Iskani rezultati za avtorja

1

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

Izdano 2003

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

Izdano 2012

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

Izdano 2016

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

Izdano 2016

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

Izdano 2013

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

Izdano 2008

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

Izdano 2001

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

Izdano 2020

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

Izdano 2017

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

Izdano 2013

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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 od Colin A. Johnson, Darren A. White, Jayne S. Lavender, Laura P. O’Neill, Bryan M. Turner

Izdano 2002

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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... od Zakia A. Abdelhamed, Gabrielle Wheway, Katarzyna Szymańska, Subaashini Natarajan, Carmel Toomes, Chris F. Inglehearn, Colin A. Johnson

Izdano 2013

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

Izdano 2015

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

Izdano 2009

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15

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

Izdano 1990

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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> od Richard I. Gregory, Tamzin E. Randall, Colin A. Johnson, Sanjeev Khosla, I. Hatada, Laura P. O’Neill, Bryan M. Turner, Robert Feil

Izdano 2001

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IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment od 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

Izdano 2014

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18

Planar Cell Polarity Acts Through Septins to Control Collective Cell Movement and Ciliogenesis od 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

Izdano 2010

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Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies od 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

Izdano 2012

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20

A Germline Mutation in BLOC1S3/Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8) od 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

Izdano 2005

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Rezultati - Colin A. Johnson

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

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

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

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

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

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

Deacetylase Activity Associates with Topoisomerase II and Is Necessary for Etoposide-induced Apoptosis od 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 od Claire E. L. Smith, Alice V. R. Lake, Colin A. Johnson

Meckel–Gruber Syndrome: An Update on Diagnosis, Clinical Management, and Research Advances od 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 od 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 od 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 od 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 od 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. od 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> od 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 od 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 od 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) od 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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