, and Transcript Map of themnd2Region of Mouse Chromosome 6

John S. Weber, Wonhee Jang, Karl Simin, Wei Lu, Jennifer Yu, Miriam H. Meisler

Journal:

Year:

1998

Language:

english

File:

PDF, 323 KB

english, 1998

50

Evolution and Diversity of Mammalian Sodium Channel Genes

Nicholas W. Plummer, Miriam H. Meisler

Journal:

Year:

1999

Language:

english

File:

PDF, 100 KB

english, 1999