Findings of Research Misconduct, 2707-2708 [2015-00802]
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Federal Register / Vol. 80, No. 12 / Tuesday, January 20, 2015 / Notices
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2707
Program Act of 2000. The initial
proposed definition for the class being
evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Lawrence Livermore National
Laboratory.
Location: Livermore, California.
Job Titles and/or Job Duties: All employees
of the Department of Energy, its predecessor
agencies, and its contractors and
subcontractors who worked in any area.
Period of Employment: January 1, 1974
through December 31, 1995.
FOR FURTHER INFORMATION CONTACT:
Stuart L. Hinnefeld, Director, Division
of Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 1090 Tusculum
Avenue, MS C–46, Cincinnati, OH
45226–1938, Telephone 877–222–7570.
Information requests can also be
submitted by email to DCAS@CDC.GOV.
John Howard,
Director, National Institute for Occupational
Safety and Health.
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Findings of Research Misconduct
FEDERAL ELECTION COMMISSION
DATE: January 15, 2015.
James Petrick,
General Counsel, Federal Retirement Thrift
Investment Board.
[FR Doc. 2015–00921 Filed 1–15–15; 4:15 pm]
SUMMARY:
[FR Doc. 2015–00680 Filed 1–16–15; 8:45 am]
Sunshine Act Meeting
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Federal Register Citation of Previous
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This meeting will be continued on
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Decision to Evaluate a Petition To
Designate a Class of Employees From
the Lawrence Livermore National
Laboratory in Livermore, California, To
Be Included in the Special Exposure
Cohort
National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention, Department of Health
and Human Services.
ACTION: Notice.
AGENCY:
NIOSH gives notice as
required by 42 CFR 83.12(e) of a
decision to evaluate a petition to
designate a class of employees from the
Lawrence Livermore National
Laboratory in Livermore, California, to
be included in the Special Exposure
Cohort under the Energy Employees
Occupational Illness Compensation
SUMMARY:
PERSON TO CONTACT FOR INFORMATION:
Shelley E. Garr,
Deputy Secretary of the Commission.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
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Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Notice is hereby given that
the Office of Research Integrity (ORI)
has taken final action in the following
case:
Bin Kang, Ph.D., Oklahoma Medical
Research Foundation: Based on the
Respondent’s admission, an assessment
conducted by the Oklahoma Medical
Research Foundation (OMRF), and
additional analysis conducted by ORI in
its oversight review, ORI found that Dr.
Bin Kang, Postdoctoral Fellow,
Immunobiology and Cancer Research
Program, OMRF, engaged in research
misconduct in research supported by
National Institute of Allergy and
Infectious Diseases (NIAID), National
Institutes of Health (NIH), grants
AI056129 and AI104057.
ORI and OMRF found that
Respondent engaged in research
misconduct by reporting falsified data
in:
• ‘‘Asb2 regulates the activity of SCF
E3 ubiquitin ligases by antagonizing
CAND1-mediated exchange of F-box
proteins,’’ submitted to Molecular Cell
on June 26, 2014; hereafter referred to as
the ‘‘original Molecular Cell
manuscript’’
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2708
Federal Register / Vol. 80, No. 12 / Tuesday, January 20, 2015 / Notices
• the revised version of ‘‘Asb2
regulates the activity of SCF E3
ubiquitin ligases by antagonizing
CAND1-mediated exchange of F-box
proteins,’’ submitted to Molecular Cell
on September 29, 2014; hereafter
referred to as the ‘‘revised Molecular
Cell manuscript
• grant application CA189216–01
submitted to the National Cancer
Institute (NCI), NIH; hereafter referred to
as the ‘‘original NCI grant application’’
• grant application CA189216–01A1
submitted to NCI, NIH; hereafter
referred to as the ‘‘revised NCI grant
application’’
ORI found that Respondent
knowingly falsified and/or fabricated
Western blot gel images by duplication,
reuse and relabeling, and/or alteration
through contrast, rotation, and/or scale
of the images.
Specifically, Respondent included
falsified images in all of the figures
(Figures 1–6 and S1–5) in the original
Molecular Cell manuscript, all of the
figures (Figures 1–6 and S1–7) in the
revised
Molecular Cell manuscript, Figures 2–
4, 9, and 11 in the original NCI grant
application, and Figures 3–5, 10, and 11
in the revised NCI grant application.
Dr. Kang has entered into a Voluntary
Settlement Agreement (Agreement) and
has voluntarily agreed for a period of
three (3) years, beginning on December
23, 2014:
(1) To have his research supervised;
Respondent agreed to ensure that prior
to the submission of an application for
U.S. Public Health Service (PHS)
support for a research project on which
the Respondent’s participation is
proposed and prior to Respondent’s
participation in any capacity on PHSsupported research, the institution
employing him must submit a plan for
supervision of his duties to ORI for
approval; the plan for supervision must
be designed to ensure the scientific
integrity of Respondent’s research
contribution; Respondent agreed that he
will not participate in any PHSsupported research until such a
supervision plan is submitted to and
approved by ORI; Respondent agreed to
maintain responsibility for compliance
with the agreed upon plan for
supervision;
(2) that any institution employing him
must submit, in conjunction with each
application for PHS funds, or report,
manuscript, or abstract involving PHSsupported research in which
Respondent is involved, a certification
to ORI that the data provided by
Respondent are based on actual
experiments or are otherwise
legitimately derived and that the data,
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14:47 Jan 16, 2015
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procedures, and methodology are
accurately reported in the application,
report, manuscript, or abstract; and
(3) to exclude himself voluntarily
from serving in any advisory capacity to
PHS including, but not limited to,
service on any PHS advisory committee,
board, and/or peer review committee, or
as a consultant.
Dated: January 13, 2015.
E.J. Holland, Jr.,
Assistant Secretary for Administration (ASA).
FOR FURTHER INFORMATION CONTACT:
Centers for Medicare & Medicaid
Services
Acting Director, Office of Research
Integrity, 1101 Wootton Parkway, Suite
750, Rockville, MD 20852, (240) 453–
8200.
Donald Wright,
Acting Director, Office of Research Integrity.
[FR Doc. 2015–00802 Filed 1–16–15; 8:45 am]
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DEPARTMENT OF HEALTH AND
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Continued Approval of the
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ACTION: Final notice.
AGENCY:
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Office of the Secretary; Office of
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Statement of Organization, Functions,
and Delegations of Authority
Part A, Office of the Secretary,
Statement of Organization, Functions,
and Delegations of Authority for the
Department of Health and Human
Services, is being amended at Chapter
AK, Office of Medicare Hearings and
Appeals (OMHA), as last amended at 70
FR 36386–36387, dated June 23, 2005,
and most recently at 76 FR 19995 (Apr.
11, 2011) as follows:
I. Under Section AK.10, Organization,
delete the bullets and sub-bullets
after the phrase, ‘‘OMHA consists of
the following components,’’ and
replace with the following:
• Medicare Hearings and Appeals
Chief Judge’s Office (CJO) (Headquarters
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— Office of Operations
— Office of Programs
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Paragraph B, replace ‘‘Medicare
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III. Under Section AK.20, Functions,
Paragraph B, ‘‘Medicare Hearings
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with ‘‘Associate Chief
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(ACALJ).’’
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This final notice announces
our decision to approve the
Accreditation Commission for Health
Care, Inc., (ACHC) for continued
recognition as a national accrediting
organization for home health agencies
(HHAs) that wish to participate in the
Medicare or Medicaid programs. An
HHA that participates in Medicaid must
also meet the Medicare conditions for
participation (CoPs) as required under
42 CFR 488.6(b).
DATES: This final notice is effective
February 24, 2015 through February 24,
2021.
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Cindy Melanson, (410) 786–0310, or
Patricia Chmielewski, (410) 786–6899.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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A healthcare provider may enter into
an agreement with Medicare to
participate in the program as a HHA
provided certain requirements are met.
Sections 1861(o) and 1891 of the Social
Security Act (the Act), establish distinct
criteria for facilities seeking designation
as a HHA. Regulations concerning
Medicare provider agreements in
general are at 42 CFR part 489 and those
pertaining to the survey and
certification for Medicare participation
of providers and certain types of
suppliers are at part 488. The
regulations at part 484 specify the
specific conditions that a provider must
meet to participate in the Medicare
program as an HHA.
Generally, to enter into a Medicare
provider agreement, a facility must first
be certified as complying with the
conditions set forth in part 484 and
recommended to us for participation by
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[Federal Register Volume 80, Number 12 (Tuesday, January 20, 2015)]
[Notices]
[Pages 2707-2708]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-00802]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the Office of Research Integrity
(ORI) has taken final action in the following case:
Bin Kang, Ph.D., Oklahoma Medical Research Foundation: Based on the
Respondent's admission, an assessment conducted by the Oklahoma Medical
Research Foundation (OMRF), and additional analysis conducted by ORI in
its oversight review, ORI found that Dr. Bin Kang, Postdoctoral Fellow,
Immunobiology and Cancer Research Program, OMRF, engaged in research
misconduct in research supported by National Institute of Allergy and
Infectious Diseases (NIAID), National Institutes of Health (NIH),
grants AI056129 and AI104057.
ORI and OMRF found that Respondent engaged in research misconduct
by reporting falsified data in:
``Asb2 regulates the activity of SCF E3 ubiquitin ligases
by antagonizing CAND1-mediated exchange of F-box proteins,'' submitted
to Molecular Cell on June 26, 2014; hereafter referred to as the
``original Molecular Cell manuscript''
[[Page 2708]]
the revised version of ``Asb2 regulates the activity of
SCF E3 ubiquitin ligases by antagonizing CAND1-mediated exchange of F-
box proteins,'' submitted to Molecular Cell on September 29, 2014;
hereafter referred to as the ``revised Molecular Cell manuscript
grant application CA189216-01 submitted to the National
Cancer Institute (NCI), NIH; hereafter referred to as the ``original
NCI grant application''
grant application CA189216-01A1 submitted to NCI, NIH;
hereafter referred to as the ``revised NCI grant application''
ORI found that Respondent knowingly falsified and/or fabricated
Western blot gel images by duplication, reuse and relabeling, and/or
alteration through contrast, rotation, and/or scale of the images.
Specifically, Respondent included falsified images in all of the
figures (Figures 1-6 and S1-5) in the original Molecular Cell
manuscript, all of the figures (Figures 1-6 and S1-7) in the revised
Molecular Cell manuscript, Figures 2-4, 9, and 11 in the original
NCI grant application, and Figures 3-5, 10, and 11 in the revised NCI
grant application.
Dr. Kang has entered into a Voluntary Settlement Agreement
(Agreement) and has voluntarily agreed for a period of three (3) years,
beginning on December 23, 2014:
(1) To have his research supervised; Respondent agreed to ensure
that prior to the submission of an application for U.S. Public Health
Service (PHS) support for a research project on which the Respondent's
participation is proposed and prior to Respondent's participation in
any capacity on PHS-supported research, the institution employing him
must submit a plan for supervision of his duties to ORI for approval;
the plan for supervision must be designed to ensure the scientific
integrity of Respondent's research contribution; Respondent agreed that
he will not participate in any PHS-supported research until such a
supervision plan is submitted to and approved by ORI; Respondent agreed
to maintain responsibility for compliance with the agreed upon plan for
supervision;
(2) that any institution employing him must submit, in conjunction
with each application for PHS funds, or report, manuscript, or abstract
involving PHS- supported research in which Respondent is involved, a
certification to ORI that the data provided by Respondent are based on
actual experiments or are otherwise legitimately derived and that the
data, procedures, and methodology are accurately reported in the
application, report, manuscript, or abstract; and
(3) to exclude himself voluntarily from serving in any advisory
capacity to PHS including, but not limited to, service on any PHS
advisory committee, board, and/or peer review committee, or as a
consultant.
FOR FURTHER INFORMATION CONTACT: Acting Director, Office of Research
Integrity, 1101 Wootton Parkway, Suite 750, Rockville, MD 20852, (240)
453-8200.
Donald Wright,
Acting Director, Office of Research Integrity.
[FR Doc. 2015-00802 Filed 1-16-15; 8:45 am]
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