The Community Guide

- gsearch

Search Results

Narrow Results:

2023 2
2022 1
2012 1

Journal Article 4

1 - 4 of 4 Results

Refine Results

Refine Results:

An Interferon-Related Signature in the Transcriptional Core Response of Human Macrophages to Mycobacterium tuberculosis Infection

CITE Title : An Interferon-Related Signature in the Transcriptional Core Response of Human Macrophages to Mycobacterium tuberculosis Infection Personal Author(s) : Wu, Kang;Dong, Dandan;Fang, Hai;Levillain, Florence;Jin, Wen;Mei, Jian;Gicquel, Brigitte;Du, Yanzhi;Wang, Kankan;Gao, Qian;Neyrolles, Olivier;Zhang, Ji; Published Date : Jun 04 2012 Source : PLoS One. 2012; 7(6). URL : https://stacks.cdc.gov/view/cdc/8202 Wu, Kang et al. (2012). An Interferon-Related Signature in the Transcriptional Core Response of Human Macrophages to Mycobacterium tuberculosis Infection. 7(6). Wu, Kang et al. "An Interferon-Related Signature in the Transcriptional Core Response of Human Macrophages to Mycobacterium tuberculosis Infection" 7, no. 6 (2012) Wu, Kang et al. "An Interferon-Related Signature in the Transcriptional Core Response of Human Macrophages to Mycobacterium tuberculosis Infection" vol. 7, no. 6, 2012 Export RIS Citation Information.

:

Wu, Kang ;

Dong, Dandan

Jun 04 2012 | PLoS One. 2012; 7(6).

:

The W-Beijing family of Mycobacterium tuberculosis (Mtb) strains is known for its high-prevalence and -virulence, as well as for its genetic diversity...
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

CITE Title : Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference? Personal Author(s) : Diaz Perez, Kimberly K.;Chung, Sydney;Taylor Head, S.;Epstein, Michael P.;Hecht, Jacqueline T.;Wehby, George L.;Weinberg, Seth M.;Murray, Jeffrey C.;Marazita, Mary L.;Leslie, Elizabeth J.; Published Date : 10 2023;10-2023; Source : Am J Med Genet A. 191(10):2558-2570 URL : https://stacks.cdc.gov/view/cdc/133514 Diaz Perez, Kimberly K. et al. (2023). Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?. 191(10). Diaz Perez, Kimberly K. et al. "Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?" 191, no. 10 (2023) Diaz Perez, Kimberly K. et al. "Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?" vol. 191, no. 10, 2023 Export RIS Citation Information.

:

Diaz Perez, Kimberly K. ;

Chung, Sydney

10 2023 | Am J Med Genet A. 191(10):2558-2570

:

Exome sequencing (ES) is now a relatively straightforward process to identify causal variants in Mendelian disorders. However, the same is not true fo...
Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

CITE Title : Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting Personal Author(s) : Perez, Kimberly K. Diaz;Curtis, Sarah W.;Sanchis-Juan, Alba;Zhao, Xuefang;Head, Taylor;Ho, Samantha;Carter, Bridget;McHenry, Toby;Bishop, Madison R.;Valencia-Ramirez, Luz Consuelo;Restrepo, Claudia;Hecht, Jacqueline T.;Uribe, Lina Moreno;Wehby, George;Weinberg, Seth M.;Beaty, Terri H.;Murray, Jeffrey C.;Feingold, Eleanor;Marazita, Mary L.;Cutler, David J.;Epstein, Michael P.;Brand, Harrison;Leslie, Elizabeth J.; Published Date : 10 2023;10-2023; Source : Genet Med. 25(10):100918 URL : https://stacks.cdc.gov/view/cdc/134539 Perez, Kimberly K. Diaz et al. (2023). Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting. 25(10). Perez, Kimberly K. Diaz et al. "Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting" 25, no. 10 (2023) Perez, Kimberly K. Diaz et al. "Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting" vol. 25, no. 10, 2023 Export RIS Citation Information.

:

Perez, Kimberly K. Diaz ;

Curtis, Sarah W.

10 2023 | Genet Med. 25(10):100918

:

Purpose:Orofacial clefts (OFCs) are common birth defects including cleft lip (CL), cleft lip and palate (CLP), and cleft palate (CP). OFCs have hetero...
Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes

CITE Title : Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes Personal Author(s) : Mukhopadhyay, Nandita;Feingold, Eleanor;Moreno-Uribe, Lina;Wehby, George;Valencia-Ramirez, Luz Consuelo;Muñeton, Claudia P. Restrepo;Padilla, Carmencita;Deleyiannis, Frederic;Christensen, Kaare;Poletta, Fernando A.;Orioli, Ieda M;Hecht, Jacqueline T.;Buxó, Carmen J.;Butali, Azeez;Adeyemo, Wasiu L.;Vieira, Alexandre R.;Shaffer, John R.;Murray, Jeffrey C.;Weinberg, Seth M.;Leslie, Elizabeth J.;Marazita, Mary L.; Published Date : 4 2022;4-2022; Source : Genet Epidemiol. 46(3-4):182-198 URL : https://stacks.cdc.gov/view/cdc/117318 Mukhopadhyay, Nandita et al. (2022). Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes. 46 Mukhopadhyay, Nandita et al. "Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes" 46 (2022) Mukhopadhyay, Nandita et al. "Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes" vol. 46, 2022 Export RIS Citation Information.

:

Mukhopadhyay, Nandita ;

Feingold, Eleanor

4 2022 | Genet Epidemiol. 46(3-4):182-198

:

Nonsyndromic orofacial clefts (OFCs) are among the most common craniofacial birth defects worldwide, and known to exhibit phenotypic and genetic hete...