Altered Trafficking of Mutant Connexin32

Molecular Cloning: A Laboratory Manual

2001 • 133,517 citations

Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family

1985 • 2,145 citations

Brefeldin A: insights into the control of membrane traffic and organelle structure.

1992 • 1,848 citations

Connections with Connexins: the Molecular Basis of Direct Intercellular Signaling

1996 • 1,301 citations

CONNEXINS, CONNEXONS, AND INTERCELLULAR COMMUNICATION

1996 • 1,180 citations

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

1993 • 1,055 citations

Gap junctions: New tools, new answers, new questions

1991 • 981 citations

Molecular cloning of cDNA for rat liver gap junction protein.

1986 • 715 citations

Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER

1993 • 492 citations

Trembler mouse carries a point mutation in a myelin gene

1992 • 418 citations

Connexin32 is a myelin-related protein in the PNS and CNS

1995 • 411 citations

Cell type-dependent variations in the subcellular distribution of alpha-mannosidase I and II

1993 • 336 citations

Topology of the 32-kd liver gap junction protein determined by site-directed antibody localizations.

1988 • 327 citations

Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32

1997 • 312 citations

Connexin32-null mice develop demyelinating peripheral neuropathy

1998 • 296 citations

A cellular mechanism governing the severity of Pelizaeus–Merzbacher disease

1996 • 224 citations

Role of potentially charged transmembrane residues in targeting proteins for retention and degradation within the endoplasmic reticulum.

1991 • 215 citations

Topological distribution of two connexin32 antigenic sites in intact and split rodent hepatocyte gap junctions.

1988 • 199 citations

Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease

1994 • 191 citations

Biology and Genetics of Hereditary Motor and Sensory Neuropathies

1995 • 179 citations

Mutations in the connexin 32 gene in X-linked dominant Charcot- Marie - Tooth disease (CMTX1)

1994 • 175 citations

Intermediate nerve conduction velocities define X‐linked Charcot‐Marie‐Tooth neuropathy families

1993 • 174 citations

MG-160

1989 • 168 citations

Connexin 32 mutations from X-linked Charcot-Marie-Tooth disease patients: functional defects and dominant negative effects.

1996 • 165 citations

Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport

1994 • 159 citations

Connexin32 and X-linked Charcot–Marie–Tooth Disease

1997 • 135 citations

Membrane insertion of gap junction connexins: polytopic channel forming membrane proteins.

1994 • 119 citations

Hereditary motor and sensory neuropathy, X‐linked

1987 • 116 citations

Arrest of proteolipid transport through the Golgi apparatus in Jimpy brain

1987 • 101 citations

Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-tooth neuropathy

1996 • 96 citations

Synthesis and assembly of human β1 gap junctions in BHK cells by DNA transfection with the human β1 cDNA

1995 • 88 citations

X-Linked Developmental Defects of Myelination: From Mouse Mutants to Human Genetic Diseases

1996 • 83 citations

Molecular Genetics of Demyelination: New Wrinkles on an Old Membrane

1997 • 73 citations

Retention of a cis Golgi protein requires polar residues on one face of a predicted alpha-helix in the transmembrane domain.

1993 • 70 citations

A connexin‐32 mutation associated with Charcot‐Marie‐Tooth disease does not affect channel formation in oocytes

1994 • 69 citations

TNFα Inhibits Schwann Cell Proliferation, Connexin46 Expression, and Gap Junctional Communication

1996 • 67 citations

Brefeldin A and the endocytic pathway Possible implications for membrane traffic and sorting

1992 • 61 citations

Gating characteristics of a steeply voltage-dependent gap junction channel in rat Schwann cells.

1993 • 55 citations

The topogenic fate of the polytopic transmembrane proteins, synaptophysin and connexin, is determined by their membrane-spanning domains

1995 • 54 citations

Transforming growth factor-beta 1 and forskolin modulate gap junctional communication and cellular phenotype of cultured Schwann cells

1995 • 52 citations

Distribution of P0 protein and the myelin-associated glycoprotein in peripheral nerves from Trembler mice

1991 • 34 citations

Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial clinical manifestations in female carriers

1980 • 33 citations

Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.

1978 • 26 citations

The Role of the Gap Junction Protein Connexin32 in the Myelin Sheath

1997 • 19 citations

Induction of connexin43 and gap junctional communication in PC12 cells overexpressing the carboxy terminal region of amyloid precursor protein

1996 • 16 citations

Connexin32 and X-linked Charcot-Marie-Tooth disease.

1996 • 15 citations

Connexin32 and X-Linked-Charcot-Marie-Tooth Disease

1996 • 11 citations

Optimized PCR using Vent polymerase.

1994 • 7 citations