Ngā hua rapu kaituhi

1

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

I whakaputaina 2003

Whiwhi kuputuhi katoa
Revisão

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2

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

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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3

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

I whakaputaina 2016

Whiwhi kuputuhi katoa
Revisão

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4

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

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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5

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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6

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

I whakaputaina 2008

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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7

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

I whakaputaina 2001

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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8

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

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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9

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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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10

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

I whakaputaina 2013

Whiwhi kuputuhi katoa
Artigo

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

I whakaputaina 2002

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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13

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

I whakaputaina 2015

Whiwhi kuputuhi katoa
Artigo

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14

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

I whakaputaina 2009

Whiwhi kuputuhi katoa
Artigo

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15

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

I whakaputaina 1990

Whiwhi kuputuhi katoa
Artigo

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

I whakaputaina 2001

Whiwhi kuputuhi katoa
Artigo

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17

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

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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18

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

I whakaputaina 2010

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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19

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

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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20

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

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Colin A. Johnson

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

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

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

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

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

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

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

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