R.W. Stottmann: search on Z-Library

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1

Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants

Snedeker, John, Gibbons, William J., Paulding, David F., Abdelhamed, Zakia, Prows, Daniel R., Stottmann, Rolf W., Cox, Gregory A.

Journal:

Year:

2019

Language:

english

File:

PDF, 8.28 MB

english, 2019

2

Bone morphogenetic protein signaling is required in the dorsal neural folds before neurulation for the induction of spinal neural crest cells and dorsal neurons

Rolf W. Stottmann, John Klingensmith

Journal:

Developmental Dynamics

Year:

2011

Language:

english

File:

PDF, 2.41 MB

english, 2011

3

A mutation in Ccdc39 causes neonatal hydrocephalus with abnormal motile cilia development in mice

Abdelhamed, Zakia, Vuong, Shawn M., Hill, Lauren, Shula, Crystal, Timms, Andrew, Beier, David, Campbell, Kenneth, Mangano, Francesco T., Stottmann, Rolf W., Goto, June

Journal:

Development (The Company of Biologists)

Year:

2018

Language:

english

File:

PDF, 13.45 MB

english, 2018

4

Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression

Jeruschke, Stefanie, Jeruschke, Kay, DiStasio, Andrew, Karaterzi, Sinem, Büscher, Anja K., Nalbant, Perihan, Klein-Hitpass, Ludger, Hoyer, Peter F., Weiss, Jürgen, Stottmann, Rolf W., Weber, Stefanie,

Journal:

Year:

2015

Language:

english

File:

PDF, 13.07 MB

english, 2015

5

Differential requirements of tubulin genes in mammalian forebrain development

Bittermann, Elizabeth, Abdelhamed, Zakia, Liegel, Ryan P., Menke, Chelsea, Timms, Andrew, Beier, David R., Stottmann, Rolf W., Moore, Jeffrey

Journal:

Year:

2019

Language:

english

File:

PDF, 23.07 MB

english, 2019

6

ZNF423 patient variants, truncations, and in-frame deletions in mice define an allele-dependent range of midline brain abnormalities

Deshpande, Ojas, Lara, Raquel Z., Zhang, Oliver R., Concepcion, Dorothy, Hamilton, Bruce A., Stottmann, Rolf W.

Journal:

Year:

2020

File:

PDF, 19.31 MB

2020

7

Distribution of TAG-1 and synaptophysin in the developing cerebellar cortex: Relationship to Purkinje cell dendritic development

Stottmann, Rolf W., Rivas, Rodolfo J.

Journal:

The Journal of Comparative Neurology

Year:

1998

Language:

english

File:

PDF, 2.04 MB

english, 1998

8

Endogenous bone morphogenetic protein antagonists regulate mammalian neural crest generation and survival

Ryan M. Anderson, Rolf W. Stottmann, Murim Choi, John Klingensmith

Journal:

Developmental Dynamics

Year:

2006

Language:

english

File:

PDF, 1.46 MB

english, 2006

9

Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse

R.W. Stottmann, B.C. Bjork, J.B. Doyle, D.R. Beier

Journal:

Year:

2010

Language:

english

File:

PDF, 3.01 MB

english, 2010

10

Continuous-time simulation of metal cutting on a lathe

Thomas L. Ward, Patricia A.S. Ralston, Denise J.C. Stottmann

Journal:

Computers & Industrial Engineering

Year:

1991

Language:

english

File:

PDF, 582 KB

english, 1991

11

SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs

Wesley A. Beckstead, Bryan C. Bjork, Rolf W. Stottmann, Shamil Sunyaev, David R. Beier

Journal:

Mammalian Genome

Year:

2008

Language:

english

File:

PDF, 190 KB

english, 2008

12

THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia

Haycraft, Courtney J, Besschetnova, Tatiana Y, Turbe-Doan, Annick, Stottmann, Rolf W, Herron, Bruce J, Chesebro, Allyson L, Qiu, Haiyan, Scherz, Paul J, Shah, Jagesh V, Tran, Pamela V

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 798 KB

english, 2008

13

Mutation mapping and identification by whole-genome sequencing

Leshchiner, I., Alexa, K., Kelsey, P., Adzhubei, I., Austin-Tse, C. A., Cooney, J. D., Anderson, H., King, M. J., Stottmann, R. W., Garnaas, M. K., Ha, S., Drummond, I. A., Paw, B. H., North, T. E., B

Journal:

Genome Research

Year:

2012

Language:

english

File:

PDF, 1.00 MB

english, 2012

14

The BMP Antagonists Chordin and Noggin Have Essential but Redundant Roles in Mouse Mandibular Outgrowth

Rolf W. Stottmann, Ryan M. Anderson, John Klingensmith

Journal:

Developmental Biology

Year:

2001

Language:

english

File:

PDF, 615 KB

english, 2001

15

The BMP antagonist Noggin promotes cranial and spinal neurulation by distinct mechanisms

Rolf W. Stottmann, Mark Berrong, Karen Matta, Murim Choi, John Klingensmith

Journal:

Developmental Biology

Year:

2006

Language:

english

File:

PDF, 1.19 MB

english, 2006

16

An ENU screen for novel genes required in mammalian forebrain development

Rolf W. Stottmann, Yujuan Yun, David Beier

Journal:

Developmental Biology

Year:

2007

Language:

english

File:

PDF, 47 KB

english, 2007

17

Mouse mutagenesis for targeting mutations causing abnormal diaphragm development

Kate G. Ackerman, Rolf W. Stottmann, Yujuan Yun, Liqing Luo, Andrew Bolton, Jennifer L. Moran, R. Beier

Journal:

Developmental Biology

Year:

2007

Language:

english

File:

PDF, 69 KB

english, 2007

18

An Enu screen reveals novel genes required for mammalian forebrain development

Rolf W. Stottmann, Yujuan Yun, David Beier

Journal:

Developmental Biology

Year:

2008

Language:

english

File:

PDF, 118 KB

english, 2008

19

An ENU screen reveals novel genes in mammalian forebrain development

Rolf W. Stottmann, Annick Turbe-Doan, Haiyan Qui, David Beier

Journal:

Developmental Biology

Year:

2009

Language:

english

File:

PDF, 53 KB

english, 2009

20

Ttc21b is required to restrict sonic hedgehog activity in the developing mouse forebrain

R.W. Stottmann, P.V. Tran, A. Turbe-Doan, D.R. Beier

Journal:

Developmental Biology

Year:

2009

Language:

english

File:

PDF, 7.27 MB

english, 2009

21

Conservation and regulatory associations of a wide affinity range of mouse transcription factor binding sites

Savina A. Jaeger, Esther T. Chan, Michael F. Berger, Rolf Stottmann, Timothy R. Hughes, Martha L. Bulyk

Journal:

Year:

2010

Language:

english

File:

PDF, 1.60 MB

english, 2010

22

ENU mutagenesis identifies novel genes required for forebrain development

Rolf W. Stottmann, David Beier

Journal:

Developmental Biology

Year:

2011

Language:

english

File:

PDF, 46 KB

english, 2011

23

Toward a systems-level understanding of the Hedgehog signaling pathway: defining the complex, robust, and fragile

Tran, Pamela V., Lachke, Salil A., Stottmann, Rolf W.

Journal:

Wiley Interdisciplinary Reviews: Systems Biology and Medicine

Year:

2013

Language:

english

File:

PDF, 332 KB

english, 2013

24

A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse

Stottmann, R. W., Donlin, M., Hafner, A., Bernard, A., Sinclair, D. A., Beier, D. R.

Journal:

Human Molecular Genetics

Year:

2013

Language:

english

File:

PDF, 1.01 MB

english, 2013

25

[Methods in Enzymology] Guide to Techniques in Mouse Development, Part B: Mouse Molecular Genetics, 2nd Edition Volume 477 || Using ENU Mutagenesis for Phenotype-Driven Analysis of the Mouse

Stottmann, Rolf W.

Year:

2010

Language:

english

File:

PDF, 229 KB

english, 2010

26

A Novel Mutation in the Gene Encoding Noggin is Not Causative in Human Neural Tube Defects

BAUER, KIM A., GEORGE, TIMOTHY M., ENTERLINE, DAVID S., STOTTMANN, ROLF W., MELVIN, ELIZABETH C., SIEGEL, DEBORAH, SAMAL, SUREKHA, HAUSER, MICHAEL A., KLINGENSMITH, JOHN, NYE, JEFFERY S., SPEER, MARCY

Journal:

Journal of Neurogenetics

Year:

2002

Language:

english

File:

PDF, 184 KB

english, 2002

27

A Novel Mutation in the Gene Encoding Noggin is Not Causative in Human Neural Tube Defects

BAUER, KIM A., GEORGE, TIMOTHY M., ENTERLINE, DAVID S., STOTTMANN, ROLF W., MELVIN, ELIZABETH C., SIEGEL, DEBORAH, SAMAL, SUREKHA, HAUSER, MICHAEL A., KLINGENSMITH, JOHN, NYE, JEFFERY S., SPEER, MARCY

Journal:

Journal of Neurogenetics

Year:

2002

Language:

english

File:

PDF, 184 KB

english, 2002

28

A Novel Mutation in the Gene Encoding Noggin is Not Causative in Human Neural Tube Defects

BAUER, KIM A., GEORGE, TIMOTHY M., ENTERLINE, DAVID S., STOTTMANN, ROLF W., MELVIN, ELIZABETH C., SIEGEL, DEBORAH, SAMAL, SUREKHA, HAUSER, MICHAEL A., KLINGENSMITH, JOHN, NYE, JEFFERY S., SPEER, MARCY

Journal:

Journal of Neurogenetics

Year:

2002

Language:

english

File:

PDF, 184 KB

english, 2002

29

A mutation in FRIZZLED2 impairs Wnt signaling and causes autosomal dominant omodysplasia

Saal, H. M., Prows, C. A., Guerreiro, I., Donlin, M., Knudson, L., Sund, K. L., Chang, C.-F., Brugmann, S. A., Stottmann, R. W.

Journal:

Human Molecular Genetics

Year:

2015

Language:

english

File:

PDF, 651 KB

english, 2015

30

BMP receptor IA is required in mammalian neural crest cells for development of the cardiac outflow tract and ventricular myocardium

Stottmann, R. W.

Journal:

Development (The Company of Biologists)

Year:

2004

Language:

english

File:

PDF, 823 KB

english, 2004

31

Focusing Forward Genetics: A Tripartite ENU Screen for Neurodevelopmental Mutations in the Mouse

Stottmann, R. W., Moran, J. L., Turbe-Doan, A., Driver, E., Kelley, M., Beier, D. R.

Journal:

Year:

2011

Language:

english

File:

PDF, 1.20 MB

english, 2011

32

The Bone Morphogenetic Protein Antagonist Noggin Regulates Mammalian Cardiac Morphogenesis

Choi, M., Stottmann, R. W., Yang, Y.-P., Meyers, E. N., Klingensmith, J.

Journal:

Circulation Research

Year:

2007

Language:

english

File:

PDF, 1.21 MB

english, 2007

33

Cholesterol Metabolism Is Required for Intracellular Hedgehog Signal Transduction In Vivo

Stottmann, Rolf W., Turbe-Doan, Annick, Tran, Pamela, Kratz, Lisa E., Moran, Jennifer L., Kelley, Richard I., Beier, David R., Barsh, Gregory S.

Journal:

Year:

2011

Language:

english

File:

PDF, 3.09 MB

english, 2011

34

Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain

Driver, Ashley M., Kratz, Lisa E., Kelley, Richard I., Stottmann, Rolf W.

Journal:

Neurobiology of Disease

Year:

2016

Language:

english

File:

PDF, 1.50 MB

english, 2016

35

WITHDRAWN: Mouse mutagenesis for targeting mutations causing abnormal diaphragm development

Bolton, Andrew, Moran, Jennifer L., Ackerman, Kate G., Luo, Liqing, Beier, R., Stottmann, Rolf W., Yun, Yujuan

Journal:

Developmental Biology

Year:

2007

File:

PDF, 10 KB

2007

36

Novel genetic tools facilitate the study of cortical neuron migration

Cionni, Megan, Menke, Chelsea, Stottmann, Rolf W.

Journal:

Mammalian Genome

Year:

2016

Language:

english

File:

PDF, 4.44 MB

english, 2016

37

Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development

Menke, Chelsea, Cionni, Megan, Siggers, Trevor, Bulyk, Martha L., Beier, David R., Stottmann, Rolf W.

Journal:

Year:

2015

Language:

english

File:

PDF, 521 KB

english, 2015

38

A heterozygous mutation in tubulin, beta 2B ( Tubb2b ) causes cognitive deficits and hippocampal disorganization

Stottmann, Rolf W., Driver, Ashley, Gutierrez, Arnold, Skelton, Matthew R., Muntifering, Michael, Stepien, Christopher, Knudson, Luke, Kofron, Matthew, Vorhees, Charles V., Williams, Michael T.

Journal:

Genes, Brain and Behavior

Year:

2016

Language:

english

File:

PDF, 1.23 MB

english, 2016

39

The Mouse MC13 Mutant Is a Novel ENU Mutation in Collagen Type II, Alpha 1

Cionni, Megan, Menke, Chelsea, Stottmann, Rolf W., Silver, Debra L.

Journal:

Year:

2014

Language:

english

File:

PDF, 620 KB

english, 2014

40

Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development

Snedeker, John, Schock, Elizabeth N., Struve, Jamie N., Chang, Ching-Fang, Cionni, Megan, Tran, Pamela V., Brugmann, Samantha A., Stottmann, Rolf W., Stieger, Knut

Journal:

Year:

2017

Language:

english

File:

PDF, 3.38 MB

english, 2017

41

Congenital Cataracts and Gut Dysmotility in a DYNC1H1 Dyneinopathy Patient

Gelineau-Morel, Rose, Lukacs, Marshall, Weaver, K., Hufnagel, Robert, Gilbert, Donald, Stottmann, Rolf

Journal:

Year:

2016

Language:

english

File:

PDF, 1.14 MB

english, 2016

42

Ttc21b Is Required in Bergmann Glia for Proper Granule Cell Radial Migration

Driver, Ashley, Shumrick, Christopher, Stottmann, Rolf

Journal:

Journal of Developmental Biology

Year:

2017

Language:

english

File:

PDF, 3.98 MB

english, 2017

43

Using human sequencing to guide craniofacial research

Liegel, Ryan P., Finnerty, Erin, Ward, Lauren, DiStasio, Andrew, Hufnagel, Robert B., Saal, Howard M., Sund, Kristen L., Prows, Cynthia A., Stottmann, Rolf

Journal:

Year:

2018

Language:

english

File:

PDF, 1.58 MB

english, 2018

44

Severe biallelic loss-of-function mutations in nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) in two fetuses with fetal akinesia deformation sequence

Lukacs, Marshall, Gilley, Jonathan, Zhu, Yi, Orsomando, Giuseppe, Angeletti, Carlo, Liu, Jiaqi, Yang, Xiuna, Park, Joun, Hopkin, Robert J., Coleman, Michael P., Zhai, R. Grace, Stottmann, Rolf W.

Journal:

Experimental Neurology

Year:

2019

Language:

english

File:

PDF, 1.81 MB

english, 2019

45

Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants

Snedeker, John, Gibbons, William J., Paulding, David F., Abdelhamed, Zakia, Prows, Daniel R., Stottmann, Rolf W., Cox, Gregory A.

Journal:

Year:

2019

File:

PDF, 8.28 MB

2019

46

CNS glycosylphosphatidylinositol deficiency results in delayed white matter development, ataxia and premature death in a novel mouse model

Lukacs, Marshall, Blizzard, Lauren E, Stottmann, Rolf W

Journal:

Human Molecular Genetics

Year:

2020

File:

PDF, 1.76 MB

2020

47

Mandibulofacial dysostosis with microcephaly: An expansion of the phenotype via parental survey

Abell, Katherine, Hopkin, Robert J., Bender, Patricia L., Jackson, Farrah, Smallwood, Kelly, Sullivan, Bonnie, Stottmann, Rolf W., Saal, Howard M., Weaver, K. Nicole

Journal:

American Journal of Medical Genetics Part A

Year:

2020

File:

PDF, 1.86 MB

2020