|
Title:
Leukotriene modifiers
Author(s):
Kelly HW
Source:
PEDIATRICS
v.
109(#1) pp. 170-171 JAN 2002
Abstract:
No
abstract
Title:
Behcet's disease: Endovascular management of a ruptured
peripheral arterial aneurysm
Author(s):
Kasirajan K, Marek JM, Langsfeld M
Source:
JOURNAL OF VASCULAR SURGERY
v.
34(#6) pp. 1127-1129 DEC 2001
Abstract:
Traditionally,
bypass grafts are at a high risk for thrombosis or anastomotic
degeneration in patients with Behcet's disease. We report the
successful deployment of a
vein-covered stent across the neck of a ruptured peripheral
arterial aneurysm, via a remote site access, with
intermediate-term follow-up. Covered
stents may represent an attractive alternative to open surgical
bypass
for the management of aneurysms in patients with Behcet's
disease
Title:
A polycystin-1, E-cadherin and beta-catenin complex is
disrupted in polycystic kidney
disease cells
Author(s):
Roitbak T, Bacallao R, Ward C, Harris P, Woo D,
Wandinger-Ness A
Source:
MOLECULAR BIOLOGY OF THE CELL
v.
12(SS) pp. 397A-398A NOV 2001
Abstract:
No
abstract
Title:
Genetic ablation of the t-SNARE SNAP-25 distinguishes
mechanisms of neuroexocytosis
Author(s):
Washbourne P, Thompson PM, Carta M, Costa ET, Mathews JR,
Lopez-Bendito G, Molnar Z, Becher MW, Valenzuela CF,
Partridge LD, Wilson MC
Source:
NATURE NEUROSCIENCE
v.
5(#1) pp. 19-26 JAN 2002
Abstract:
Axon
outgrowth during development and neurotransmitter release depends on
exocytotic mechanisms, although what protein machinery is
common to or differentiates
these processes remains unclear. Here we show that the neural
t-SNARE target-membrane-associated-soluble N-ethylmaleimide
fusion protein attachment
protein (SNAP) receptor) SNAP-25 is not required for nerve growth
or stimulus-independent neurotransmitter release, but is
essential for evoked synaptic
transmission at neuromuscular junctions and central synapses. These
results demonstrate that the development of neurotransmission
requires the recruitment of a
specialized SNARE core complex to meet the demands of
regulated exocytosis
Title:
Rab7 interacts with hVps34 and regulates late endosomal
trafficking
Author(s):
Stein MP, Feng Y, Wandinger-Ness A
Source:
MOLECULAR BIOLOGY OF THE CELL
v.
12(SS) pp. 249A-249A NOV 2001
Abstract:
No
abstract
Title:
Sexual function in women with and without urinary
incontinence
and/or pelvic organ prolapse
Author(s):
Rogers GR, Villarreal A, Kammerer-Doak D, Qualls C
Source:
INTERNATIONAL UROGYNECOLOGY JOURNAL AND PELVIC FLOOR
DYSFUNCTION
v.
12(#6) pp. 361-365 NOV 2001
Abstract:
The
sexual function of women with and without urinary incontinence
and/or pelvic organ prolapse
(UI/POP) was compared using a condition-specific
validated questionnaire, the Pelvic Organ Prolapse/Urinary
Incontinence Sexual Questionnaire
(PISQ). Eighty-three women with UI/POP and 56 without agreed to
participate. PISQ scores were significantly lower among women
with UI/POP than in those
without (P = 0.003). No differences in the stages of sexual
excitement were noted between groups. The frequency of
intercourse was less with
UI/POP than without (P = 0.04). Women with UI/POP restricted sexual
activity for fear of losing urine more frequently than did
those without (P = 0.005). No
differences were reported in patients' or partners' sexual
satisfaction. This study found that women with UI/POP have
poorer sexual functioning
than those without, as measured by the PISQ, and report less
frequent sexual activity. In addition, women with UI/POP are
more likely to restrict
sexual activity for fear of incontinence, although they report
similar levels of satisfaction with their sexual
relationships as do women
without UI/POP
Title:
Interaction with BRCA2 suggests a role for filamin-1 (hsFLNa)
in DNA damage response
Author(s):
Yuan Y, Shen ZY
Source:
JOURNAL OF BIOLOGICAL CHEMISTRY
v.
276(#51) pp. 48318-48324 DEC 21, 2001
Abstract:
The
BRCA2 tumor suppressor plays significant roles in DNA damage
response. The human actin
binding protein filamin-1 (hsFLNa, also known as ABP-280)
participates in orthogonal actin network, cellular stress
responses, signal transduction,
and cell migration. Through a yeast two-hybrid system, an in
vitro binding assay, and in vivo co-immunoprecipitations, we
identified an interaction
between BRCA2 and hsFLNa. The hsFLNa binding domain of BRCA2 was
mapped to an internal conserved region, and the
BRCA2-interacting domain of hsFLNa
was mapped to its C terminus. Although hsFLNa is known for its
cytoplasmic functions in cell migration and signal
transduction, some hsFLNa resides
in the nucleus, raising the possibility that it participates in DNA
damage response through a nuclear interaction with BRCA2.
Lack of hsFLNa renders a
human melanoma cell line (M2) more sensitive to several genotoxic
agents including gamma irradiation, bleomycin, and
ultraviolet-c light. These results
suggest that BRCA2/hsFLNa interaction may serve to connect
cytoskeletal signal transduction to DNA damage response
pathways
Title:
US for detecting renal calculi with nonenhanced CT as a
reference standard
Author(s):
Fowler KAB, Kocken JA, Duchesne JH, Williamson MR
Source:
RADIOLOGY
v.
222(#1) pp. 109-113 JAN 2002
Abstract:
PURPOSE:
To determine the sensitivity, and specificity of ultrasonography
(US) for detecting
parenchymal and renal pelvis calculi and to establish the
accuracy of US for determining the size and number of
calculi.
MATERIALS
AND METHODS: A total of 123 US and computed tomographic (CT)
examinations were compared retrospectively for the presence
of renal calculi. The
sensitivity of US was determined for individual calculi and at least
one calculus per examination.
Retrospective findings were compared with the
original US interpretation. The sizes of calculi in longest
axis were compared on US and
CT images' and the US detection of calculi in the left and right
kidneys was compared. The use of US for detecting the full
extent of calculus burden was
evaluated in patients with multiple calculi.
RESULTS:
US depicted 24 of 101 calculi identified at CT, yielding a
sensitivity of 24% and a specificity of 90%. There was no
substantial difference for
the detection of calculi in the right and left kidneys. The.
sensitivity of US for any calculi in a patient was 44%, equal
to that of the original
US-interpretation. US enabled identification of 39% of patients with
multiple calculi and demonstrated all calculi in 17% of these
patients. The mean size of
calculi detected with US was 7.1 mm 1.2 (95% CI); 73% of calculi
not visualized at US were less than 3.0 mm in size. Calculus
size based on US and CT
measurements was concordant in 79% of cases and differed by a mean
of 1.5 mm 0.7.
CONCLUSION:
US is of limited value for detecting renal calculi
Title:
Anti-gravity effects in the Sachs theory of electrodynamics
Author(s):
Anastasovski PK, Bearden TE, Ciubotariu C, Coffey WT,
Crowell LB, Evans GJ, Evans MW, Flower R, Labounsky A,
Lehnert B, Meszaros M, Molnar PR, Roy S, Vigier JP
Source:
FOUNDATIONS OF PHYSICS LETTERS
v.
14(#6) pp. 601-605 DEC 2001
Abstract:
It
is demonstrated to a first approximation that anti-gravity effects
can occur in the most general
theory of electromagnetism, developed by Sachs [1]
from the irreducible representations of the Einstein group
Title:
Dendritic cells: Immune regulators in health and disease
Author(s):
Lipscomb MF, Masten BJ
Source:
PHYSIOLOGICAL REVIEWS
v.
82(#1) pp. 97-130 JAN 2002
Abstract:
Dendritic
cells (DCs) are bone marrow-derived cells of both lymphoid and
myeloid stem cell origin that populate all lymphoid organs
including the thymus, spleen,
and lymph nodes, as well as nearly all nonlymphoid tissues and
organs. Although DCs are a moderately diverse set of cells,
they all have potent
antigen-presenting capacity for stimulating naive, memory, and
effector T cells. DCs are
members of the innate immune system in that they can respond
to dangers in the host environment by immediately generating
protective cytokines. Most
important, immature DCs respond to danger signals in the
microenvironment by maturing, i.e., differentiating, and
acquiring the capacity to
direct the development of primary immune responses appropriate to
the type of danger perceived. The powerful adjuvant activity
that DCs possess in
stimulating specific CD4 and CD8 T cell responses has made them
targets in vaccine
development strategies for the prevention and treatment of
infections, allograft
reactions, allergic and autoimmune diseases, and cancer. This review
addresses the origins and migration of DCs to their sites of
activity, their basic biology
as antigen-presenting cells, their roles in important human
diseases and, finally, selected strategies being pursued to
harness their
potent antigen-stimulating activity
Title:
Derivation of the B-(3) field and concomitant vacuum energy
density from the Sachs theory of electrodynamics
Author(s):
Anastasovski PK, Bearden TE, Ciubotariu C, Coffey WT,
Crowell LB, Evans GJ, Evans MW, Flower R, Labounsky A,
Lehnert B, Meszaros M, Molnar PR, Moscicki JK, Roy S, Vigier
JP
Source:
FOUNDATIONS OF PHYSICS LETTERS
v.
14(#6) pp. 589-593 DEC 2001
Abstract:
The
archetypical and phaseless vacuum magnetic flux density of O(3)
electrodynamics, the B-(3) field, is derived from the
irreducible representation of
the Einstein group and is shown to be accompanied by a
vacuum energy density which depends directly on the square.
of the scalar curvature R of
curved spacetime. The B-(3) field and the vacuum energy density
are obtained respectively from the non-Abelian part of the
field tensor F-mu nu and the
non-Abelian part of the metrical field equation. Both of these
terms are given by Sachs [5]
Title:
Development of the Sachs theory of electrodynamics
Author(s):
Anastasovski PK, Bearden TE, Ciubotariu C, Coffey WT,
Crowell LB, Evans J, Evans MW, Flower R, Labounsky A, Lehnert
B, Meszaros M, Molnar PR, Roy
S, Vigier JP
Source:
FOUNDATIONS OF PHYSICS LETTERS
v.
14(#6) pp. 595-600 DEC 2001
Abstract:
The
most general form of electro dynamics has been derived by Sachs [1]
from the irreducible
representations of the Einstein group. In this paper the Sachs
theory is developed as a gauge theory with a vacuum
four-current i(j)(mu). The B
Cyclic Theorem O(3) electrodynamics is derived from a consideration
of four-vectors appearing in
the Sachs theory, and electromagnetic helicity, expressed
in terms of the B-(3) field of O(3) electrodynamics, is derived from
the more general Sachs theory
Title:
Discriminators between hantavirus-infected and -uninfected
persons enrolled in a trial of intravenous ribavirin for
presumptive hantavirus pulmonary syndrome
Author(s):
Chapman LE, Ellis BA, Koster FT, Sotir M, Ksiazek TG, Mertz GJ,
Rollin PE, Baum KF, Pavia AT, Christenson JC, Rubin PJ,
Jolson HM, Behrman RE, Khan AS, Bell LJW, Simpson GL, Hawk J,
Holman RC, Peters CJ
Source:
CLINICAL INFECTIOUS DISEASES
v.
34(#3) pp. 293-304 FEB 1, 2002
Abstract:
To
provide a potentially therapeutic intervention and to collect
clinical and laboratory data
during an outbreak of hantavirus pulmonary syndrome (HPS), 140
patients from the United States with suspected HPS were
enrolled for investigational
intravenous ribavirin treatment. HPS was subsequently
laboratory confirmed in 30 persons and not confirmed in 105
persons with adequate
specimens. Patients with HPS were significantly more likely than
were hantavirus-negative
patients to report myalgias from onset of symptoms through
hospitalization, nausea at outpatient presentation, and
diarrhea and nausea at the
time of hospitalization; they were significantly less likely to
report respiratory symptoms
early in the illness. The groups did not differ with
regard to time from the onset of illness to the point at
which they sought care; time
from onset, hospitalization, or enrollment to death was
significantly shorter for patients with HPS. At the time of
hospitalization, patients
with HPS more commonly had myelocytes, metamyelocytes, or
promyelocytes on a peripheral blood smear, and significantly
more of them had thrombocytopenia,
hemoconcentration, and hypocapnia. Patterns of clinical
symptoms, the pace of clinical evolution, and specific
clinical laboratory
parameters discriminated between these 2 groups
Title:
Expression of the granzyme B inhibitor, protease
inhibitor 9, by tumor cells
in patients with non-Hodgkin and Hodgkinlymphoma: a novel protective
mechanism for tumor cells to
circumvent the immune system?
Author(s):
Bladergroen BA, Meijer CJLM, ten Berge RL, Hack CE, Muris JJF,
Dukers DF, Chott A, Kazama Y, Oudejans JJ, van Berkum O,
Kummer JA
Source:
BLOOD
v.
99(#1) pp. 232-237 JAN 1, 2002
Abstract:
In
tumor cells, the serine protease granzyme B is the primary mediator
of apoptosis induced by
cytotoxic T lymphocytes (CTLs)/natural killer (NK) cells.
The human intracellular serpin proteinase inhibitor 9 (PI9)
is the only known human
protein able to inhibit the proteolytic activity of granzyme B. When
present in the cytoplasm of T lymphocytes, PI9 is thought to
protect CTLs against
apoptosis induced by their own misdirected granzyme B. Based on the
speculation that tumors may also express PI9 to escape CTL/NK
cell surveillance,
immunohistochemical studies on the expression of PI9 in various
lymphomas were performed. Ninety-two cases of T-cell
non-Hodgkin lymphoma (NHL),
76 cases of B-cell NHL, and 57 cases of Hodgkin lymphomas were
stained with a PI9-specific
monoclonal antibody. In T-cell NHL, highest PI9 expression
was found in the extranodal T-cell NHL. In nearly 90% of
enteropathy-type T-cell NHLs
and 80% of NK/T-cell, nasal-type lymphomas, the majority of the
tumor cells expressed PI9. In nodal T-anaplastic large cell
lymphomas and peripheral
T-cell lymphomas (not otherwise specified), PI9 expression occurred
less frequently. In B-cell NHL, PI9 expression was associated
with high-grade malignancy;
43% of diffuse large B-cell lymphomas showed PI9(+) tumor cells.
Finally, PI9 expression was also found in 10% of Hodgkin
lymphomas. This is the first
report describing the expression of the granzyme B inhibitor PI9 in
human neoplastic cells in vivo. Expression of this inhibitor
is yet another mechanism used
by tumor cells to escape their elimination by cytotoxic
lymphocytes
Title:
Copolymer 1 reduces relapse rate and improves disability
in
relapsing-remitting multiple
sclerosis: Results of a phase III
multicenter, double-blind,
placebo-controlled trial
Author(s):
Johnson KP, Brooks BR, Cohen JA, Ford CC, Goldstein J, Lisak
RP,
Myers LW, Panitch HS, Rose JW,
Schiffer RB, Vollmer T,
Weiner LP, Wolinsky JS
Source:
NEUROLOGY
v.
57(#12/S5) pp. S16-S24 DEC 2001
Abstract:
We
studied copolymer 1 (Copaxone) in a multicenter (11-university)
phase III trial
of patients with relapsing-remitting multiple sclerosis (MS). Two
hundred fifty-one patients were
randomized to receive copolymer I (n = 125) or
placebo (n = 126) at a dosage of 20
mg by daily subcutaneous injection for 2
years. The primary end point was a
difference in the MS relapse rate. The
final 2-year relapse rate was 1.19
+/- 0.13 for patients receiving copolymer 1
and 1.68 +/- 0.13 for those
receiving placebo, a 29% reduction in favor of
copolymer 1 (p = 0.007) (annualized
rates = 0.59 for copolymer 1 and 0.84 for
placebo). Trends in the proportion
of relapse-free patients and median time to
first relapse favored copolymer 1.
Disability was measured by the Expanded
Disability Status Scale (EDSS),
using a two-neurologist (examining and
treating) protocol. When the
proportion of patients who improved, were
unchanged, or worsened by greater
than or equal to1 EDSS step from baseline to
conclusion (2 years) was evaluated,
significantly more patients receiving
copolymer 1 were found to have
improved and more receiving placebo worsened (p
= 0.037). Patient withdrawals were
19 (15.2%) from the copolymer 1 group and
17 (13.5%) from the placebo group
at approximately the same intervals. The
treatment was well tolerated. The
most common adverse experience was an
injection-site reaction. Rarely, a
transient self-limited systemic reaction
followed the injection in 15.2% of
those receiving copolymer 1 and 3.2% of
those receiving placebo, This
reaction was characterized by flushing or chest
tightness with palpitations,
anxiety, or dyspnea and commonly lasted for 30
seconds to 30 minutes. This
rigorous study confirmed the findings of a
previous pilot trial and
demonstrated that copolymer 1 treatment can
significantly and beneficially
alter the course of relapsing-remitting MS in a
well-tolerated fashion
|