Michael F. Wangler: search on Z-Library

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1

Inborn Errors of Metabolism Involving Complex Molecules

Bellettato, Cinzia Maria, Hubert, Leroy, Scarpa, Maurizio, Wangler, Michael F.

Journal:

Pediatric Clinics of North America

Year:

2018

Language:

english

File:

PDF, 2.33 MB

english, 2018

2

The phenotypic spectrum of Xia-Gibbs syndrome

Jiang, Yunyun, Wangler, Michael F., McGuire, Amy L., Lupski, James R., Posey, Jennifer E., Khayat, Michael M., Murdock, David R., Sanchez-Pulido, Luis, Ponting, Chris P., Xia, Fan, Hunter, Jill V., Me

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 960 KB

english, 2018

3

68Ga-Complex Lipophilicity and the Targeting Property of a Urea-Based PSMA Inhibitor for PET Imaging

Eder, Matthias, Schäfer, Martin, Bauder-Wüst, Ulrike, Hull, William-Edmund, Wängler, Carmen, Mier, Walter, Haberkorn, Uwe, Eisenhut, Michael

Journal:

Bioconjugate Chemistry

Year:

2012

Language:

english

File:

PDF, 441 KB

english, 2012

4

Ari-1 Regulates Myonuclear Organization Together with Parkin and Is Associated with Aortic Aneurysms

Tan, Kai Li, Haelterman, Nele A., Kwartler, Callie S., Regalado, Ellen S., Lee, Pei-Tseng, Nagarkar-Jaiswal, Sonal, Guo, Dong-Chuan, Duraine, Lita, Wangler, Michael F., Bamshad, Michael J., Nickerson,

Journal:

Developmental Cell

Year:

2018

Language:

english

File:

PDF, 7.04 MB

english, 2018

5

Multimerization of cRGD Peptides by Click Chemistry: Synthetic Strategies, Chemical Limitations, and Influence on Biological Properties

Dr. Carmen Wängler , Dr. Simone Maschauer, Dr. Olaf Prante, Dipl.-Ing. Martin Schäfer, Prof. Dr. Ralf Schirrmacher, Prof. Dr. Peter Bartenstein, Prof. Dr. Michael Eisenhut, Dr. Björn Wängler

Journal:

Year:

2010

Language:

english

File:

PDF, 1023 KB

english, 2010

6

Optimization of the felge on parallel bars

Hiley, Michael J., Wangler, Roger, Predescu, Gheorghe

Journal:

Sports Biomechanics

Year:

2009

Language:

english

File:

PDF, 1.41 MB

english, 2009

7

99mTc Complexes with activated ester functions; ligands comprising a 3,4-diamino-benzoate backbone

Osmar Calderon Sanchez, Ashour Mohammed, Claudia Bauer, Markus Wolf, Björn Wängler, Walter Mier, Uwe Haberkorn, Raoul Mocelo, Michael Eisenhut

Journal:

Nuclear Medicine and Biology

Year:

2006

Language:

english

File:

PDF, 462 KB

english, 2006

8

Dataset for a case report of a homozygous PEX16 F332del mutation

Bacino, Carlos, Chao, Yu-Hsin, Seto, Elaine, Lotze, Tim, Xia, Fan, Jones, Richard O., Moser, Ann, Wangler, Michael F.

Journal:

Year:

2016

Language:

english

File:

PDF, 1.36 MB

english, 2016

9

Internetassoziierte Gesundheitsängste in der hausärztlichen Versorgung – Ergebnisse einer Befragung unter Allgemeinmedizinern und hausärztlich tätigen Internisten in Hessen

Wangler, Julian, Jansky, Michael

Journal:

DMW - Deutsche Medizinische Wochenschrift

Year:

2019

File:

PDF, 622 KB

2019

10

Retrospective Diagnosis of Ataxia-Telangiectasia in an Adolescent Patient With a Remote History of T-Cell Leukemia

Sze, Sei-Gyung K., Lederman, Howard M., Crawford, Thomas O., Wangler, Michael F., Lewis, Andrea M., Kastan, Michael B., Dibra, Harpreet K., Taylor, Alexander M.R., Wechsler, Daniel S.

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2019

File:

PDF, 109 KB

2019

11

Digital necrosis in an infant with severe spinal muscular atrophy

Carrasco, Diana, Magoulas, Pilar, Scull, Jennifer C., Jarrell, Jill A., Lalani, Seema R., Wangler, Michael F.

Journal:

Neurology: Genetics

Year:

2019

File:

PDF, 198 KB

2019

12

Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene

Stuart W. Tompson, Carlos A. Bacino, Nicole P. Safina, Michael B. Bober, Virginia K. Proud, Tara Funari, Michael F. Wangler, Lisette Nevarez, Leena Ala-Kokko, William R. Wilcox, David R. Eyre, Deborah

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 487 KB

english, 2010

13

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: A case series of 19 patients

Aimee S. Chang, Kelle H. Moley, Michael Wangler, Andrew P. Feinberg, Michael R. DeBaun

Journal:

Fertility and Sterility

Year:

2005

Language:

english

File:

PDF, 92 KB

english, 2005

14

General practitionersâ challenges and strategies in dealing with Internet-related health anxietiesâresults of aÂ qualitative study among primary care physicians in Germany; Herausforderungen fÃ¼r AllgemeinÃ¤rzte und Strategien im Umgang mit internetbedingten GesundheitsÃ¤ngsten â Ergebnisse einer qualitativen Studie bei Ãrzten der Grundversorgung in Deutschland;

Wangler, Julian, Jansky, Michael

Journal:

Wiener Medizinische Wochenschrift

Year:

2020

File:

PDF, 367 KB

2020

15

BetreuungsbedÃ¼rfnisse von Patienten mit Ãbergewicht und Adipositas in der Hausarztpraxis â Ergebnisse einer Interviewstudie; Care needs of obese patients in primary careâfindings from an interview study;

Wangler, Julian, Jansky, Michael

Journal:

Prävention und Gesundheitsförderung

Year:

2020

File:

PDF, 370 KB

2020

16

Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines

Braverman, Nancy E., Raymond, Gerald V., Rizzo, William B., Moser, Ann B., Wilkinson, Mark E., Stone, Edwin M., Steinberg, Steven J., Wangler, Michael F., Rush, Eric T., Hacia, Joseph G., Bose, Mousum

Journal:

Molecular Genetics and Metabolism

Year:

2015

Language:

english

File:

PDF, 712 KB

english, 2015

17

A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers

Wangler, Michael F, Hubert, Leroy, Donti, Taraka R, Ventura, Meredith J, Miller, Marcus J, Braverman, Nancy, Gawron, Kelly, Bose, Mousumi, Moser, Ann B, Jones, Richard O, Rizzo, William B, Sutton, V R

Journal:

Genetics in Medicine

Year:

2018

Language:

english

File:

PDF, 2.05 MB

english, 2018

18

Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

Chung, Hyung-lok, Wangler, Michael F., Marcogliese, Paul C., Jo, Juyeon, Ravenscroft, Thomas A., Zuo, Zhongyuan, Duraine, Lita, Sadeghzadeh, Sina, Li-Kroeger, David, Schmidt, Robert E., Pestronk, Alan

Journal:

Year:

2020

File:

PDF, 7.80 MB

2020

19

A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease

Graves, Hillary K., Jangam, Sharayu, Tan, Kai Li, Pignata, Antonella, Seto, Elaine S., Yamamoto, Shinya, Wangler, Michael F.

Journal:

G3 Genes|Genome|Genetics

Year:

2020

File:

PDF, 2.23 MB

2020

20

The fruit fly at the interface of diagnosis and pathogenic mechanisms of rare and common human diseases

Bellen, Hugo J, Wangler, Michael F, Yamamoto, Shinya

Journal:

Human Molecular Genetics

Year:

2019

Language:

english

File:

PDF, 674 KB

english, 2019

21

An SCN1B Variant Found in a Child Diagnosed with Epilepsy and Brugada Syndrome Modifies Brain-Type (NaV1.1) and Cardiac-Type (NaV1.5) Sodium Currents

Martinez-Moreno, Rebecca, Riuró, Helena, Selga, Elisabeth, Wangler, Michael F., Brugada, Ramon, Pérez, Guillermo J., Scornik, Fabiana S.

Journal:

Biophysical Journal

Year:

2018

Language:

english

File:

PDF, 50 KB

english, 2018

22

Die Bedeutung des hausärztlichen Settings für die Bewegungs- und Gesundheitsförderung im höheren Lebensalter – Ergebnisse einer Befragung; Importance of primary care providers for promotion of exercise and health in older patients—survey results;

Wangler, Julian, Jansky, Michael

Journal:

Prävention und Gesundheitsförderung

Year:

2019

Language:

german

File:

PDF, 275 KB

german, 2019

23

Dementia diagnostics in general practitioner care; Demenzdiagnostik in der Allgemeinmedizin;

Wangler, Julian, Jansky, Michael

Journal:

Wiener Medizinische Wochenschrift

Year:

2019

File:

PDF, 343 KB

2019

24

A comparative calorimetric study on trna unfolding

Franz Joachim Schott, Michael Grubert, Wilhelm Wangler, Theodor Ackermann

Journal:

Biophysical Chemistry

Year:

1981

Language:

english

File:

PDF, 544 KB

english, 1981

25

Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum

Donti, Taraka R., Cappuccio, Gerarda, Hubert, Leroy, Neira, Juanita, Atwal, Paldeep S., Miller, Marcus J., Cardon, Aaron L., Sutton, V. Reid, Porter, Brenda E., Baumer, Fiona M., Wangler, Michael F.,

Journal:

Molecular Genetics and Metabolism Reports

Year:

2016

Language:

english

File:

PDF, 536 KB

english, 2016

26

An SCN1B Variant Found in a Child Diagnosed with Epilepsy and Brugada Syndrome Modifies Brain-Type (NaV1.1) and Cardiac-Type (NaV1.5) Sodium Currents

Martinez-Moreno, Rebecca, Riuró, Helena, Selga, Elisabeth, Wangler, Michael F., Brugada, Ramon, Pérez, Guillermo J., Scornik, Fabiana S.

Journal:

Biophysical Journal

Year:

2018

File:

PDF, 50 KB

2018

27

498: Placental pathology findings in cases of familial spontaneous preterm birth

Emily Defranco, Tammy Shen, Michael Wangler, Zachary Kistka, Lisanne Palomar, Adrienne Stormo, Jevon Plunkett, Phyllis Huettner, Louis Muglia

Journal:

American Journal of Obstetrics and Gynecology

Year:

2009

Language:

english

File:

PDF, 472 KB

english, 2009

28

Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research

Wangler, Michael F., Yamamoto, Shinya, Chao, Hsiao-Tuan, Posey, Jennifer E., Westerfield, Monte, Postlethwait, John, Hieter, Philip, Boycott, Kym M., Campeau, Philippe M., Bellen, Hugo J.

Journal:

Year:

2017

Language:

english

File:

PDF, 1.51 MB

english, 2017

29

De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures

Assia Batzir, Nurit, Bhagwat, Pranjali, Eble, Tanya, Liu, Pengfei, Eng, Christine, Elsea, Sarah H, Robak, Laurie A, Scaglia, Fernando, Goldman, Alica, Dhar, Shweta U, Wangler, Michael F

Journal:

Molecular Case Studies

Year:

2019

Language:

english

File:

PDF, 1.64 MB

english, 2019

30

Erratum: Kann ein nationales Gesundheitsportal die PrimÃ¤rversorgung unterstÃ¼tzen? â Ergebnisse einer Befragungsstudie unter HausÃ¤rzten

Wangler, Julian, Stachwitz, Philipp, Jansky, Michael

Journal:

Das Gesundheitswesen

Year:

2020

File:

PDF, 72 KB

2020

31

Decreased Mivacurium Constant Infusion Requirements with Defasciculating Doses of Pancuronium

Wangler, Michael D., Thapar, Pankaj, Skerman, Jonathan H.

Journal:

Anesthesia & Analgesia

Year:

1997

Language:

english

File:

PDF, 443 KB

english, 1997

32

Basic Science Methods for Clinical Researchers || In Vivo Animal Modeling

Wangler, Michael F.

Year:

2017

Language:

english

File:

PDF, 1.75 MB

english, 2017

33

A Mitochondrial Translation Defect Identified by Whole-Exome Sequencing Expands the Phenotypic Spectrum for MARS2

Wangler, Michael, Bayat, Vafa, Bellen, Hugo

Journal:

Year:

2015

Language:

english

File:

PDF, 76 KB

english, 2015

34

Drosophila and genome-wide association studies: a review and resource for the functional dissection of human complex traits

Wangler, Michael F., Hu, Yanhui, Shulman, Joshua M.

Journal:

Disease Models & Mechanisms

Year:

2017

Language:

english

File:

PDF, 669 KB

english, 2017

35

An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders

Martinez-Moreno, Rebecca, Selga, Elisabet, RiurÃ³, Helena, Carreras, David, Parnes, Mered, Srinivasan, Chandra, Wangler, Michael F., PÃ©rez, Guillermo J., Scornik, Fabiana S., Brugada, Ramon

Journal:

Frontiers in Cell and Developmental Biology

Year:

2020

File:

PDF, 7.60 MB

2020

36

Factors associated with preterm delivery in mothers of children with Beckwith–Wiedemann syndrome: A case cohort study from the BWS registry

Michael F. Wangler, Aimee S. Chang, Kelle H. Moley, Andrew P. Feinberg, Michael R. DeBaun

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 77 KB

english, 2005

37

Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome

Wangler, Michael F., Gonzaga-Jauregui, Claudia, Gambin, Tomasz, Penney, Samantha, Moss, Timothy, Chopra, Atul, Probst, Frank J., Xia, Fan, Yang, Yaping, Werlin, Steven, Eglite, Ieva, Kornejeva, Liene,

Journal:

Year:

2014

Language:

english

File:

PDF, 1.82 MB

english, 2014

38

MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome

Wang, Julia, Al-Ouran, Rami, Hu, Yanhui, Kim, Seon-Young, Wan, Ying-Wooi, Wangler, Michael F., Yamamoto, Shinya, Chao, Hsiao-Tuan, Comjean, Aram, Mohr, Stephanie E., Perrimon, Norbert, Liu, Zhandong,

Journal:

The American Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 642 KB

english, 2017

39

The expanding neurological phenotype of DNM1L-related disorders

Wangler, Michael F, Assia Batzir, Nurit, Robak, Laurie A, Koenig, Mary K, Bacino, Carlos A, Scaglia, Fernando, Bellen, Hugo J

Journal:

Year:

2018

Language:

english

File:

PDF, 319 KB

english, 2018

40

Application of tris-allyl-DOTA in the preparation of DOTA–peptide conjugates

Björn Wängler, Carmen Beck, Ulrike Wagner-Utermann, Esther Schirrmacher, Claudia Bauer, Frank Rösch, Ralf Schirrmacher, Michael Eisenhut

Journal:

Tetrahedron Letters

Year:

2006

Language:

english

File:

PDF, 140 KB

english, 2006

41

Silica- and Alkoxysilane-Coated Ultrasmall Superparamagnetic Iron Oxide Particles: A Promising Tool To Label Cells for Magnetic Resonance Imaging

Zhang, Chunfu, Wängler, Björn, Morgenstern, Bernd, Zentgraf, Hanswalter, Eisenhut, Michael, Untenecker, Harald, Krüger, Ralf, Huss, Ralf, Seliger, Christian, Semmler, Wolfhard, Kiessling, Fabian

Journal:

Year:

2007

Language:

english

File:

PDF, 338 KB

english, 2007

42

FIRE AND SUCCESSION IN PINYON-JUNIPER WOODLANDS OF THE SAN BERNARDINO MOUNTAINS, CALIFORNIA

Michael J. Wangler and Richard A. Minnich

Journal:

Year:

1996

Language:

english

File:

PDF, 1.94 MB

english, 1996

43

De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy

Chung, Hyung-lok, Mao, Xiao, Wang, Hua, Park, Ye-Jin, Marcogliese, Paul C., Rosenfeld, Jill A., Burrage, Lindsay C., Liu, Pengfei, Murdock, David R., Yamamoto, Shinya, Wangler, Michael F., Chao, Hsiao

Journal:

The American Journal of Human Genetics

Year:

2020

File:

PDF, 2.82 MB

2020

44

De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea

Xia, Fan, Bainbridge, Matthew N., Tan, Tiong Yang, Wangler, Michael F., Scheuerle, Angela E., Zackai, Elaine H., Harr, Margaret H., Sutton, V. Reid, Nalam, Roopa L., Zhu, Wenmiao, Nash, Margot, Ryan,

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 1.03 MB

english, 2014

45

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Harnish, J. Michael, Deal, Samantha L., Chao, Hsiao-Tuan, Wangler, Michael F., Yamamoto, Shinya

Journal:

Journal of Visualized Experiments

Year:

2019

Language:

english

File:

PDF, 818 KB

english, 2019

46

Antioxidant proteins TSA and PAG interact synergistically with Presenilin to modulate Notch signaling inDrosophila

Michael F. Wangler, Lawrence T. Reiter, Georgianna Zimm, Jennifer Trimble-Morgan, Jane Wu, Ethan Bier

Journal:

Year:

2011

Language:

english

File:

PDF, 644 KB

english, 2011

47

Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila

Chao, Yu-Hsin, Robak, Laurie A., Xia, Fan, Koenig, Mary K., Adesina, Adekunle, Bacino, Carlos A., Scaglia, Fernando, Bellen, Hugo J., Wangler, Michael F.

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 1.59 MB

english, 2016

48

Wie wirken mediale Altersbilder auf Ã¤ltere Menschen? â Ergebnisse einer Rezeptionsstudie; What effects do media-mediated images of old age have on older people?âResults of aÂ reception study;

Wangler, Julian, Jansky, Michael

Journal:

Zeitschrift für Gerontologie und Geriatrie

Year:

2020

File:

PDF, 393 KB

2020

49

Inheritance pattern of Beckwith–Wiedemann syndrome is heterogeneous in 291 families with an affected proband

Michael F. Wangler, Ping An, Andrew P. Feinberg, Michael Province, Michael R. DeBaun

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 144 KB

english, 2005

50

Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia

Liu, Jidong, Ding, Guolian, Zou, Kexin, Jiang, Ziru, Zhang, Junyu, Lu, Yunhua, Pignata, Antonella, Venner, Eric, Liu, Pengfei, Liu, Zhandong, Wangler, Michael F., Sun, Zheng

Journal:

Molecular Genetics & Genomic Medicine

Year:

2020

Language:

english

File:

PDF, 599 KB

english, 2020

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