Findings of Research Misconduct, 15851-15852 [2018-07521]
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Federal Register / Vol. 83, No. 71 / Thursday, April 12, 2018 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
National Advisory Council on Migrant
Health
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services (HHS).
ACTION: Notice of meeting.
AGENCY:
In accordance with the
Federal Advisory Committee Act, notice
is hereby given that a National Advisory
Council on Migrant Health (NACMH)
meeting has been scheduled. This
meeting will be open to the public. The
agenda for the NACMH meeting can be
obtained by contacting the Designated
Federal Officer (DFO) or accessing the
NACMH website: https://bphc.hrsa.gov/
qualityimprovement/strategic
partnerships/nacmh/.
DATES: The meeting will be held on May
8, 2018, 8:30 a.m.–5:30 p.m., and May
9, 2018, 9:30 a.m.–5:30 p.m.
ADDRESSES: The address for the meeting
is Holiday Inn Downtown Yakima, 802
East Yakima Ave., Yakima, WA 98901.
Phone Number: 509–494–7000.
FOR FURTHER INFORMATION CONTACT: All
requests for information regarding the
NACMH should be sent to Esther Paul,
DFO, NACMH, HRSA, in one of three
ways: (1) Send a request to the following
address: Esther Paul, Office of Policy
and Program Development, Bureau of
Primary Health Care, HRSA, 5600
Fishers Lane, 16N38B, Rockville,
Maryland 20857; (2) call (301) 594–
4300; or (3) send an email to epaul@
hrsa.gov.
SUMMARY:
The
NACMH is a non-discretionary advisory
body mandated by the Public Health
Service Act (PHSA), Title 42 U.S.C. 218,
to advise, consult with, and make
recommendations to the Secretary of
HHS and the Administrator of HRSA
regarding the organization, operation,
selection, and funding of migrant health
centers and other entities funded under
section 330(g) of the PHSA (42 U.S.C.
254b). The Charter requires NACMH to
meet at least twice per year to discuss
services and issues related to the health
of migrant and seasonal agricultural
workers and their families and to
formulate their recommendations to the
HHS Secretary and HRSA
Administrator.
Agenda: The agenda includes an
overview of NACMH’s general business
activities. NACMH will also hear
presentations from a Federal official and
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SUPPLEMENTARY INFORMATION:
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experts on issues facing agricultural
workers, including the status of
agricultural worker health at the local
and national levels. Topics addressed at
this meeting include:
I. Migrant and Seasonal Agricultural
Worker Regional Health Issues/Trends;
and
II. Occupational and Environmental
Hazards and Injuries Impacting Migrant
and Seasonal Agricultural Worker
Health.
In addition, NACMH will hold a
session where migratory and seasonal
agricultural workers will comment on
matters affecting the health of migratory
and seasonal agricultural workers. This
session is scheduled for Tuesday, May
8, 2018, from 1:30 p.m. to 5:00 p.m. at
the Holiday Inn Downtown Yakima,
Yakima, WA. Agenda items are subject
to change as priorities dictate.
Members of the public will not be
able to provide oral comments during
the meeting. Written questions or
comments for the NACMH may be sent
to the DFO by April 24, 2018, using the
address and phone number provided
above. Individuals who plan to attend
the meeting and need special assistance,
such as sign language interpretation or
other reasonable accommodations,
should notify the DFO at least 10 days
prior to the meeting.
Dated: April 6, 2018.
Lori Roche,
Acting Deputy Director, Division of the
Executive Secretariat.
[FR Doc. 2018–07523 Filed 4–11–18; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
Findings of research
misconduct have been made on the part
of Brandi M. Baughman, Ph.D.,
postdoctoral fellow in the Center for
Integrative Chemical Biology and Drug
Discovery, Division of Chemical Biology
and Medicinal Chemistry, University of
North Carolina at Chapel Hill (UNC). Dr.
Baughman engaged in research
misconduct in research supported by
National Institute of General Medical
Sciences (NIGMS), National Institutes of
Health (NIH), grant R01 GM100919. The
administrative actions, including
debarment for a period of two (2) years,
were implemented beginning on March
19, 2018, and are detailed below.
SUMMARY:
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15851
FOR FURTHER INFORMATION CONTACT:
Wanda K. Jones, Dr. P.H., Interim
Director, Office of Research Integrity,
1101 Wootton Parkway, Suite 750,
Rockville, MD 20852, (240) 453–8200.
SUPPLEMENTARY INFORMATION: Notice is
hereby given that the Office of Research
Integrity (ORI) has taken final action in
the following case:
Brandi M. Baughman, Ph.D.,
University of North Carolina at Chapel
Hill: Based on an assessment conducted
by UNC, Respondent’s admission, and
analysis conducted by ORI in its
oversight review, ORI found that Dr.
Baughman, postdoctoral fellow in the
Center for Integrative Chemical Biology
and Drug Discovery, Division of
Chemical Biology and Medicinal
Chemistry, UNC, engaged in research
misconduct in research supported by
NIGMS, NIH, grant R01 GM100919. A
previous notice of research misconduct
findings based on Respondent’s prior
admission (Fed. Reg. 82(117):28078–
28079, 2017 July 20) included eleven
(11) figures in PLoS One
11(10):e0164378, 2016 in research
supported by the National Institute of
Environmental and Health Sciences
(NIEHS), NIH, and the National Institute
of Diabetes and Digestive and Kidney
Diseases (NIDDK), NIH. The Respondent
has signed a statement confirming that
she committed no additional instances
of data manipulation.
ORI found that Respondent engaged
in research misconduct by falsifying
data that were included in the first
submission of a manuscript to ACS
Chem. Biol. (hereafter referred to as the
‘‘Manuscript’’) and in the final
published version: Baughman, B.M.,
Pattenden, S.G., Norris, J.L., James, L.I.,
& Frye, S.V. ‘‘The L3MBTL3 methyllysine reader domain functions as a
dimer.’’ ACS Chem. Biol. 11:722–728,
2016 (hereafter referred to as ‘‘ACS
2016’’). The paper was retracted in: ACS
Chem. Biol. 13(1):281, 2018 Jan 19.
Respondent falsely reused and
relabeled 14 individual Western blot
images from an unrelated experiment
conducted in September 2013 showing
pulldown with biotin-UNC1215 using
0401 and HeLa overexpressed FL
L3MBTL3 lysates (hereafter referred to
as the ‘‘9/13 experiment’’) to falsely
represent Western blot analysis of
GFP.Flag co-IP experiments in GFP–WT
lysates in Figure 3 of the Manuscript
and a supplementary analysis of co-IPs
with FullL–D274A in Figure 6 of ASC
2016. Specifically, Respondent used
Western blot band images from:
• Lanes 3 and 4 (GFP input and GFP
Bn-1215 IP; 9/13 experiment) to
represent:
E:\FR\FM\12APN1.SGM
12APN1
sradovich on DSK3GMQ082PROD with NOTICES
15852
Federal Register / Vol. 83, No. 71 / Thursday, April 12, 2018 / Notices
Æ Lanes 1 and 2 (GFP:FLAG co-IP
experiments in 3MBT–GFP lysates in
the presence or absence of D381A;
Figure 3, Manuscript)
Æ N = 3 in Figure S6, ACS 2016
• Lanes 5 and 6 (GFP/Flag Input and
GFP/FlagIP; 9/13 experiment) to
represent:
Æ Lanes 3 and 4 (GFP:Flag co-IP
experiments in FL–GFP–WT lysates;
Figure 3, Manuscript)
Æ N = 1 in Figure S6, ACS 2016
• Lanes 9 and 10 (mCherry input and
mCherry Bn-1215 IP; 9/13 experiment)
to represent:
Æ Lanes 5 and 6 (GFP:FLAG co-IP
experiments in FL–GFP lysates in the
presence or absence of D381A; Figure 3,
Manuscript)
• Lanes 11 and 12 (mCherry/Flag
input and mCherry/Flag IP; 9/13
experiment) to represent:
Æ Lanes 7 and 8 (GFP:FLAG co-IP
experiments in FL–GFP WT lysates;
Figure 3, Manuscript)
• lanes 13 and 14 (mCherry/Flag IP
unbound and mCherry/Flag BN–1215;
9/13 experiment) to represent:
Æ Lanes 9 and 10 (GFP:FLAG co-IP
experiments in FL–GFP lysates in the
presence or absence of D274A; Figure 3,
manuscript
Æ N = 2 in Figure S6, ACS 2016
Dr. Baughman entered into a
Voluntary Exclusion Agreement. The
following administrative actions have
been implemented for a period of two
(2) years, beginning on March 19, 2018:
(1) Because Dr. Baughman knew when
she signed the 2017 Agreement with
ORI that there was an additional paper
with falsified figures, she agreed to
exclude herself voluntarily from any
contracting or subcontracting with any
agency of the United States Government
and from eligibility or involvement in
nonprocurement programs of the United
States Government referred to as
‘‘covered transactions’’ pursuant to
HHS’ Implementation (2 CFR part 376)
of OMB Guidelines to Agencies on
Governmentwide Debarment and
Suspension, 2 CFR part 180 (collectively
the ‘‘Debarment Regulations’’); this
Agreement supersedes the terms of the
previous supervision Agreement that
included three (3) years of research
supervision, which began on May 17,
2017; and
(2) Dr. Baughman agreed to exclude
herself voluntarily from serving in any
advisory capacity to the U.S. Public
Health Service (PHS) including, but not
limited to, service on any PHS advisory
VerDate Sep<11>2014
19:20 Apr 11, 2018
Jkt 244001
committee, board, and/or peer review
committee, or as a consultant.
Wanda K. Jones,
Interim Director, Office of Research Integrity.
[FR Doc. 2018–07521 Filed 4–11–18; 8:45 am]
BILLING CODE 4150–31–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0391]
Agency Information Collection
Request; 60-Day Public Comment
Request
Office of the Secretary, HHS
Notice.
AGENCY:
ACTION:
In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be
received on or before June 11, 2018.
ADDRESSES: Submit your comments to
Sherrette.Funn@hhs.gov or by calling
(202) 795–7714.
FOR FURTHER INFORMATION CONTACT:
When submitting comments or
requesting information, please include
the document identifier 0990–0391 and
project title for reference, to
Sherrette.funn@hhs.gov, or call the
Reports Clearance Officer.
SUPPLEMENTARY INFORMATION: Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
Title of the Collection: Hospital
Preparedness Program Data Collection.
Type of Collection: Extension.
OMB Number: 0990–0391—Hospital
Preparedness Program (HPP) within the
Division of National Healthcare
Preparedness Programs (NHPP).
Abstract: The Hospital Preparedness
Program (HPP) within the Division of
National Healthcare Preparedness
Programs (NHPP), in the Office of
Emergency Management (OEM), Office
of Assistant Secretary for Preparedness
SUMMARY:
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and Response (ASPR), in the
Department of Health and Human
Services is seeking clearance by the
Office of Management of Budget (OMB)
for an extension on Generic Data
Collection Form. The Generic Data
Collection Form will serve as the
foundation for assessment and
evaluation for HPP stakeholders,
recipients, and sub-recipient programs
and performance under the HPP
Cooperative Agreement (CA) Program.
Program data are gathered from
recipients for both ad-hoc episodic
reporting as well as required reporting
as part of the HPP Cooperative
Agreement. Ad-hoc reporting includes
but is not limited to Coalition
Assessment Tool (CAT) Data Collection
Tool, Impact Survey, HPP Partner
Survey, CA after action reports, Ebola
and Other Special Pathogens. Required
reporting include: Mid-Year and End-ofYear Progress Reports and other similar
information collections (ICs) that
account for recipient spending and
program performance on all activities
conducted in pursuit of achieving the
HPP Cooperative Agreement goals.
As part of its health care sector
preparedness and response obligations,
HPP actively collaborates with The
Centers for Disease Control and
Prevention (CDC) Public Health
Emergency Preparedness (PHEP)
Program in order to realize health care
preparedness and response goals. As
part of the HPP Cooperative Agreement,
the HPP data collection supports the
U.S. public health and health care
systems’ ability to prepare for and to
respond effectively to public health
emergencies within the United States
and associated territories and freely
associated states. Recent public health
threats of potentially catastrophic
proportion underscore the importance
of effective planning and response
capabilities that can be applied to all
hazards. As new threats to public health
and health care emerge, ASPR must
ensure that health and medical systems
are not only integral parts of emergency
response activities but also part of
emergency preparedness planning with
all relevant partners. Increased
cooperation among responders,
including state and local public health
officials, emergency medical services
(EMS), health care coalitions (HCCs),
and private health care organizations,
ensure the nation is better prepared to
respond to all hazards. State public
health departments and the mostly
private sector health care delivery
systems are now recognized as essential
partners in emergency response and
they have increased abilities to identify
E:\FR\FM\12APN1.SGM
12APN1
Agencies
[Federal Register Volume 83, Number 71 (Thursday, April 12, 2018)]
[Notices]
[Pages 15851-15852]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-07521]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
Findings of Research Misconduct
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Findings of research misconduct have been made on the part of
Brandi M. Baughman, Ph.D., postdoctoral fellow in the Center for
Integrative Chemical Biology and Drug Discovery, Division of Chemical
Biology and Medicinal Chemistry, University of North Carolina at Chapel
Hill (UNC). Dr. Baughman engaged in research misconduct in research
supported by National Institute of General Medical Sciences (NIGMS),
National Institutes of Health (NIH), grant R01 GM100919. The
administrative actions, including debarment for a period of two (2)
years, were implemented beginning on March 19, 2018, and are detailed
below.
FOR FURTHER INFORMATION CONTACT: Wanda K. Jones, Dr. P.H., Interim
Director, Office of Research Integrity, 1101 Wootton Parkway, Suite
750, Rockville, MD 20852, (240) 453-8200.
SUPPLEMENTARY INFORMATION: Notice is hereby given that the Office of
Research Integrity (ORI) has taken final action in the following case:
Brandi M. Baughman, Ph.D., University of North Carolina at Chapel
Hill: Based on an assessment conducted by UNC, Respondent's admission,
and analysis conducted by ORI in its oversight review, ORI found that
Dr. Baughman, postdoctoral fellow in the Center for Integrative
Chemical Biology and Drug Discovery, Division of Chemical Biology and
Medicinal Chemistry, UNC, engaged in research misconduct in research
supported by NIGMS, NIH, grant R01 GM100919. A previous notice of
research misconduct findings based on Respondent's prior admission
(Fed. Reg. 82(117):28078-28079, 2017 July 20) included eleven (11)
figures in PLoS One 11(10):e0164378, 2016 in research supported by the
National Institute of Environmental and Health Sciences (NIEHS), NIH,
and the National Institute of Diabetes and Digestive and Kidney
Diseases (NIDDK), NIH. The Respondent has signed a statement confirming
that she committed no additional instances of data manipulation.
ORI found that Respondent engaged in research misconduct by
falsifying data that were included in the first submission of a
manuscript to ACS Chem. Biol. (hereafter referred to as the
``Manuscript'') and in the final published version: Baughman, B.M.,
Pattenden, S.G., Norris, J.L., James, L.I., & Frye, S.V. ``The L3MBTL3
methyl-lysine reader domain functions as a dimer.'' ACS Chem. Biol.
11:722-728, 2016 (hereafter referred to as ``ACS 2016''). The paper was
retracted in: ACS Chem. Biol. 13(1):281, 2018 Jan 19.
Respondent falsely reused and relabeled 14 individual Western blot
images from an unrelated experiment conducted in September 2013 showing
pulldown with biotin-UNC1215 using 0401 and HeLa overexpressed FL
L3MBTL3 lysates (hereafter referred to as the ``9/13 experiment'') to
falsely represent Western blot analysis of GFP.Flag co-IP experiments
in GFP-WT lysates in Figure 3 of the Manuscript and a supplementary
analysis of co-IPs with FullL-D274A in Figure 6 of ASC 2016.
Specifically, Respondent used Western blot band images from:
Lanes 3 and 4 (GFP input and GFP Bn-1215 IP; 9/13
experiment) to represent:
[[Page 15852]]
[cir] Lanes 1 and 2 (GFP:FLAG co-IP experiments in 3MBT-GFP lysates
in the presence or absence of D381A; Figure 3, Manuscript)
[cir] N = 3 in Figure S6, ACS 2016
Lanes 5 and 6 (GFP/Flag Input and GFP/FlagIP; 9/13
experiment) to represent:
[cir] Lanes 3 and 4 (GFP:Flag co-IP experiments in FL-GFP-WT
lysates; Figure 3, Manuscript)
[cir] N = 1 in Figure S6, ACS 2016
Lanes 9 and 10 (mCherry input and mCherry Bn-1215 IP; 9/13
experiment) to represent:
[cir] Lanes 5 and 6 (GFP:FLAG co-IP experiments in FL-GFP lysates
in the presence or absence of D381A; Figure 3, Manuscript)
Lanes 11 and 12 (mCherry/Flag input and mCherry/Flag IP;
9/13 experiment) to represent:
[cir] Lanes 7 and 8 (GFP:FLAG co-IP experiments in FL-GFP WT
lysates; Figure 3, Manuscript)
lanes 13 and 14 (mCherry/Flag IP unbound and mCherry/Flag
BN-1215; 9/13 experiment) to represent:
[cir] Lanes 9 and 10 (GFP:FLAG co-IP experiments in FL-GFP lysates
in the presence or absence of D274A; Figure 3, manuscript
[cir] N = 2 in Figure S6, ACS 2016
Dr. Baughman entered into a Voluntary Exclusion Agreement. The
following administrative actions have been implemented for a period of
two (2) years, beginning on March 19, 2018:
(1) Because Dr. Baughman knew when she signed the 2017 Agreement
with ORI that there was an additional paper with falsified figures, she
agreed to exclude herself voluntarily from any contracting or
subcontracting with any agency of the United States Government and from
eligibility or involvement in nonprocurement programs of the United
States Government referred to as ``covered transactions'' pursuant to
HHS' Implementation (2 CFR part 376) of OMB Guidelines to Agencies on
Governmentwide Debarment and Suspension, 2 CFR part 180 (collectively
the ``Debarment Regulations''); this Agreement supersedes the terms of
the previous supervision Agreement that included three (3) years of
research supervision, which began on May 17, 2017; and
(2) Dr. Baughman agreed to exclude herself voluntarily from serving
in any advisory capacity to the U.S. Public Health Service (PHS)
including, but not limited to, service on any PHS advisory committee,
board, and/or peer review committee, or as a consultant.
Wanda K. Jones,
Interim Director, Office of Research Integrity.
[FR Doc. 2018-07521 Filed 4-11-18; 8:45 am]
BILLING CODE 4150-31-P