Works matching IS 00034800 AND DT 2018 AND VI 82 AND IP 3

Results: 8

The association of RAR‐related orphan receptor A (<italic>RORA</italic>) gene polymorphisms with the risk of asthma.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 158, doi. 10.1111/ahg.12238

By:

Cai, Xulong;
Lin, Mali;
Cao, Shan;
Liu, Yunguang;
Lin, Na

Publication type:

Article

A novel mutation in the <italic>HPGD</italic> gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 171, doi. 10.1111/ahg.12239

By:

Khan, Anwar Kamal;
Muhammad, Noor;
Khan, Sher Alam;
Ullah, Waheed;
Nasir, Abdul;
Afzal, Sibtain;
Ramzan, Khushnooda;
Basit, Sulman;
Khan, Saadullah

Publication type:

Article

<italic>p.X654R IDUA</italic> variant among Thai individuals with intermediate mucopolysaccharidosis type I and its residual activity as demonstrated in COS‐7 cells.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 150, doi. 10.1111/ahg.12236

By:

Ngiwsara, Lukana;
Ketudat‐Cairns, James R.;
Sawangareetrakul, Phannee;
Charoenwattanasatien, Ratana;
Champattanachai, Voraratt;
Kuptanon, Chulaluck;
Pangkanon, Suthipong;
Tim‐Aroon, Thipwimol;
Wattanasirichaigoon, Duangrurdee;
Svasti, Jisnuson

Publication type:

Article

The <italic>RSPO3</italic> gene as genetic markers for bone mass assessed by quantitative ultrasound in a population of young adults.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 143, doi. 10.1111/ahg.12235

By:

Correa‐Rodríguez, María;
Schmidt Rio‐Valle, Jacqueline;
Rueda‐Medina, Blanca

Publication type:

Article

Expression of miRNA‐146a, miRNA‐155, IL‐2, and TNF‐α in inflammatory response to <italic>Helicobacter pylori</italic> infection associated with cancer progression.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 135, doi. 10.1111/ahg.12234

By:

Zabaglia, Luanna Munhoz;
Sallas, Mayara Luciana;
Santos, Mônica Pezenatto Dos;
Orcini, Wilson Aparecido;
Peruquetti, Rita Luiza;
Constantino, Dulce Helena;
Chen, Elizabeth;
Smith, Marilia De Arruda Cardoso;
Payão, Spencer‐Luiz Marques;
Rasmussen, Lucas Trevizani

Publication type:

Article

A novel homozygous variant in <italic>BMPR1B</italic> underlies acromesomelic dysplasia Hunter–Thompson type.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 129, doi. 10.1111/ahg.12233

By:

Ullah, Asmat;
Umair, Muhammad;
Muhammad, Dost;
Bilal, Muhammad;
Lee, Kwanghyuk;
Leal, Suzanne M.;
Ahmad, Wasim

Publication type:

Article

A new association between <italic>CDK5RAP2</italic> microcephaly and congenital cataracts.

Published in:

Annals of Human Genetics, 2018, v. 82, n. 3, p. 165, doi. 10.1111/ahg.12232

By:

Alfares, Ahmed;
Alhufayti, Ibtihal;
Alsubaie, Lamia;
Alowain, Mohammed;
Almass, Rawan;
Alfadhel, Majid;
Kaya, Namik;
Eyaid, Wafaa

Publication type:

Article

Issue Information.

Published in:: Annals of Human Genetics, 2018, v. 82, n. 3, p. 1, doi. 10.1111/ahg.12216
Publication type:: Article