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Journal of Cellular Biochemistry
|
January 1, 1994
Molecular physiology of the islet amyloid polypeptide (IAPP)/amylin gene in man, rat, and transgenic mice
J W Höppener, C Oosterwijk, K L van Hulst, et al.
Cancer Research
|
November 1, 1996
Somatic mutations of the RET proto-oncogene are not required for tumor development in multiple endocrine neoplasia type 2 (MEN 2) gene carriers
R M Landsvater, M J de Wit, R A Zewald, et al.
Henry Ford Hospital Medical Journal
|
January 1, 1992
Long-term follow-up in four large MEN 2 families in The Netherlands
C J Lips, M J Berends, J Brouwers-Smalbraak, et al.
Diabetes
|
May 1, 1994
Human islet amyloid polypeptide accumulates at similar sites in islets of transgenic mice and humans
E J de Koning, J W Höppener, J S Verbeek, et al.
Journal of Internal Medicine
|
October 1, 1995
Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium
L M Mulligan, D J Marsh, B G Robinson, et al.
Diabetologia
|
February 1, 1991
Non-linkage of the islet amyloid polypeptide gene with type 2 (non-insulin-dependent) diabetes mellitus
J T Cook, P P Patel, A Clark, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1987
Expression of the second calcitonin/calcitonin gene-related peptide gene in Ewing sarcoma cell lines
J W Höppener, P H Steenbergh, R J Slebos, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia
R M Hofstra, R H Sijmons, T Stelwagen, et al.
The Netherlands Journal of Medicine
|
October 1, 1990
Insulinomas in MEN-I patients: early detection and treatment of insulinomas in patients with the multiple endocrine neoplasia syndrome type-I
M Jadoul, H P Koppeschaar, M A Bax, et al.
American Journal of Human Genetics
|
February 1, 1993
The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred
R M Landsvater, A G Rombouts, G J te Meerman, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 149) with videos related to
Sort By:
Page
of 15
Journal of Cellular Biochemistry
|
January 1, 1994
Molecular physiology of the islet amyloid polypeptide (IAPP)/amylin gene in man, rat, and transgenic mice
J W Höppener, C Oosterwijk, K L van Hulst, et al.
Cancer Research
|
November 1, 1996
Somatic mutations of the RET proto-oncogene are not required for tumor development in multiple endocrine neoplasia type 2 (MEN 2) gene carriers
R M Landsvater, M J de Wit, R A Zewald, et al.
Henry Ford Hospital Medical Journal
|
January 1, 1992
Long-term follow-up in four large MEN 2 families in The Netherlands
C J Lips, M J Berends, J Brouwers-Smalbraak, et al.
Diabetes
|
May 1, 1994
Human islet amyloid polypeptide accumulates at similar sites in islets of transgenic mice and humans
E J de Koning, J W Höppener, J S Verbeek, et al.
Journal of Internal Medicine
|
October 1, 1995
Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium
L M Mulligan, D J Marsh, B G Robinson, et al.
Diabetologia
|
February 1, 1991
Non-linkage of the islet amyloid polypeptide gene with type 2 (non-insulin-dependent) diabetes mellitus
J T Cook, P P Patel, A Clark, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1987
Expression of the second calcitonin/calcitonin gene-related peptide gene in Ewing sarcoma cell lines
J W Höppener, P H Steenbergh, R J Slebos, et al.
The Journal of Investigative Dermatology
|
August 1, 1996
RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia
R M Hofstra, R H Sijmons, T Stelwagen, et al.
The Netherlands Journal of Medicine
|
October 1, 1990
Insulinomas in MEN-I patients: early detection and treatment of insulinomas in patients with the multiple endocrine neoplasia syndrome type-I
M Jadoul, H P Koppeschaar, M A Bax, et al.
American Journal of Human Genetics
|
February 1, 1993
The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred
R M Landsvater, A G Rombouts, G J te Meerman, et al.
Page
of 15