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By John Tunison

[email protected]

Erik Hatzinger

GRANDVILLE -- To his mother, Erik Hatzinger is a single father who helps care for his elderly grandparents and does his best to provide for his 11-year-old son.

But police say Hatzinger's darker side is that of a serial burglar who may be responsible for breaking into more than 50 businesses in the Grand Rapids area.

"I find this very hard to believe," said Hatzinger's mother, Marjorie Hatzinger, who sees her son every day.

Police allege a 32-year-old burglary suspect caught early Thursday used the booty to support a crack cocaine habit and already has confessed to about 35 break-ins . The man was arrested after he tripped an alarm at Belle Tire, 2950 28th St. SW in Grandville, sometime after midnight.

Kent County sheriff's deputies did not name Hatzinger, pending an arraignment expected today, but another police source confirmed he is the suspect.

State police records show Grandville Police have sought a warrant against Hatzinger for felony burglary.

Sheriff's investigators think the suspect could be responsible for 50-70 burglaries since July in Grand Rapids, Grandville, Walker and the townships of Plainfield, Alpine and Grand Rapids.

"It was most every night he was out," sheriff's Lt. Kevin Kelley said. "The number of break-ins is pretty amazing for one guy working by himself."

Police said many of the burglaries were smash-and-grab incidents, with the suspect going for money in cash registers and small electronics he could later unload for cash. The suspect broke windows to gain entry.

"There was no real rhyme or reason to the locations," Kelley said. "He was simply breaking in when he thought there was an opportunity to do so."

Police said the suspect broke into more than a dozen hair salons. In all, he may have gotten $10,000 or more.

"He would get between $300-$800 a crack, on average," Kelley said.

Court records show Hatzinger already is facing a breaking and entering charge for an alleged Sept. 9 incident at El Burrito, 1971 Beltline Ave. NE, where $171 was taken from a register. He apparently did not confess to other burglaries at that time.

His criminal history includes two other breaking and entering cases -- convictions in 2008 for a building break-in and 2005 involving a car.

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The conversion is more suitable for the space and has been well-received, according to the mayor, who said fights on the basketball court didn't influence the change.

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The Village of New Hyde Park has converted its basketball court at Michael J. Nuzzi Field, seen on July 10, 2018, to volleyball and pickleball courts. (Credit: Newsday / Khristopher J. Brooks)

By Khristopher J. Brooks [email protected]
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A basketball court in New Hyde Park that last year was the source of fights and confrontations — promptingvillage officials to require ID from users — has been converted to a volleyball and pickleball area.

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Size Chart

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Select the proper size chart using the options below:

S M L XL XXL
Chest 35" - 37" 37" - 41" 41" - 44" 44" - 48" 48" - 53"
Waist 29" - 32" 32" - 35" 35" - 38" 38" - 43" 43" - 47"
Hips 35" - 37" 37" - 41" 41" - 44" 44" - 47" 47" - 50"
XS S M L XL XXL
Numeric Size 0-2 4-6 8-10 12-14 16-18 20-22
Bust 29" - 32" 32" - 35" 35" - 38" 38" - 41" 41" - 44" 44" - 48"
Waist 23" - 26" 26" - 29" 29" - 31" 31" - 34" 34" - 38" 38" - 42"
Hips 33" - 35" 35" - 38" 38" - 41" 41" - 44" 44" - 47" 47" - 50"
1X 2X 3X
Bust 44-48" 48-52" 52-56"
Waist 38-42" 42-46" 46-50"
Hip 47-50" 50-54" 54-58"
Regular Inseam 31" 31" 31"
Long Inseam 33" 33" 33"
Short Inseam 29" 29" 29"
XS S M L XL 1XL 2XL 3XL
A/B Cup 30" 32" 34" 36" 38"
B/C Cup 30" 32" 34" 36" 38" 40" 40" 40"
C/D Cup 30" 32" 34" 36" 38" 40" 40" 42"
D/E Cup 30" 32" 34" 36" 38" 40" 42" 44"
XS S M L XL
Avg. Age 6-8 8-10 10-12 12-13 13-15
Height 48" - 50" 50" - 54" 54" - 58" 58" - 62" 62" - 67"
Chest 25" - 26" 26" - 27" 27" - 29" 29" - 32" 32" - 35"
Waist 23" - 24" 24" - 25" 25" - 27" 27" - 28" 28" - 29"
Hip 27" - 28" 28" - 29" 29" - 31" 31" - 33" 33" - 35"
XS S M L XL
Avg. Age 6-8 8-10 10-12 12-13 13-15
Height 47" - 51" 51" - 55" 55" - 59" 59" - 63" 63" - 67"
Chest 25" - 27" 27" - 29" 29" - 31" 31" - 33" 33" - 35"
Waist 23" - 24" 24" - 25" 25" - 27" 27" - 28" 28" - 29"
Hip 27" - 29" 29" - 31" 31" - 33" 33" - 35" 35" - 37"
4 5 6 6X/7
Chest 22" 23" 24" 24"
Height 38-41" 41-43" 43-45" 45-48"
Waist 21" 21" 22" 22"
2T 3T 4T
Chest 20" 21" 22"
Height 33-35" 35-38" 38-41"
Waist 20" 20" 21"

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Immunofluorescence Staining of Cell Surface TACE— M2 cells were seeded onto coverslips that had been placed in 24-well plates. After overnight culture, they were transfected with extracellular FLAG-tagged TACE. 24 h after transfection, culture plates were placed on ice, and culture medium was replaced with 200 μl of cold, serum-free DMEM supplemented with 2% bovine serum albumin plus the anti-FLAG antibody (final concentration: 5 μg/ml). After a 30-min incubation on ice, coverslips were washed three times with cold PBS, fixed for 10 min with 100% methanol precooled to 4 °C, and reacted to fluorescein isothiocyanate-conjugated goat anti-mouse IgG diluted in PBS (1:400) for 30 min. After three additional washes, coverslips were mounted to glass slides, and viewed with a Nikon Eclipse E1000 fluorescent microscope.

Erk MAP Kinase Assay— CHOT, M1, and M2 cells grown on 10-cm plates at 80% confluence were serum-starved overnight. To determine the activation of the Erk MAPK pathway in response to growth factors, FBS (one-fourth volume of the medium) was added to the plates. After a 20-min incubation at 37 °C, cells were washed with cold PBS containing 1 m m sodium orthovanadate, 1 m m NaF, and 5 m m EDTA and lysed with 1% Nonidet P-40 prepared in the above PBS/orthovanadate/NaF/EDTA mix. The Erk2 protein in the cell lysates was immunoprecipitated with a specific antibody from Santa Cruz Biotechnology. The kinase activity of the precipitated Erk2 was assayed by measuring its ability to phosphorylate myelin basic protein using an Erk activity assay kit from Upstate Biotechnology (Lake Placid, NY) and [γ- 33 P]ATP. 33 P-phosphorylated myelin basic protein was spotted to phosphocellulose filters, washed to remove unincorporated radioactive ATP, and quantified by scintillation counting.

Sequencing Analyses and Cloning of Hamster TACE cDNAs— Total RNA from CHOT, M1, and M2 cells was isolated with the TRI Reagent (Sigma). 5′- and 3′-rapid amplification of cDNA ends (RACE) was accomplished with a Smart RACE kit from Clontech (Palo Alto, CA). RACE products were sequenced by an ABI PRISM-3100 Genetic Analyzer; the Analyzer-generated-fluorescent wave forms were visually examined to ensure the accuracy of data interpretation. The coding sequences of wild-type and mutated hamster TACE cDNA were cloned into the mammalian expression vector pRK5 for expression of untagged or FLAG epitope-tagged proteins. The sequence integrity of inserts in all resulting vectors was verified by automated sequencing.

Additional Mammalian Expression Vectors— Murine TACE was originally cloned by Amour et al. ( 62 ) and we obtained a plasmid containing its cDNA from Dr. C. Blobel (Memorial Sloan-Kettering Cancer Center). The murine TACE open reading frame was transferred to pRK5 where subsequent site-directed mutagenesis was performed using polymerase chain reaction (PCR)-based methodology. The expression vector we used for human TACE has been described previously ( Browse Commando Cotton Boy Shorts Red Pre Order Eastbay Cheap Pictures Cheap Sale Visit New Buy Cheap Footlocker Pictures met7D609
), as has the human transmembrane TGF-α expression vector pRK5α ( 63 ). A previously described expression vector for transmembrane TNF-α ( Macram茅 flared dress Buy Sale Online 0LXSA7TpVl
) was modified to express the type 2 membrane protein with an extracellular FLAG epitope tag at the C terminus.

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