Summary of nucleotide variants in TD genes, characteristics and clinical manifestations.

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.

Amir Mehrvarz Sarshekeh (3818302)
Shailesh Advani (3818278)
Michael J. Overman (420496)
Ganiraju Manyam (2227252)
Bryan K. Kee (3818296)
David R. Fogelman (3818293)
Arvind Dasari (3818299)
Kanwal Raghav (3172167)
Eduardo Vilar (3818287)
Shanequa Manuel (3818290)
Imad Shureiqi (3818281)
Robert A. Wolff (678664)
Keyur P. Patel (3818284)
Raja Luthra (774811)
Kenna Shaw (3536021)
Cathy Eng (470950)
Dipen M. Maru (2282683)
Mark J. Routbort (3818305)
Funda Meric-Bernstam (478258)
Scott Kopetz (217667)

March 2017

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.</p

Summary for the association study of the subtypes on mutation level (top table) and gene level (bottom table).

Yang Liu (4829)
Qianchan He (5924636)
Wei Sun (93580)

November 2018

Summary for the association study of the subtypes on mutation level (top table) and gene level (bott...

Variants found in the present study and clinical characteristics of the families.

Maria Bejerholm Christensen (6645749)
Karin Wadt (447687)
Uffe Birk Jensen (395267)
Charlotte Kvist Lautrup (6645752)
Anders Bojesen (447688)
Lotte Nylandsted Krogh (489128)
Thomas van Overeem Hansen (4759692)
Anne-Marie Gerdes (395264)

April 2019

Variants found in the present study and clinical characteristics of the families.</p

Summary of nucleotide variants in DH genes, characteristics and clinical manifestations.

Nina Makretskaya (5778398)
Olga Bezlepkina (5778401)
Anna Kolodkina (5778404)
Alexey Kiyaev (5778407)
Evgeny V. Vasilyev (5778410)
Vasily Petrov (5778413)
Svetlana Kalinenkova (5778416)
Oleg Malievsky (5778419)
Ivan I. Dedov (627515)
Anatoly Tiulpakov (5778422)

September 2018

Summary of nucleotide variants in DH genes, characteristics and clinical manifestations.</p

Description of genetic variants related to T2D examined in the present study.

Gagandeep Kaur Walia (8374872)
Pratiksha Sharma (17027668)
Tripti Agarwal (2173453)
Moti Lal (17027671)
Himanshu Negandhi (3517379)
Dorairaj Prabhakaran (102287)
Rajesh Khadgawat (6834278)
Mohinder Pal Sachdeva (14333987)
Vipin Gupta (102192)

September 2023

Description of genetic variants related to T2D examined in the present study.</p

Nucleotide variant information for re-sequencing projects conducted in current study.

Jason W. Sahl (276694)
Christopher J. Allender (189556)
Rebecca E. Colman (254707)
Katy J. Califf (710313)
James M. Schupp (193214)
Bart J. Currie (131288)
Kristopher E. Van Zandt (710314)
H. Carl Gelhaus (710315)
Paul Keim (69765)
Apichai Tuanyok (78029)

March 2015

Nucleotide variant information for re-sequencing projects conducted in current study.</p

List of nucleotide variants from exome data which showed autosomal recessive inheritance model in consanguineous celiac disease family.

Jumana Yousuf Al-Aama (4025615)
Noor Ahmad Shaik (704629)
Babajan Banaganapalli (704628)
Mohammed A. Salama (4025624)
Omran Rashidi (4025627)
Ahmed N. Sahly (4025636)
Mohammed O. Mohsen (4025630)
Harbi A. Shawoosh (4025621)
Hebah Ahmad Shalabi (4025642)
Mohammad Al Edreesi (4025618)
Sameer E. Alharthi (4025639)
Jun Wang (5906)
Ramu Elango (704627)
Omar I. Saadah (4025633)

May 2017

List of nucleotide variants from exome data which showed autosomal recessive inheritance model in...

Summary of nucleotide mutations and the corresponding changes in the amino acids in RRDR loci (81 nucleotides, amino acids 426 to 452).

Priyanka Agrawal (721285)
Sandeep Miryala (721286)
Umesh Varshney (195227)

April 2015

The nucleotide mutations, corresponding amino acid changes and the frequency of occurrence of mut...

Nucleotide frequencies of TSD and its flanking sequences of complete elements (n = 59) and solo-LTRs (n = 112) of PbTRIM family.

Yihong Zhou (106947)
Sara Helms Cahan (106948)

December 2012

Nucleotide frequencies of TSD and its flanking sequences of complete elements (n = 59) and solo-L...

Genotypes of the three isolated clinical strains as determined using transfer RNA-linked short tandem repeats.

Yasuaki Yanagawa (3590654)
Shinji Izumiyama (10013539)
Yumiko Saito-Nakano (1842100)
Kumiko Nakada-Tsukui (181460)
Seiki Kobayashi (467790)
Naoko Yoshida (790080)
Yoshimi Kikuchi (212497)
Hiroyuki Gatanaga (205448)
Shinichi Oka (205454)
Tomoyoshi Nozaki (131314)
Koji Watanabe (205444)

September 2022

Genotypes of the three isolated clinical strains as determined using transfer RNA-linked short tande...

Summary of single nucleotide polymorphism types identified in three wheat genomes using the barley genome reference.

Hadi Alipour (6180281)
Guihua Bai (161677)
Guorong Zhang (3139737)
Mohammad Reza Bihamta (2825552)
Valiollah Mohammadi (6180284)
Seyed Ali Peyghambari (6180287)

January 2019

Summary of single nucleotide polymorphism types identified in three wheat genomes using the barley g...

Nucleotide and amino acid substitutions in the partial NS3 gene detected among Lithuanian TBEV strains.

Marina Sidorenko (17921530)
Jana Radzijevskaja (5467496)
Saulius Mickevičius (10894278)
Maksim Bratchikov (6688652)
Dalytė Mardosaitė-Busaitienė (5467493)
Povilas Sakalauskas (17921533)
Algimantas Paulauskas (5467499)

February 2024

Nucleotide and amino acid substitutions in the partial NS3 gene detected among Lithuanian TBEV strai...

Overview of the CYP2D6 allelic variants together with information regarding their relevance and impact on the enzyme.

Charleen G. Don (5675906)
Martin Smieško (4027895)

August 2018

Overview of the CYP2D6 allelic variants together with information regarding their relevance and impa...

Chromatogram showing the nucleotide sequence with the novel heterozygous missense mutation 536 C→A in WT1.

Xingru Li (385854)
Sihan Wang (385855)
Raviprakash T. Sitaram (285531)
Charlotta Andersson (385856)
Börje Ljungberg (72551)
Aihong Li (385857)

March 2013

Chromatogram showing the nucleotide sequence with the novel heterozygous missense mutation 536 C→...

Pathogenic and likely pathogenic variants by gene identified by the TruSight cancer sequencing panel.

Lorena Martin-Morales (5793827)
Paula Rofes (5793830)
Eduardo Diaz-Rubio (5793833)
Patricia Llovet (457407)
Victor Lorca (5793836)
Inmaculada Bando (303136)
Pedro Perez-Segura (5793839)
Miguel de la Hoya (238670)
Pilar Garre (457403)
Vanesa Garcia-Barberan (3147174)
Trinidad Caldes (3147195)

September 2018

Pathogenic and likely pathogenic variants by gene identified by the TruSight cancer sequencing panel...

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.

Amir Mehrvarz Sarshekeh (3818302)
Shailesh Advani (3818278)
Michael J. Overman (420496)
Ganiraju Manyam (2227252)
Bryan K. Kee (3818296)
David R. Fogelman (3818293)
Arvind Dasari (3818299)
Kanwal Raghav (3172167)
Eduardo Vilar (3818287)
Shanequa Manuel (3818290)
Imad Shureiqi (3818281)
Robert A. Wolff (678664)
Keyur P. Patel (3818284)
Raja Luthra (774811)
Kenna Shaw (3536021)
Cathy Eng (470950)
Dipen M. Maru (2282683)
Mark J. Routbort (3818305)
Funda Meric-Bernstam (478258)
Scott Kopetz (217667)

March 2017

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.</p

Summary for the association study of the subtypes on mutation level (top table) and gene level (bottom table).

Yang Liu (4829)
Qianchan He (5924636)
Wei Sun (93580)

November 2018

Summary for the association study of the subtypes on mutation level (top table) and gene level (bott...

Variants found in the present study and clinical characteristics of the families.

Maria Bejerholm Christensen (6645749)
Karin Wadt (447687)
Uffe Birk Jensen (395267)
Charlotte Kvist Lautrup (6645752)
Anders Bojesen (447688)
Lotte Nylandsted Krogh (489128)
Thomas van Overeem Hansen (4759692)
Anne-Marie Gerdes (395264)

April 2019

Variants found in the present study and clinical characteristics of the families.</p

Summary of nucleotide variants in DH genes, characteristics and clinical manifestations.

Nina Makretskaya (5778398)
Olga Bezlepkina (5778401)
Anna Kolodkina (5778404)
Alexey Kiyaev (5778407)
Evgeny V. Vasilyev (5778410)
Vasily Petrov (5778413)
Svetlana Kalinenkova (5778416)
Oleg Malievsky (5778419)
Ivan I. Dedov (627515)
Anatoly Tiulpakov (5778422)

September 2018

Summary of nucleotide variants in DH genes, characteristics and clinical manifestations.</p

Description of genetic variants related to T2D examined in the present study.

Gagandeep Kaur Walia (8374872)
Pratiksha Sharma (17027668)
Tripti Agarwal (2173453)
Moti Lal (17027671)
Himanshu Negandhi (3517379)
Dorairaj Prabhakaran (102287)
Rajesh Khadgawat (6834278)
Mohinder Pal Sachdeva (14333987)
Vipin Gupta (102192)

September 2023

Description of genetic variants related to T2D examined in the present study.</p

Nucleotide variant information for re-sequencing projects conducted in current study.

Jason W. Sahl (276694)
Christopher J. Allender (189556)
Rebecca E. Colman (254707)
Katy J. Califf (710313)
James M. Schupp (193214)
Bart J. Currie (131288)
Kristopher E. Van Zandt (710314)
H. Carl Gelhaus (710315)
Paul Keim (69765)
Apichai Tuanyok (78029)

March 2015

Nucleotide variant information for re-sequencing projects conducted in current study.</p

List of nucleotide variants from exome data which showed autosomal recessive inheritance model in consanguineous celiac disease family.

Jumana Yousuf Al-Aama (4025615)
Noor Ahmad Shaik (704629)
Babajan Banaganapalli (704628)
Mohammed A. Salama (4025624)
Omran Rashidi (4025627)
Ahmed N. Sahly (4025636)
Mohammed O. Mohsen (4025630)
Harbi A. Shawoosh (4025621)
Hebah Ahmad Shalabi (4025642)
Mohammad Al Edreesi (4025618)
Sameer E. Alharthi (4025639)
Jun Wang (5906)
Ramu Elango (704627)
Omar I. Saadah (4025633)

May 2017

List of nucleotide variants from exome data which showed autosomal recessive inheritance model in...

Summary of nucleotide mutations and the corresponding changes in the amino acids in RRDR loci (81 nucleotides, amino acids 426 to 452).

Priyanka Agrawal (721285)
Sandeep Miryala (721286)
Umesh Varshney (195227)

April 2015

The nucleotide mutations, corresponding amino acid changes and the frequency of occurrence of mut...

Nucleotide frequencies of TSD and its flanking sequences of complete elements (n = 59) and solo-LTRs (n = 112) of PbTRIM family.

Yihong Zhou (106947)
Sara Helms Cahan (106948)

December 2012

Nucleotide frequencies of TSD and its flanking sequences of complete elements (n = 59) and solo-L...

Genotypes of the three isolated clinical strains as determined using transfer RNA-linked short tandem repeats.

Yasuaki Yanagawa (3590654)
Shinji Izumiyama (10013539)
Yumiko Saito-Nakano (1842100)
Kumiko Nakada-Tsukui (181460)
Seiki Kobayashi (467790)
Naoko Yoshida (790080)
Yoshimi Kikuchi (212497)
Hiroyuki Gatanaga (205448)
Shinichi Oka (205454)
Tomoyoshi Nozaki (131314)
Koji Watanabe (205444)

September 2022

Genotypes of the three isolated clinical strains as determined using transfer RNA-linked short tande...

Summary of single nucleotide polymorphism types identified in three wheat genomes using the barley genome reference.

Hadi Alipour (6180281)
Guihua Bai (161677)
Guorong Zhang (3139737)
Mohammad Reza Bihamta (2825552)
Valiollah Mohammadi (6180284)
Seyed Ali Peyghambari (6180287)

January 2019

Summary of single nucleotide polymorphism types identified in three wheat genomes using the barley g...

Nucleotide and amino acid substitutions in the partial NS3 gene detected among Lithuanian TBEV strains.

Marina Sidorenko (17921530)
Jana Radzijevskaja (5467496)
Saulius Mickevičius (10894278)
Maksim Bratchikov (6688652)
Dalytė Mardosaitė-Busaitienė (5467493)
Povilas Sakalauskas (17921533)
Algimantas Paulauskas (5467499)

February 2024

Nucleotide and amino acid substitutions in the partial NS3 gene detected among Lithuanian TBEV strai...

Overview of the CYP2D6 allelic variants together with information regarding their relevance and impact on the enzyme.

Charleen G. Don (5675906)
Martin Smieško (4027895)

August 2018

Overview of the CYP2D6 allelic variants together with information regarding their relevance and impa...

Chromatogram showing the nucleotide sequence with the novel heterozygous missense mutation 536 C→A in WT1.

Xingru Li (385854)
Sihan Wang (385855)
Raviprakash T. Sitaram (285531)
Charlotta Andersson (385856)
Börje Ljungberg (72551)
Aihong Li (385857)

March 2013

Chromatogram showing the nucleotide sequence with the novel heterozygous missense mutation 536 C→...

Pathogenic and likely pathogenic variants by gene identified by the TruSight cancer sequencing panel.

Lorena Martin-Morales (5793827)
Paula Rofes (5793830)
Eduardo Diaz-Rubio (5793833)
Patricia Llovet (457407)
Victor Lorca (5793836)
Inmaculada Bando (303136)
Pedro Perez-Segura (5793839)
Miguel de la Hoya (238670)
Pilar Garre (457403)
Vanesa Garcia-Barberan (3147174)
Trinidad Caldes (3147195)

September 2018

Pathogenic and likely pathogenic variants by gene identified by the TruSight cancer sequencing panel...

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.

Amir Mehrvarz Sarshekeh (3818302)
Shailesh Advani (3818278)
Michael J. Overman (420496)
Ganiraju Manyam (2227252)
Bryan K. Kee (3818296)
David R. Fogelman (3818293)
Arvind Dasari (3818299)
Kanwal Raghav (3172167)
Eduardo Vilar (3818287)
Shanequa Manuel (3818290)
Imad Shureiqi (3818281)
Robert A. Wolff (678664)
Keyur P. Patel (3818284)
Raja Luthra (774811)
Kenna Shaw (3536021)
Cathy Eng (470950)
Dipen M. Maru (2282683)
Mark J. Routbort (3818305)
Funda Meric-Bernstam (478258)
Scott Kopetz (217667)

March 2017

Comparison of the incidences of SMAD4 mutations across different molecular subtypes.</p

Summary for the association study of the subtypes on mutation level (top table) and gene level (bottom table).

Yang Liu (4829)
Qianchan He (5924636)
Wei Sun (93580)

November 2018

Summary for the association study of the subtypes on mutation level (top table) and gene level (bott...

Variants found in the present study and clinical characteristics of the families.

Maria Bejerholm Christensen (6645749)
Karin Wadt (447687)
Uffe Birk Jensen (395267)
Charlotte Kvist Lautrup (6645752)
Anders Bojesen (447688)
Lotte Nylandsted Krogh (489128)
Thomas van Overeem Hansen (4759692)
Anne-Marie Gerdes (395264)

April 2019

Variants found in the present study and clinical characteristics of the families.</p

Summary of nucleotide variants in TD genes, characteristics and clinical manifestations.

Abstract

Extracted data

Summary of nucleotide variants in TD genes, characteristics and clinical manifestations.

Abstract

Extracted data

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