Canlyniadau Chwilio am Awdur

1

Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes gan Colin A. Johnson

Cyhoeddwyd 2003

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Wedi'i Gadw mewn:
2

The transition zone: an essential functional compartment of cilia gan Katarzyna Szymańska, Colin A. Johnson

Cyhoeddwyd 2012

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Artigo

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3

The Cilium: Cellular Antenna and Central Processing Unit gan Jarema Malicki, Colin A. Johnson

Cyhoeddwyd 2016

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4

Ciliogenesis and the DNA damage response: a stressful relationship gan Colin A. Johnson, Spencer J. Collis

Cyhoeddwyd 2016

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5

The role of primary cilia in the development and disease of the retina gan Gabrielle Wheway, David Parry, Colin A. Johnson

Cyhoeddwyd 2013

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Wedi'i Gadw mewn:
6

Recent advances in the molecular pathology, cell biology and genetics of ciliopathies gan Matthew Adams, Ursula M. Smith, Clare V. Logan, Colin A. Johnson

Cyhoeddwyd 2008

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Wedi'i Gadw mewn:
7

Deacetylase Activity Associates with Topoisomerase II and Is Necessary for Etoposide-induced Apoptosis gan Colin A. Johnson, Kay Padget, Caroline A. Austin, Bryan M. Turner

Cyhoeddwyd 2001

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Artigo

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Wedi'i Gadw mewn:
8

Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin Please gan Claire E. L. Smith, Alice V. R. Lake, Colin A. Johnson

Cyhoeddwyd 2020

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9

Meckel–Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances gan Verity Hartill, Katarzyna Szymańska, Saghira Malik Sharif, Gabrielle Wheway, Colin A. Johnson

Cyhoeddwyd 2017

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Revisão

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Wedi'i Gadw mewn:
10

Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome gan Gabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, Carmel Toomes, Chris F. Inglehearn, Colin A. Johnson

Cyhoeddwyd 2013

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Artigo

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Wedi'i Gadw mewn:
11

Human Class I Histone Deacetylase Complexes Show Enhanced Catalytic Activity in the Presence of ATP and Co-immunoprecipitate with the ATP-dependent Chaperone Protein Hsp70 gan Colin A. Johnson, Darren A. White, Jayne S. Lavender, Laura P. O’Neill, Bryan M. Turner

Cyhoeddwyd 2002

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Artigo

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Wedi'i Gadw mewn:
12

Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt s... gan Zakia A. Abdelhamed, Gabrielle Wheway, Katarzyna Szymańska, Subaashini Natarajan, Carmel Toomes, Chris F. Inglehearn, Colin A. Johnson

Cyhoeddwyd 2013

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Artigo

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Wedi'i Gadw mewn:
13

The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway gan Zakia A. Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, C.F. Inglehearn, Carmel Toomes, Colin A. Johnson, Daniel J. Jagger

Cyhoeddwyd 2015

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Artigo

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Wedi'i Gadw mewn:
14

Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton gan Helen R. Dawe, Matthew Adams, Gabrielle Wheway, Katarzyna Szymańska, Clare V. Logan, Angelika A. Noegel, Keith Gull, Colin A. Johnson

Cyhoeddwyd 2009

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Artigo

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Wedi'i Gadw mewn:
15

Molecular cloning and chromosome mapping of the human gene encoding protein phosphotyrosyl phosphatase 1B. gan Sheryl Brown‐Shimer, Karen A. Johnson, Jeanne B. Lawrence, Colin A. Johnson, Arthur M. Bruskin, NancyR. Green, David E. Hill

Cyhoeddwyd 1990

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Artigo

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Wedi'i Gadw mewn:
16

DNA Methylation Is Linked to Deacetylation of Histone H3, but Not H4, on the Imprinted Genes <i>Snrpn</i>and <i>U2af1-rs1</i> gan Richard I. Gregory, Tamzin E. Randall, Colin A. Johnson, Sanjeev Khosla, I. Hatada, Laura P. O’Neill, Bryan M. Turner, Robert Feil

Cyhoeddwyd 2001

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Artigo

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Wedi'i Gadw mewn:
17

IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment gan Thibaut Eguether, Jovenal T. San Agustin, Brian T. Keady, Julie A. Jonassen, Yinwen Liang, Richard Francis, Kimimasa Tobita, Colin A. Johnson, Zakia A. Abdelhamed, Cecilia Lo, Gregory J. Pazour

Cyhoeddwyd 2014

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Artigo

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Wedi'i Gadw mewn:
18

Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis gan Su Kyoung Kim, Asako Shindo, Tae Joo Park, Edwin C. Oh, Srimoyee Ghosh, Ryan S. Gray, Richard A. Lewis, Colin A. Johnson, Tania Attié‐Bitach, Nicholas Katsanis, John B. Wallingford

Cyhoeddwyd 2010

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Artigo

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Wedi'i Gadw mewn:
19

Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies gan Katarzyna Szymańska, Ian Berry, Clare V. Logan, Simon RR Cousins, Helen Lindsay, Hussain Jafri, Yasmin Raashid, Saghira Malik-Sharif, Bruce Castle, Mushtag Ahmed, Chris Bennett, Ruth Carlton, Colin A. Johnson

Cyhoeddwyd 2012

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Artigo

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Wedi'i Gadw mewn:
20

A Germline Mutation in BLOC1S3/Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8) gan Neil V. Morgan, Shanaz Pasha, Colin A. Johnson, John R. Ainsworth, Robin A.J. Eady, Ban B. Dawood, C McKeown, Richard C. Trembath, Jonathan T. Wilde, Steve P. Watson, Eamonn R. Maher

Cyhoeddwyd 2005

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Artigo

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Wedi'i Gadw mewn:

Canlyniadau Chwilio - Colin A. Johnson

Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes gan Colin A. Johnson

The transition zone: an essential functional compartment of cilia gan Katarzyna Szymańska, Colin A. Johnson

The Cilium: Cellular Antenna and Central Processing Unit gan Jarema Malicki, Colin A. Johnson

Ciliogenesis and the DNA damage response: a stressful relationship gan Colin A. Johnson, Spencer J. Collis

The role of primary cilia in the development and disease of the retina gan Gabrielle Wheway, David Parry, Colin A. Johnson

Recent advances in the molecular pathology, cell biology and genetics of ciliopathies gan Matthew Adams, Ursula M. Smith, Clare V. Logan, Colin A. Johnson

Deacetylase Activity Associates with Topoisomerase II and Is Necessary for Etoposide-induced Apoptosis gan Colin A. Johnson, Kay Padget, Caroline A. Austin, Bryan M. Turner

Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin Please gan Claire E. L. Smith, Alice V. R. Lake, Colin A. Johnson

Meckel–Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances gan Verity Hartill, Katarzyna Szymańska, Saghira Malik Sharif, Gabrielle Wheway, Colin A. Johnson

Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome gan Gabrielle Wheway, Zakia Abdelhamed, Subaashini Natarajan, Carmel Toomes, Chris F. Inglehearn, Colin A. Johnson

Human Class I Histone Deacetylase Complexes Show Enhanced Catalytic Activity in the Presence of ATP and Co-immunoprecipitate with the ATP-dependent Chaperone Protein Hsp70 gan Colin A. Johnson, Darren A. White, Jayne S. Lavender, Laura P. O’Neill, Bryan M. Turner

The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway gan Zakia A. Abdelhamed, Subaashini Natarajan, Gabrielle Wheway, C.F. Inglehearn, Carmel Toomes, Colin A. Johnson, Daniel J. Jagger

Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton gan Helen R. Dawe, Matthew Adams, Gabrielle Wheway, Katarzyna Szymańska, Clare V. Logan, Angelika A. Noegel, Keith Gull, Colin A. Johnson

Molecular cloning and chromosome mapping of the human gene encoding protein phosphotyrosyl phosphatase 1B. gan Sheryl Brown‐Shimer, Karen A. Johnson, Jeanne B. Lawrence, Colin A. Johnson, Arthur M. Bruskin, NancyR. Green, David E. Hill

DNA Methylation Is Linked to Deacetylation of Histone H3, but Not H4, on the Imprinted Genes <i>Snrpn</i>and <i>U2af1-rs1</i> gan Richard I. Gregory, Tamzin E. Randall, Colin A. Johnson, Sanjeev Khosla, I. Hatada, Laura P. O’Neill, Bryan M. Turner, Robert Feil

IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment gan Thibaut Eguether, Jovenal T. San Agustin, Brian T. Keady, Julie A. Jonassen, Yinwen Liang, Richard Francis, Kimimasa Tobita, Colin A. Johnson, Zakia A. Abdelhamed, Cecilia Lo, Gregory J. Pazour

Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis gan Su Kyoung Kim, Asako Shindo, Tae Joo Park, Edwin C. Oh, Srimoyee Ghosh, Ryan S. Gray, Richard A. Lewis, Colin A. Johnson, Tania Attié‐Bitach, Nicholas Katsanis, John B. Wallingford

A Germline Mutation in BLOC1S3/Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8) gan Neil V. Morgan, Shanaz Pasha, Colin A. Johnson, John R. Ainsworth, Robin A.J. Eady, Ban B. Dawood, C McKeown, Richard C. Trembath, Jonathan T. Wilde, Steve P. Watson, Eamonn R. Maher

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