HOLT-ORAM SYNDROME; HOS

Literature (6)

Literature for OMIM 142900: HOLT-ORAM SYNDROME; HOS

Xenbase Articles:
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Denotes literature images)

Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome., He Ml,Campbell CE,Wu JY,Rao Y,Wen L, Proc Natl Acad Sci U S A. August 31, 1999; 96(18):1091-6490.
Lessons from the lily pad: Using Xenopus to understand heart disease., Bartlett HL,Weeks DL, Drug Discov Today Dis Models. January 1, 2008; 5(3):1740-6757.
Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development., Steimle JD,Slagle CE,Bekeny J,Rydeen AB,Kweon J,Yang XH,Ikegami K,Nadadur RD,Hoffmann AD,Lazarevic S,Thomas W,Luna-Zurita L,Ho RK,Kyba M,Zorn AM,Conlon FL,Moskowitz IP,Rankin SA,Rankin SA,Chan SS,Rowton M,Boyle Anderson EAT,Jensen B,Horb ME, Proc Natl Acad Sci U S A. November 6, 2018; 115(45):1091-6490.
Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD,Tandon P,Wilczewski CM,Wasson L,Herring LE,Venkatesh SS,Cristea IM,Conlon FL, PLoS Biol. September 1, 2019; 17(9):1545-7885.
Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia., Kariminejad A,Szenker-Ravi E,Lekszas C,Tajsharghi H,Moslemi AR,Naert T,Tran HT,Ahangari F,Rajaei M,Nasseri M,Haaf T,Azad A,Superti-Furga A,Maroofian R,Ghaderi-Sohi S,Najmabadi H,Abbaszadegan MR,Vleminckx K,Vleminckx K,Nikuei P,Reversade B, Am J Hum Genet. December 5, 2019; 105(6):1537-6605.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.

Transcription repression by Xenopus ET and its human ortholog TBX3, a gene involved in ulnar-mammary syndrome., He Ml,Campbell CE,Wu JY,Rao Y,Wen L, Proc Natl Acad Sci U S A. August 31, 1999; 96(18):1091-6490.

Lessons from the lily pad: Using Xenopus to understand heart disease., Bartlett HL,Weeks DL, Drug Discov Today Dis Models. January 1, 2008; 5(3):1740-6757.

Evolutionarily conserved Tbx5-Wnt2/2b pathway orchestrates cardiopulmonary development., Steimle JD,Slagle CE,Bekeny J,Rydeen AB,Kweon J,Yang XH,Ikegami K,Nadadur RD,Hoffmann AD,Lazarevic S,Thomas W,Luna-Zurita L,Ho RK,Kyba M,Zorn AM,Conlon FL,Moskowitz IP,Rankin SA,Rankin SA,Chan SS,Rowton M,Boyle Anderson EAT,Jensen B,Horb ME, Proc Natl Acad Sci U S A. November 6, 2018; 115(45):1091-6490.

Conservation and divergence of protein pathways in the vertebrate heart., Federspiel JD,Tandon P,Wilczewski CM,Wasson L,Herring LE,Venkatesh SS,Cristea IM,Conlon FL, PLoS Biol. September 1, 2019; 17(9):1545-7885.

Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia., Kariminejad A,Szenker-Ravi E,Lekszas C,Tajsharghi H,Moslemi AR,Naert T,Tran HT,Ahangari F,Rajaei M,Nasseri M,Haaf T,Azad A,Superti-Furga A,Maroofian R,Ghaderi-Sohi S,Najmabadi H,Abbaszadegan MR,Vleminckx K,Vleminckx K,Nikuei P,Reversade B, Am J Hum Genet. December 5, 2019; 105(6):1537-6605.

Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. May 1, 2024; 342(3):1552-5015.