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Human Genetics
|
March 30, 2004
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome
B T Teh, V M Howell, C J Haven, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism
B T Teh, S Kytölä, F Farnebo, et al.
Oncogene
|
June 16, 2015
High-resolution profiling of histone h3 lysine 36 trimethylation in metastatic renal cell carcinoma
T H Ho, I Y Park, H Zhao, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
July 29, 1998
Expression and chromosomal localization of the Requiem gene
T G Gabig, C D Crean, A Klenk, et al.
Human Molecular Genetics
|
July 1, 1997
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1
I Lemmens, W J Van de Ven, K Kas, et al.
Leukemia
|
February 14, 2018
Oncogenic activation of JAK3-STAT signaling confers clinical sensitivity to PRN371, a novel selective and potent JAK3 inhibitor, in natural killer/T-cell lymphoma
M -L Nairismägi, M E Gerritsen, Z M Li, et al.
Nature Genetics
|
November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
J D Carpten, C M Robbins, A Villablanca, et al.
Leukemia
|
February 9, 2016
JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma
M-L Nairismägi, J Tan, J Q Lim, et al.
Page
of 13
Search research articles
Search
Showing results (121-130 of 128) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 128 results.
Human Genetics
|
March 30, 2004
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome
B T Teh, V M Howell, C J Haven, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 26, 1998
Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism
B T Teh, S Kytölä, F Farnebo, et al.
Oncogene
|
June 16, 2015
High-resolution profiling of histone h3 lysine 36 trimethylation in metastatic renal cell carcinoma
T H Ho, I Y Park, H Zhao, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
July 29, 1998
Expression and chromosomal localization of the Requiem gene
T G Gabig, C D Crean, A Klenk, et al.
Human Molecular Genetics
|
July 1, 1997
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1
I Lemmens, W J Van de Ven, K Kas, et al.
Leukemia
|
February 14, 2018
Oncogenic activation of JAK3-STAT signaling confers clinical sensitivity to PRN371, a novel selective and potent JAK3 inhibitor, in natural killer/T-cell lymphoma
M -L Nairismägi, M E Gerritsen, Z M Li, et al.
Nature Genetics
|
November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
J D Carpten, C M Robbins, A Villablanca, et al.
Leukemia
|
February 9, 2016
JAK-STAT and G-protein-coupled receptor signaling pathways are frequently altered in epitheliotropic intestinal T-cell lymphoma
M-L Nairismägi, J Tan, J Q Lim, et al.
Page
of 13